Mycotoxins

Lyme, Mold and Mycotoxins: Strategies for Navigating Complex Illness

Darin Ingels, ND

SUmmary:

In the full presentation Lyme, Mold, and Mycotoxins: strategies for Navigating Complex Illness, Darin Ingels, ND, discusses the origin of Lyme Disease, how Lyme is spread, different ways to test for Lyme Disease and treat those affected by Lyme Disease.

Lyme Disease (LD) is among the more difficult of chronic syndromes – difficult to define, to diagnose and to treat. Since the mysterious outbreak of juvenile rheumatoid arthritis in the 1970s in Lyme, Connecticut, was first connected to microbial Borrelia burgdorferi spread by ticks, the understanding of these conditions has increased as Lyme itself has spread through the US and Europe.

Several species of ticks are expanding their range. The spread includes Canada, although Canada drastically underreports Lyme cases. Dr. Ingels provides considerable detail on Borrelia variants with maps documenting its relentless advance during the last few decades. He mentions that US variants have a stronger T-1 pro-inflammatory response, while European variants have a strong T-17 pro-inflammatory response.

Making identification of Lyme more difficult is the slow replication of Borrelia species (days instead of hours) and the organism’s ability to change shapes. The production of antibodies by Lyme sufferers isn’t dependable either. Many patients are entirely seronegative.

Laboratories often do not test for the full extent of the antibodies that have been associated with Lyme. The well-known bull’s-eye rash resulting from a tick bite is only present in 70% of patients according to the CDC, but other sources say 40%, and many Lyme sufferers have no recollection of a tick bite.

Symptoms are vague and overlap with other infectious and autoimmune conditions, which further confounds the problem of Lyme diagnosis. In children, confounding is even higher and symptoms include PANS and OCD.  Also, diseases such as tularemia may present similarly to Lyme.

Dr. Ingels points out that the CDC criteria for Lyme Disease was designed for surveillance purposes and do not necessarily reflect active infection with Borrelia species. The official diagnosis of Lyme Disease is a clinical diagnosis (signs and symptoms). The CDC warns against diagnosis of asymptomatic individuals, although it is possible to carry the microbes without symptoms. CDC-approved testing includes ELISA and Western blot: these are 40-year-old criteria.

ILADS (the International Lyme and Associated Disease Society) has more complex criteria for diagnosis of Lyme (LD) and coinfections. Their LD assessment approach includes a symptom questionnaire and suggested labs include hormones (thyroid, adrenal), nutritional (Vitamin D, minerals, amino acids), and immune markers as well as microbial coinfections. However, different laboratory tests may report markers for different microbial strains.

Dr. Ingels then segues into the involvement of mold as a major confounder of Lyme diagnosis. Mycotoxin toxic effects (mycotoxicosis) often overlap with Lyme Disease effects, and the damage both can do to the terrain also allows them to persist in a patient and contribute to ongoing oxidative stress and cell damage.

Fixing the terrain begins with – no surprise – healing the gut. Dr. Ingels offers the standard anti-inflammatory supplements such as probiotics and glutamine, and goes on to provide detailed diet guidance, emphasizing alkaline foods. The next step is to treat active infections, preferably with herbal supplements rather than antibiotics. He recommends several lesser-known herbal products for Lyme. Steps to reduce stress, improve sleep, and remove mold from the body and the environment are also presented. Treatment protocols should be tailored to each patient: “the best binder is the one your patient will take and tolerate’. Since sensitive mitochondria suffer “collateral damage” from these chronic conditions, Dr. Ingels winds up the lecture with mitochondria support supplements and detoxification strategies.

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Identifying and Treating Mold Toxin Induced Illness with MycoTOX Profile

SUMMARY:

In this presentation, James Neuenschwander, M.D., reviews some tell-tale signs of mold illness. He discusses the mechanisms by which mold toxins make patients ill and how a MycoTOX Profile helps identify these factors. Dr. Neuenschwander also provides practical protocols to remove patient barriers to healing of those suffering from mold or chronic illnesses.  

Before outlining a practical approach to treating mold illness patients, James Neuenschwander, M.D. provides a step-by-step description of the cellular response to toxins. The health information we consume frequently refers to “toxins” and “toxicity” without explaining how cellular processes are altered by toxic compounds. These cellular responses to toxins can manifest as the myriad and often baffling symptoms that chronic patients report.

He begins with the cell danger response (CDR), which triggers a cascade of cellular responses that may result in recycling of organelles or end in apoptosis of the cell itself. Apoptosis or “programmed cell death” is a normal process of growth and development, as well as a defense against pathogens. In a healthy state, cells are replaced, differentiated, and reconnected with neighboring cells.

Disease develops when the cellular healing process gets stuck; this can occur when mold and mycotoxin exposure is ongoing. Dr. Neuenschwander points out that if the host is sick, the host microbiome will also be out of balance and show signs of dysbiosis.

The full presentation includes the role of mitochondria, thought of primarily as energy producers, but which are very involved in the cellular response to stress. The presence of ATP outside the cell is part of cellular danger signaling, along with the appearance of various caspase enzymes at several points in the apoptosis process. The cell resorts to aerobic glycolysis, oxidative stress and glutamate level increase, and glutathione is diverted, vitamin D production drops, and methylation reactions are impaired.  Eventually, thyroid function is thrown off, and histamine increases. Patients with a chronic toxic load may develop MCAS and other indications of immune upregulation.

Dr. Neuenschwander mentions the myriad patient symptoms that can result from toxic processes instigated by mycotoxin exposure: psychiatric and cognitive symptoms, any chronic syndrome, respiratory symptoms, as well as POTS and other vagal symptoms. He uses Organic Acid Test (OAT) results as well as MycoTOX Profile results to illustrate possible responses to mycotoxins such as trichothecenes, aflatoxins, zearalenone, and ochratoxins. He also discusses the utility of specific immune and neurological testing.

An individual patient workup is included in this presentation and emphasis is placed on removal of mycotoxin exposure as determined by environmental testing. Food can also be a source of mycotoxins, particularly ochratoxin for which digestive binders are useful. Dr. Neuenschwander points out that unsprayed, organic food can often have higher mold content. He notes that the sickest patients have both mold colonization and an upregulated immune response to mycotoxin exposure and notes when antifungal treatment is called for.

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GPL improves health treatment outcomes for chronic illnesses by providing the most accurate, reliable, and comprehensive biomedical analyses available.

Workshop Q+A Part 2 - Mitochondria and Toxins

On August 5-7, 2022, GPL Academy hosted the Mitochondria and Toxins: Advanced Strategies & Protocols in Chicago and live-streamed online. The following Q+A is a grouping of responses from the workshop presentations.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


Joseph Pizzorno, N.D.

Joseph Pizzorno, ND is a world-leading authority on science-based natural medicine, a term he coined in 1978 as founding president of Bastyr University. A naturopathic physician, educator, researcher and expert spokesman, he is Editor-in-Chief of PubMed-indexed IMCJ, Chair of Board of IFM, board member of American Herbal Pharmacopeia, and a member of the science boards of the Hecht Foundation, Gateway for Cancer Research and Bioclinic Naturals. Author or co-author of six textbooks and 7 consumer books (Encyclopedia of Natural Medicine, The Toxin Solution), he has been an intellectual, political and academic leader in medicine for four decades.

Q: What was the supplement you recommended when using NAC for a patient?   

A: N-acetylcysteine is readily available from many good companies. I use Natural Factors/Bioclinic Natural since I am a scientific consultant for them. I like adding fiber to help bind the toxins that NAC helps excrete. 

Q: How do you detox arsenic? What nutrients or binders do you use to detox arsenic?  

A: The best detox for arsenic is avoidance. Its half-life is typically 2-4 days, so avoidance is effective. The rate of detox can be increased by consuming dietary folates, not folic acid, and flavonoids such as phloretin.  

Q: What are your thoughts on NAD and Glutathione IV therapy?  

A: IV therapy can be helpful but should only be done by those who are very skilled and when the safer oral interventions are not adequate. Before giving anyone IV glutathione, be sure the blood is cleared of mercury. 

Q: For someone with deletions in glutathione-S-transferase, what is the best way/form to increase GSH?  

A: This is really two different issues. Glutathione-S-transferase uses glutathione, does not produce it. Oral NAC and liposomal glutathione increase GSH. 

Q: With a sulfa allergy which is directly correlated with that deletion, is glutathione supplementation not recommended or cautioned?  

A: I am not aware of sulfa allergy being a contraindication for glutathione. 

Q: Is there any connection between the malate you are speaking about in your lecture and supplements with malate, such as calcium and magnesium malate?  

A: Same molecule. Several minerals have been bound to Krebs cycle intermediates, supposedly to improve absorption and utilization. 

Q: Do you have data on the effects of Metformin on Cplx 1 - causing acidosis?  

A: Yes, Metformin does indeed cause pericellular acidosis. Anything which increases lactic acidosis causes acidosis, such as biguanides (metformin), antiretrovirals, statins, many more. 


Elena Villanueva, D.C.

Dr. Elena Villanueva, producer and co-host of the 5 Part Series Mental Health Masterclass, the 5 Part Series Inflammation Masterclass, and The Leaky Brain Summit, is an internationally recognized crusader for ending the global chronic illness & mental health crisis by educating both the public and health professionals that mental health & other chronic illnesses are actually a body or brain health issue and not a disease. Elena has been featured on multiple occasions on FOX news, MSN, Healthline, Houston Chronicle, Anxiety and Depression Secrets Docu-Series, and several other documentaries. Dr Villanueva teaches on stages around the globe on evidence-based approaches for finding the underlying causes of chronic illness and brain-related conditions and how to use holistic and 'whole person' approaches to restore brain-related disorders and other chronic diseases.

 

Q: Do you have any experience with devices such as the NanoVi, to assist with mitochondrial function and proper folding of proteins? 

A: I do not. I do however have experience with bioenergetics and how that shows improvement of mitochondrial function. In fact, a recent study was just completed by a university out of California showing the biological improvements in mitochondrial function and replication with the use of bioenergetics. 

Q: What is your glyphosate protocol? 

A: Glyphosate has a short half-life and is one of the toxins that can leave the body without help of added supplementation. However, the client must discover and stop his/her exposure to the glyphosate for levels to come down. When we detox, our protocols are designed to detox ALL toxins, chemical, myco, and HM’s… this simplifies the protocols (and reduces the costs) for patients/clients and makes them much more compliant and with that compliance you and your patients/clients will see more consistent positive outcomes. 

Q: Are you concerned when toxins don't increase on testing between months 4-6 indicating they are not coming out as much? 

A: Not as much of a concern as it is an indicator that the client/patient is not compliant with the protocols. By month 4-6, if they are compliant with reducing their exposure and taking their recommended supplements and food protocols, you will see one of the following two scenarios: 

  1. Their toxins will show higher indicating they are releasing toxins from their body 

  2. Their toxins will show lower because they have already released a good portion of their toxic load quickly. 

If they are still showing the same levels after 3 months on deep detox, they are either still exposing themselves, not taking their protocols as recommended, or both. Keep in mind this is reflective for the protocols in our practice and may vary based on the protocols you establish. 

Q: For a colonized fungal infection in the gut do you cycle, rotate, or use one over-the-counter anti-fungal at a time? 

A: It depends. If the client/patient is not showing symptoms directly related to the fungal infection I focus instead on the broader picture with my deep detox protocols which also address fungal infections. If they are having considerable symptoms from the fungal infection, then yes, I put them on a fungal protocol first to mitigate their symptoms. Then I resume with my 12-month protocol system. 

Q: I have a 34-year-old female with extreme CFS, ADHD and depression for 12 years. Organic Acids Test results are within normal limits except for borderline high arabinose and low Vitamin C. MycoTOX Profile results are positive for ochratoxin A, citrinin, and chaet (from previous home). Dealing with severe debilitating brain fog, memory issues, poor executive function. She wants to go back on Adderall but worried that it will affect mitochondria/adrenals. Any insight on the negative effects of psychostimulants on CFS? 

A: We prefer to avoid those at all costs because of the negative side effects and potential damage they can have. If you are using effective protocols your client should be able to detox her mold toxins in an average of 9 months and you can include added brain and energy support during this time to help her… that could look like added high dose DHA, phospholipids, AA therapy, adrenal support, or even addressing vitamin and /or mineral deficiencies (according to labs) because those are common and can exacerbate brain fog, memory, etc. 

Q: Can you comment on use of Vitamin D with Vitamin K? Why do you use Vitamin K? 

A: High level overview on this: there are a percentage of people who have the VDR taq genetic variant and need Vitamin K to process their Vitamin D. Also, it simply ensures that the Vitamin D has the best chance at being utilized by the body. So, we are covering the bases without having to add more costly testing like genetic testing to their overall costs.  

Q: Just wondering the rationale for doing just the methyl B12/folate vs. a good B complex with activated forms? How do they replete the other B vitamins if given just the folate and B12? 

A: We do like using a good B complex with the methylated B12 and folate. However, at this time we have not found, nor have we been able to formulate a B complex that has the high therapeutic grade doses of methyl B12 methyl folate we prefer to use… therefore we use just the Methyl B12 and Methyl folate that we created in our brand at BioOne Sciences. There are some clients that we will put on additional B Complex. And all our clients that go into a year 2 program with us (which is most of them), get switched over to a B Complex (with the methylated B12 and Folate). We haven’t had an issue with repletion of the other B’s. 

Q: Could we get your pdf form for patients to record their lab results and significance? 

A: Please reach out to us at info@modernholistichealth.com We will be emailing our practitioners who are interested in learning our systems with information on our first live, in person training that we want to do and from that training we will share all our forms and protocols with you. 

Q: What is in your tox bundle? OAT, MycoTOX Profile, Heavy Metals and what else?  

A: Yes, those plus the environmental toxins and Glyphosate

Q: What was the biofilm agent you said you used?  

A: It’s our TCG Activation product that is humic/fulvic based.  

Q: Is it normal for a patient to get full body edema during a detox? 

A: No, it is not normal. It sounds like their detox pathways are not open and you should have your patient stop immediately. Be sure you check their blood labs for kidney and liver function, make sure they are having full evacuation bowel movements, and check for methylation challenges with some genetic testing. You might also get a history on any issues with their lymphatic system as well and determine if they have any allergies or sensitivities to any of the ingredients in the supplements you have them on. 


LEARN NEW WAYS TO HELP PATIENTS WITH DIFFICULT-TO-DIAGNOSE AND CHRONIC HEALTH ISSUES.

The tests discussed throughout each workshop are all used to help identify exposure sources and biochemical imbalances in individuals with chronic health conditions. The Organic Acids Test (OAT) contains multiple markers which may be influenced by environmental and mold toxins. Often, the combination of the OAT, MycoTOX Profile, and GPL-TOX Profile can be used to help identify how a patient might be getting exposed, as well as assist with correlating their symptoms back to these sources. Determining the underlying causes of chronic illnesses for patients is the key to integrative medicine, not just treating the symptoms. The Great Plains Laboratory continues to find new ways to detect these causes of many illnesses and study the correlations between the results and conditions.

Registration includes:

  1. Ability to purchase GPL tests discussed throughout the program at special workshop-only discounted rates.

  2. 60-day access to the full conference recordings.

  3. Permanent PDF access to each speaker’s slides.

  4. The option to purchase continuing education credits (5 credits per day), whether you attend in-person, watch Live Online, or watch the conference recordings at a later date! See detailed information about credits.

  5. An interactive Workshop Hub website where you can live chat and network with attendees and ask questions to the speakers.

  6. And last, but most certainly not least, qualified practitioners will receive a free OAT.

Workshop Q+A Part 1 - Mitochondria and Toxins

On August 5-7, 2022, GPL Academy hosted the Mitochondria and Toxins: Advanced Strategies & Protocols in Chicago and live-streamed online. The following Q+A is a grouping of responses from the workshop presentations.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


Kurt Woeller, D.O.

Kurt N. Woeller, D.O. has been an integrative medicine physician and biomedical Autism specialist for over 20+ years. He is an author of several health books including Autism – The Road To Recovery, Methyl-B12 Therapy For Autism, Methyl-B12 for Alzheimer’s Disease and Dementia, and 5 Things You MUST Do Right Now To Help With Your Rheumatoid Arthritis. He is an international speaker, educator, and practicing clinician offering specialized interventions for individuals with complex medical conditions. His health consulting practice for Autism alone is multinational with families from various countries. Dr. Woeller serves as a clinical and lab consult for Functional Medicine Clinical Rounds, as well as provides educational seminars for Great Plains Laboratory. He is co-founder of Integrative Medicine Academy (www.IntegrativeMedicineAcademy.com), which is an online training academy for health practitioners learning integrative medicine.

Q: How much more is covered in your Advanced OAT Mastery Course?

A: We go over every marker on the Organic Acids Test from Great Plains, as well as certain other markers commonly seen on other OATs.

Q: Do you ever delay addressing the bacterial/fungal dysbiosis to gently detox the patient first so that the removal of the biofilm is more effective and is only done once?

A: Yes, this can be done for some people.

Q: I have a patient who gets recurrent vaginal yeast infections monthly. She is told by her gynecologist that it’s hormonal. Could it be from a yeast/mold issue within the gut and environment? Should I run an Organic Acids Test on her?

A: Absolutely run an OAT.

Q: Do you typically avoid fungus plants in mold/mycotoxin patients? Do you use saccharomyces boulardii?

A: I use this from time to time. It can be helpful overall, but some people are sensitive to it.

Q: If the test shows candida or mold does that mean it is currently active?

A: On the OAT its active.  

Q: Or could it be showing that you did at one time have candida and there are antibodies or organic acids still present?

A: The IgG Food MAP can indicate past problems, but the OAT is current and active.

Q: Once you see the clostridia markers high on the OAT, do you run a stool test to confirm Clostridia presence before treating?

A: No, only unless they have significant bowel problems and want to rule out C. difficile with toxins and A and B.

Q: Polyethylene glycol is used widely in nursing homes for older people with constipation. It is also a component in some drugs and foods, how much of a health risk is this?

A: It’s a risk and certainly not ideal to use. There are many other options for constipation in the natural medicine world worth looking into.

Q: I understand, from other information I've viewed, that the OAT test can be hit-or-miss for oxalates because of cyclical excretion. Are you familiar with this phenomenon or its implications?

A: Yes. It’s called dumping. However, most of the time it is picked up on the OAT.

Q: For patients taking high doses of quercetin ascorbate (i.e. 2-8g/day) for mast cell hyperactivity, do you think there is a high probability of oxalate issues from such high doses of Vitamin C? Would a downward taper be a good idea, to avoid possible dumping when coming off it again?

A: Yes. Oxalates can manifest through this. For people who are very sensitive this would be a good idea. Not necessary for many people though.

Q: I've heard of good results with AURO topical glutathione. Your thoughts? Have you used it? vs Tri Fortify?

A: I have not used it.

Q: Would ADD medication affect the HVA value on the OAT?

A: Anything that drives up dopamine can affect the HVA value.

Q: What D-lactic free probiotics do you use/how do you know if the probiotic is D-lactic free?

A: It has to do with the type of bacteria in the probiotic. You will need to do some research on which bacteria produce D-lactic.

Q: Which marker on the OAT could indicate a coinfection of virus interfering with mitochondria function or getting damaged inducing the cell danger response?

A: There is no specific marker for viruses and no markers per se specific to the CDR.

Q: Do you have any thoughts or preferences on the form of CoQ10 to use, ie. Ubiquinol or Ubiquinone?

A: Ubiquinol.

Q: Do you have any thoughts on supplementing with Calcium Citrate for Oxalates and K2 amounts to address uptake? Does it matter if the Calcium is getting bound with the oxalates?

A: Vitamin K helps with bone mineralization so less availability for oxalate binding. It is a good idea to use too.

Q: Do molds that are known to be toxic that show up on the OAT not always produce toxins that would show up on the MycoTOX Profile?

A: Correct. There may not always be mycotoxins present, but they often are.

Q: Is Gliotoxin just produced by fungus or also candida?

A: There seems to be controversy around it, but it appears more likely that Candida can produce it too.

Q: Do you avoid using saccharomyces boulardii as an antifungal in those with fungal or mold related illness due to it being in that family of organisms, or do you find it still beneficial?

A: I do not use SB a lot. It can be helpful for some people, but watch out for reactions in people with inflammatory bowel disease.

Q: Can colonized molds create mycotoxins?

A: Yes

Q: Does the nephrotoxicity associated with ochratoxin, etc, tend to reverse once the detoxification has been done? 

A: It should if the problem has been more of a recent onset.

Q: Any experience using modified citrus pectin?

A: Some. It is another type of binder.

Q: At what level of a positive MycoTOX Profile do you treat mycotoxins? 

A: Any level outside the green. If its in the green than I mostly leave it alone unless the patient has known exposure and there is a high suspicion of mold/mycotoxin exposure.


James Greenblatt, M.D.

A pioneer in the field of integrative medicine, James M. Greenblatt, M.D., has treated patients since 1988. After receiving his medical degree and completing his psychiatry residency at George Washington University, Dr. Greenblatt completed a fellowship in child and adolescent psychiatry at Johns Hopkins Medical School. He currently serves as the Chief Medical Officer at Walden Behavioral Care in Waltham, MA and serves as an Assistant Clinical Professor of Psychiatry at Tufts University School of Medicine and Dartmouth College Geisel School of Medicine. Dr. Greenblatt has lectured internationally on the scientific evidence for nutritional interventions in psychiatry and mental illness.  He is the author of seven books, including Finally Focused: The Breakthrough Natural Treatment Plan for ADHD. He is the founder of Psychiatry Redefined, an educational platform dedicated to the transformation of psychiatry, which offers online CME-approved courses, webinars, and fellowships for professionals about functional and integrative medicine for mental illness. jgresources@gmail.com www.PsychiatryRedefined.org www.JamesGreenblattMD.com

Q: Do you think that the safety profile differs much between lithium carbonate, lithium citrate, and lithium orotate or are they all primarily dose-dependent?

A: I believe that the side effect profile is most often due to the amount of elemental lithium not the carrier model (i.e., Carbonate, citrate, or orotate). It is important to remember 150 mg of lithium carbonate only has 28 mg of elemental lithium.

Q: For patients with brain fog associated with long COVID, have you found Lithium helpful? Any protocols specific for long COVID?

A: Other than “the basics,” the most effective supportive supplements for long-haul COVID involve the use of lithium and OPC’s. Lithium (Lithium (Orotate) 1mg | Pure | Doctors and Patients Access (pureencapsulationspro.com) and Lithium (Orotate) 5mg | Pure | Doctors and Patients Access (pureencapsulationspro.com)) is recommended for patients with starting dose at 1-2 mg and titrate up if tolerated or needed to 5-10 mg. The OPC product is usually 2-3 times per day and we use the Curcumasorbmind (Cognitive Support Supplement* | Pure | Doctors and Patients Access (pureencapsulationspro.com)

Q: What kind of doses of lithium (or lithium levels) show the greatest effect on inflammation?

A: Using nutritional lithium for irritability, prevention of dementia, and neuroinflammation, we often use dosages that do not result in blood levels. There is very little research correlating blood levels with efficacy on any disorder except for bipolar disorder.

Q: It looks like some studies were done in the 90s showing “no effect” in OCD, but theoretically lowering neuro-inflammation would improve OCD. Have you seen any benefit of low dose lithium on PANS/PANDAS/OCD? How long would you trial it for in a pediatric patient before concluding it has no effect on them?

A: I have seen tremendous benefit in patients with PANS/PANDAS/OCD. I think the problem in our field is that we oversimplify our treatment response and simply assume every PANS/PANDAS/OCD patient with respond. As you know, there are multiple genetic and environmental factors that contribute to these illnesses and the exacerbation of symptoms. Lithium often plays a critical stabilizing role but without adequate testing and targeted treatments for the infection and other drivers of inflammation, lithium by itself is usually not enough.

Q: Is low lithium excretion on the urinary essential elements test equivalent to low lithium on hair mineral analysis?

A: I am not familiar with urine tests and am not convinced of utility of urine tests for assessment of lithium status. I know a few labs have developed these very quickly. I have not yet found them useful in clinical practice.

Q: Who offers lower than 5 mg dose in supplement form for Lithium?

A: Pure Encapsulations offers a 1 mg lithium orotate.

Q: What is the appropriate dosage for a suicidal person in an emergency and how soon will it calm the patient?

A: Any patient that is suicidal should be in an emergency room and low dose lithium is not an agent that is used for acute suicidal behavior.

Q: With the 1-2mg dosing in irritable children, is that 1-2mg of Lithium Orotate, or elemental?

A: Both. They should be the same. It should be elemental lithium, most commonly found as lithium orotate. For younger children under 6 years of age, I would recommend to start with 500 micrograms.

Q: How does lithium impact the Orotic marker on the OAT?

A: Lithium orotate simply will raise Orotic acid.

Q: Would there be any value in administering Lithium via IV?

A: I have not investigated IV lithium and, since lithium is so easily absorbed, it likely won’t be significantly advantageous.

Q: Can stress from living in a low social economic environment deplete lithium and require higher need?

A: Stress is unlikely to deplete lithium directly but all the related inflammatory markers and disruption in neurotransmitter utilization will likely require higher lithium.

Q: What are the parameters for dosing carbonate, as well as orotate in adults and then for children?

A: I can only share 150 mg lithium carbonate and 28 mg of lithium orotate. These should be dosed according to a physician’s clinical experience based on symptoms and underling diagnoses.

Q: What is the dosage range of lithium for generalized anxiety disorder?

A: I would recommend sticking to lower doses 1-5 mg.

Q: Which SNPs are related to higher lithium needs?

A: There are SNPs associated with lithium but not well understood. The only SNP that I consistently look at is BDNF.

Q: Would low dose lithium be acceptable for patient with Hashimoto’s and elevated levels of TSH when patient has Lithium deficiency?

A: I have utilized low doses of 2-5 mg with patients with thyroid disorder with good success, but this should be done carefully by monitoring thyroid function.

Q: Do you suggest Lithium carbonate or Lithium orotate with patient who is deficient?

A: Based on the dose, I usually use 1-20 mg lithium orotate. If I am looking for 30 mg or higher, I use lithium carbonate.

Q: What is dosage for adult female 115 lbs.?

A: Lithium is not dosed per body weight. We always start with 1-2 mg and titrate as we monitor symptoms and possible side effects.

Q: Would a thyme supplement be an alternative for lithium micro dosing?

A: I have not found that for any patients with clinical symptoms that herbal supplementation is sufficient.


LEARN NEW WAYS TO HELP PATIENTS WITH DIFFICULT-TO-DIAGNOSE AND CHRONIC HEALTH ISSUES.

The tests discussed throughout each workshop are all used to help identify exposure sources and biochemical imbalances in individuals with chronic health conditions. The Organic Acids Test (OAT) contains multiple markers which may be influenced by environmental and mold toxins. Often, the combination of the OAT, MycoTOX Profile, and GPL-TOX Profile can be used to help identify how a patient might be getting exposed, as well as assist with correlating their symptoms back to these sources. Determining the underlying causes of chronic illnesses for patients is the key to integrative medicine, not just treating the symptoms. The Great Plains Laboratory continues to find new ways to detect these causes of many illnesses and study the correlations between the results and conditions.

Registration includes:

  1. Ability to purchase GPL tests discussed throughout the program at special workshop-only discounted rates.

  2. 60-day access to the full conference recordings.

  3. Permanent PDF access to each speaker’s slides.

  4. The option to purchase continuing education credits (5 credits per day), whether you attend in-person, watch Live Online, or watch the conference recordings at a later date! See detailed information about credits.

  5. An interactive Workshop Hub website where you can live chat and network with attendees and ask questions to the speakers.

  6. And last, but most certainly not least, qualified practitioners will receive a free OAT.

Diagnosing Molds, Mycotoxins, and Things that Go Bump in the Night

SUMMARY

Mold is found in the environment and grows in water-damaged buildings. When exposed to mold and mycotoxins, patients will have no reaction, an allergic reaction, or a toxic reaction. Common toxic effects from mycotoxins include their ability to be neurotoxic, hepatotoxic, nephrotoxic, GI irritants, immune suppressant and modulating, skin irritants, hematologic toxins, carcinogenic, cardiovascular toxins, endocrine toxins, etc. This post discusses mold and mycotoxin exposure and recommends how a combination of diagnostic tools like the the Organic Acids Test, MycoTOX Profile, and the Mold IgE Allergy Test can guide your treatment.

By: Jasmyne Brown, N.D.

Functional medicine practitioners are not only healers but investigators of the root cause of runny eyes and noses. It’s our job to determine if a person’s allergic symptoms stem from seasonal triggers like grass and pollen or environmental triggers such as pet dander, mold, or mycotoxins. 

Mold and its mycotoxins seem to be ever present in the lives and sometimes the bodies of our clients. For some practitioners, mold and mycotoxins exposure and treatment may not have been taught during their training. So, what is mold exactly? Is it a yeast, a fungus or something completely different?  


Fungis, Molds, Yeasts, and Microorganisms that Cause Dysfunction 

In the animal kingdom, mold falls under the classification of fungi. These are eukaryotic microorganisms(3). Mold exists here along with yeasts and mushrooms (3). So indeed, it is a fungus making it closely related to yeasts like Candida. Unlike yeast, mold does not reproduce by budding. It reproduces by formation of multicellular hyphae via apical extension(4,6).  

Mold is found ubiquitously in the environment and found to grow in water-damaged buildings. Mold can contaminate foods that must be dried and stored, and mold is used in foods like in the production of cheese.  

Source: World Health Organization and Mycotoxins. Clinical microbiology reviews. Bennett, J. W., & Klich, M 

We’re constantly exposed to mold when we’re outdoors even though we can’t see it. Our forecasters tell us it’s there and how much of it is in the air during the evening weather forecasts. 

On days when the count is moderate to severe, we can see a rise in allergy-type symptoms in individuals with allergies.  

Another common source of mold exposure is from our diet. Certain foods are more prone to mold growth due to the way they are stored and/or grown. There are checks and balances that limit the number of mold/mycotoxins that are allowable before it is sent to market. This limits our exposure from food unless we overindulge in these foods. Common foods include coffee, grains, corn, dairy, wine, etc. Learn more about mold and mycotoxins in food here.  

Mold decomposes dead organic matter so it can grow on wood, the paper facing on gypsum board (drywall) and other materials made from wood. To grow, mold requires oxygen, heat and moisture. Due to this, mold commonly contaminates water damaged buildings. Materials often found to be contaminated include wallpaper, gypsum board, adhesives, pastes, and paints(1,5).  

Although it doesn't grow on non-organic matter like concrete and glass and metal, the dirt on these materials when in the right environment will allow for the growth of mold (1). This is where people get overly exposed to mold and its mycotoxins. The most common are Penicillium chrysogenum, Aspergillus versicolor, and Chaetomium globosum (1).  

When we get exposed to mold, we’ll either have no reaction, an allergic reaction, or a toxic reaction. In certain cases, we’ll experience both allergies and toxicity. So, what's the difference between an allergy and toxicity?   

How the Body Fights Back From Mold Exposure 

When an allergy is present, exposure to the offending substance or antigen triggers a response. This response is made by the immune system. In a true allergic situation, immunoglobulin E (IgE) antibodies are produced by the body. These IgE antibodies attack the antigen, in this case mold, and bind to cells like mast cells and basophils(7). This then triggers the release of chemical mediators like histamine. These chemicals are what induce the symptoms associated with allergies.   

Allergic reactions can also happen to common household molds rather than just molds that produce mycotoxins in water damaged spaces. Commonly people experience itchy watery eyes, sneezing, coughing, urticaria, sinusitis, asthma and wheezing, etc.(7) In sensitive individuals, whenever exposed to the antigen these symptoms will arise.  

During peak mold months in the summer and fall, you may be one of the millions of consumers combing your local drugstore for over-the-counter allergy medications and nasal sprays to find any relief from common allergens like pollen, and mold. You might also watch the weather forecast to prepare for the air quality and level of mold spore spikes in the air.  If you’re unfortunate enough to live in a water-damaged building, you can expect to see a chronic persistence of these allergic type symptoms.  

When Mold Exposure Elevates to a Chronic Illness 

Mold toxicity is different from mold allergy. In a toxicity, there is an over exposure to toxic metabolites that are produced by mold organisms. Toxicity states do not require immune mediated responses to be harmful or to cause what is experienced by the affected party.  

Mold toxins are considered mycotoxins. These compounds have activities that are harmful to humans, animals, and even other microorganisms. Their toxic nature includes neurotoxicity, nephrotoxicity, hepatotoxicity, immune dysregulation and suppressive properties, GI toxicity, cardio toxicity, carcinogenic, hematologic toxins, endocrine toxins, and more (2, 8).  

Myotoxicity has been referred to as the great masquerader in some scientific circles as it can present in many ways for different individuals. Exposure and symptomatology associated with mycotoxins is known as mycotoxicosis(2). It can be acute with a rapid onset that is clearly a large toxicity, or chronic which is a longer-term low-level exposure that usually results in cancers and more irreversible symptoms(2). 

Myotoxicity differs from mold allergy due to the lack of an immune mediated response. The symptoms you may experience from toxins are due to the toxic nature that they already have. An allergy, on the other hand, is the body’s immunologic response mounted to protect us from a foreign substance. Symptoms arise due to the degranulation of mast cells and basophils and the release of chemicals like histamines(7).  

This release is what causes allergic-like symptoms. In a pure toxicity state, you would not experience allergy symptoms. Also, someone without allergies could still feel the effect of mycotoxin overload, but wouldn’t suffer from congestion, itchy watery eyes etc. during allergy season. At least not from mold.  

When people are going through a toxicity state they are often dealing with an active exposure. This exposure is less likely due to the outside air alone, but maybe experienced in high outdoor air exposure rates. During high mold spore count months (summer and fall) those who compost, garden, forage, or do other activities in the soil, toxicity can be seen from these activities and situations(5).  

Though this is not what I commonly see. Water-damaged buildings and cars are the most common culprits for mold overexposure, in my experience. As said earlier, mold decomposes organic materials. Woods, wallpaper, and gypsum board are their fuel, due to the cellulose content, and happen to be extremely common building materials (1,5). When the mold is in ideal conditions it will grow in prominent levels and emit its toxic byproducts.  

Mold Affects Each Person Differently 

During large exposure levels toxicoses can occur. Various toxins can lead to different experiences, and individuality of people can lead to different manifestations. What does this mean? For example, you may have a stay-at-home mother and young child complaining of fatigue, anxiety, skin rash, ASD, GI issues etc., along with a partner and older child with no symptoms or mild fatigue or headache symptoms. Why is this?  

Usually, in these cases the mother and child spend an exponentially greater time in the moldy home than the older child and partner. As they may be going out of the home for work/school. There are also four different, yet similar, genetic make ups that allow for or do not allow for adequate detoxification and may make them more susceptible to the toxin’s effects.  

Situations also arise where the mold is concentrated in one person’s main living space that other family members do not frequent. Thus, increasing their exposure comparatively. All these factors are considered in mycotoxicosis. By understanding these differences and environmental spaces you can better pinpoint where the exposure is coming from.  

Common toxic effects from mycotoxins include their ability to be neurotoxic, hepatotoxic, nephrotoxic, GI irritants, immune suppressant and modulating, skin irritants, hematologic toxins, carcinogenic, cardiovascular toxins, endocrine toxins, etc. due to the wide range of effects and the endless toxic profile someone could present with, the manifestations that can occur are also endless and look different in each person (2). Because of this, looking into mold toxicity would be a good place to start or to rule out for someone with a chronic disease or a new onset of symptoms. 

Mold Exposure Diagnosis and Treatment 

Now that we understand the diverse ways mold can affect our bodies, are they interconnected in disease states? Of course, they are. It is common to see an allergic patient who also presents with a chronic disease or a new onset of symptoms. You may be dealing with a mold exposed client.  

On the other hand, these two manifestations of mold exposure can happen independent of each other. An allergic person not living or working in water damage can just have allergy symptoms. They wouldn't also present with toxic symptoms. This would also be limited to certain seasons when outdoor mold is higher. These individuals would also have significant relief in their home since mold is not growing there.  

In someone without an immune reaction, they would present with strictly toxic symptoms like fatigue, anxiety, pain, dizziness, headaches, etc. These would not be relieved while in the home/workplace/car and they may see relief when away from the exposure for a time.  

When you have someone come to you and you are thinking that they may be dealing with a mold issue, a combination of diagnostic tests can guide your treatment. When I suspect mold exposure, I like running the Organic Acids Test, MycoTOX Profile, and the Mold IgE Allergy Test. These three test will clarify what type of exposure you are dealing with. Is it toxicosis, allergies, or both. A full comprehensive mold workup includes all three of these reports.  

With this information, you will have better insight on what tools are needed to help heal your client from their mold exposure. Overall, an overexposure to mold can lead to two different experiences: allergic response and/or toxicity. When we understand how our clients respond to mold, we can better support them in their healing. 

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GPL improves health treatment outcomes for chronic illnesses by providing the most accurate, reliable, and comprehensive biomedical analyses available.


JASMYNE BROWN, N.D.

Jasmyne Brown is a board certified and licensed naturopathic doctor. She earned her Bachelor of Science in chemistry with a minor in biology from Alabama Agricultural and Mechanical University in 2013. Then she earned her Doctor of Naturopathic Medicine and Master of Human Nutrition degrees from the University of Bridgeport College of Naturopathic Medicine in 2017. Her professional training allows her to be able to interpret the GPL lab tests in a clinical manner, plus she enjoys identifying the biochemical pathways within our bodies and how nutrition and lifestyle impact them. Her educational background and her experience as a WIC nutritionist with the Florida Pasco County Department of Health allows her to convey complex concepts in a manner that can be grasped by anyone on multiple levels.


References  

  1. Andersen, B., Frisvad, J. C., Søndergaard, I., Rasmussen, I. S., & Larsen, L. S. (2011, June). Associations between fungal species and water-damaged building materials. Applied and environmental microbiology. Retrieved August 3, 2022, from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131638/ 
  2. Bennett, J. W., & Klich, M. (2003, July). Mycotoxins. Clinical microbiology reviews. Retrieved August 3, 2022, from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164220/ 
  3. Classification of animals: The complete guide. AZ Animals. (2022, February 19). Retrieved August 3, 2022, from https://a-z-animals.com/reference/animal-classification/ 
  4. Lakna. (2017, November 16). Difference between yeast and mold: Definition, structure, function, similarities. Pediaa.Com. Retrieved August 3, 2022, from https://pediaa.com/difference-between-yeast-and-mold/#:~:text=The%20main%20difference%20between%20yeast,of%20sexual%20or%20asexual%20spores. 
  5. Lstiburek, J., Brenna, T., & Yost, N. (2002, January 15). RR-0208: What you need to know about mold. Building Science Corporation. Retrieved August 3, 2022, from https://www.buildingscience.com/documents/reports/rr-0208-what-you-need-to-know-about-mold/view 
  6. McGinnis, M. R., & Tyring, S. K. (1996). Introduction to mycology - medical microbiology - NCBI bookshelf. National Library of Medicine. Retrieved August 3, 2022, from https://www.ncbi.nlm.nih.gov/books/NBK8125/ 
  7. Sánchez, P., Vélez-del-Burgo, A., Suñén, E., Martínez, J., & Postigo, I. (2022, March 9). Fungal allergen and mold allergy diagnosis: Role and relevance of Alternaria alternata alt a 1 protein family. MDPI. Retrieved August 3, 2022, from https://www.mdpi.com/2309-608X/8/3/277/html 
  8. World Health Organization. (n.d.). Mycotoxins. World Health Organization. Retrieved August 3, 2022, from https://www.who.int/news-room/fact-sheets/detail/mycotoxins#:~:text=Mycotoxins%20are%20naturally%20occurring%20toxins,under%20warm%20and%20humid%20conditions.  

Kidney: The Often-Forgotten Part of Detoxification

Quick glance

  • Toxicants can be absorbed via three main pathways: respiratory tract via inhalation, integumentary system via direct skin contact, or gastrointestinal tract (GI) via consumption (2).

  • Chemical toxicants passing through the kidneys can be measured in urine.

  • Included are recommendations that can be put in place to ensure your patients’ kidneys function well and are prepared to do the work of detoxification of any type of toxic intruder.

By: Lindsay Goddard, M.S., R.D.N., L.D.

Too often the liver and the GI tract are the first two organs that spring to mind when the word detoxification is mentioned.  Granted, these two systems do a lot of important work in removing toxins from the body, but another vital organ that detoxifies the body are the kidneys.

The kidneys are instrumental in detoxifying a wide range of end products of metabolism. Toxins which have gone through phase II liver detoxification or direct excretion, and excess water-soluble nutrients such as B vitamins and Vitamin C are also filtered out by the kidneys (1). The kidneys allow these compounds to be removed from the body via urine, which along with stool, is the major pathway of elimination. Sweat, tears, saliva, hair, nails, and milk, all are a part of elimination as well, but to a lesser degree (2). In this blog we will discuss the kidneys and the roles they play in elimination of toxins, especially ones found on the MycoTOX Profile and the GPL-TOX Profile.


How the Kidney Works

Let’s first review the kidney and its function. It is a complex, and sophisticated organ that is so important, nature felt two were necessary. These bean shaped organs have many functions, but one of the major roles is filtering out excess water and cleaning the blood from toxins. They are so efficient, they can clean all the blood in the body in just under an hour on average (3).

The three layers of the kidney are the cortex (outer layer), medulla (inner part), and the central pelvis. Unfiltered blood travels through the cortex via the renal artery into the nephron. The nephrons are basically the blood filtering units composed of bundles of blood vessels called glomerulus, within the Bowman capsules.

When the blood passes through the glomeruli, within the medulla, waste and excess water diffuse into the capsule. The excess is then carried away by tubules to form urine, while useful substances that can be recycled are absorbed by the capillaries. The filtered blood is sent back to the heart via the renal vein. The urine is then carried through the tubules to the central pelvis, which is then emptied into two tubes called ureters, ultimately going to the bladder (2).

To be fair, the kidneys have other notable functions as well, such as release of certain hormones, stimulation of red blood cell production, and supporting fluid homeostasis within the body, but those details are outside the scope of this blog.

Figure 1: Basic Structure of the Kidney. Adapted from the University of Michigan. http://websites.umich.edu/~elements/web_mod/viper/kidney_function.htm (4).


Eliminating Toxicants

How do toxicants enter our systems? Toxicants can be absorbed via three main pathways: respiratory tract via inhalation, integumentary system via direct skin contact, or gastrointestinal tract (GI) via consumption (2).

The pulmonary route of absorption can be quite significant as the lung tissue is highly vascularized and has a larger surface area. The GI tract also has a larger surface area, but pH has a greater influence on this systems ability to absorb.

The skin isn’t as permeable (unless there is an opening), and it’s mainly the lipid-soluble compounds that are the most worrisome, as they can be absorbed more efficiently via passive diffusion. In a very, very simplistic view, once the toxicant is absorbed via the skin or respiratory tract, it ultimately ends up in the blood where it can travel throughout the system.

The GI tract absorption is different in that if it passes through the membranes, it will likely pass through the liver before it enters general circulation. Ultimately, the body’s goal is to eliminate toxicants. As noted previously, urinary excretion via the kidney is an extremely important mechanism for this to occur.

When toxicants enter the kidney, a large amount are filtered across the glomerulus with relative ease if they are not protein bound in the plasma and/or are relatively small. Ionized toxicants tend to remain in the urine, while toxicants that are more lipophilic can re-enter renal circulation through reabsorption (2). This is the case with Ochratoxin A (OTA) from Great Plains Laboratory’s MycoTOX Profile.

OTA is quite nephrotoxic, and this is likely because as it is going through organic anion transport in the tubules of the kidney, it is actively being reabsorbed. It is also transported with smaller carrier proteins, allowing the compound to pass through the glomerular membrane at an increased rate (5-7). Other than OTA, there are other mycotoxins that can impact the kidneys while they pass through it.

Other Ochratoxins, particularly C, can be damaging to the kidney, though the direct mechanism of action is still being investigated (8). Mycotoxins from Fusarium and Aspergillus, particularly some of the aflatoxins (B2, G1, M1 and M2), and the T2 toxin have all been documented in literature to influence the kidneys during excretion (9-12).

Evidence also indicates that Gliotoxin has cytotoxicity to renal epithelial cells, even at lower concentrations (13). Verrucarin A and Roridin E have both been found to be highly absorbed into the kidneys, even more so than the liver or lungs (14, 15).

Mycophenolic Acid (MPA) goes through glucuronidation in the kidneys, and is mainly eliminated via urine by active tubular secretion and glomerular filtration (16-18). These mycotoxins are all measured on the GPL’s MycoTOX Profile, and can be a helpful clue into what assaults are occurring on the kidneys, along with the other added benefits of running a MycoTOX Profile.



Eliminating Chemical Toxicants

Chemical toxicants passing through the kidneys can be measured in urine. The structure of the chemical compound has a large influence on its excretion through the kidneys. The more lipophilic the compound, the more likely it will be reabsorbed, or in other words, have a difficult time eliminating. The more hydrophilic compounds are, the easier they are to eliminate (1,2).

Please do not think of chemicals that are easy to eliminate as not as toxic as others. Though they may not bioaccumulate as well, the damaging effects they can have while in the system prior to elimination are still of concern, especially with chronic exposure.

Saturation plays a factor in the kidney’s ability to eliminate, meaning it only has a certain capacity it can filter. Mitochondrial function can also be a factor since the ATP generated from the citric acid cycle can help actively move the toxicants out (1).

When you look at toxicants on the GPL-TOX Profile, one can get an idea of the more water-soluble compounds by the metabolite name. If the metabolite is the same name as the parent compound, then it did not have to go through much metabolism to be eliminated. Toxicants such as Diphenyl Phosphate, Perchlorate, and 2,4-Dichlorophenoxyacetic Acid (2,4-D) all fit that description. The others are more complex, and it gets even more complex with heavy metals, but we can save that for another blog.

How to Support the Kidneys

So, we now know what the kidneys do, and what assaults can negatively impact them, the next question  is how can I support it? How do we take care of the kidneys so they can do their job(s) well?

If you have been looking into the world of environmental toxins, it is abundantly clear that the most important thing to do is remove/reduce the toxicant loads. That is a whole other topic, and some really great blogs/webinars have been produced that already delve into mold testing for your body and your home as well as identifying toxins in your environment. If you don’t remove the source, no matter what you do, the problem will persist.



Additional Recommendations

Below are some additional recommendations that can be put in place to ensure our kidneys function well and are prepared to do the work of detoxification of any type of toxic intruder.

  1. Drinking enough clean water. Keeping fluid moving through the body and the kidneys will help them run efficiently and get the toxicants out quicker. There is no specific amount, as everyone is different, but a good general guideline is half the body weight in ounces (e.g. a 120lb person should consume around 60oz of water, minimum). Also, check the urine color to help. Too yellow means more water, clear urine means too much water, as it should have a tinge of yellow to it.

  2. Decrease Sodium and Phosphorus Intake. Sodium and Phosphorus in excessive amounts (not the kind in natural foods, rather the kind in processed foods) can cause imbalances in the kidneys and put additional strain on them, causing them to work harder.

  3. Movement. Improving blood and lymph flow through movement can help the kidneys function optimally. Walking, Yoga (added bonus with the breathing - that’s a part of detoxing too believe it or not!), bicycling, etc. Whatever movement brings joy, it will help.

  4. N-acetyl Cysteine (NAC). NAC has been known to protect kidneys from various assaults. A meta-analysis found that supplementation with NAC improved glomerular filtration rate and serum creatinine, indicating supportive effects (19).

  5. Functional Foods. Various foods can have direct effects on kidney improvement. Beets can support better blood flow throughout the system, in particular the kidneys (20). Blueberries and cabbage have been shown to help with reducing inflammation in the kidneys (21, 22). Curcumin has evidence suggesting it can be helpful in protecting the renal mitochondria (23). Cinnamon, although the effects are not directly towards the kidneys, can help control blood sugar which in turn helps support the kidneys (24).

  6. Be aware that some herbals can be toxic for the kidneys, while other herbs may have influences on kidney function, if the kidney is already in distress. Be mindful with herbal tinctures depending on the current state of the kidney (25).

There are other supports for the kidneys out there, but these should at least be a good start.

The kidneys are incredibly important in helping with the elimination of toxicants, and it is important to support them with lifestyle and diet. We need to support our bodies for the environment in which we live and take care of our systems to ensure they can work properly to withstand the challenges.

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GPL improves health treatment outcomes for chronic illnesses by providing the most accurate, reliable, and comprehensive biomedical analyses available.


Lindsay Goddard, M.S., R.D.N., L.D.

Lindsay Goddard is a Registered Dietitian, with a Master’s Degree in nutrition. She has been involved in integrative and functional nutrition for over 10 years. She has worked in a variety of specialty areas such as genetic and metabolic disorders along with NICU and pediatrics. She also had a private practice where she specialized in gastrointestinal disorders. Lindsay now works as a GPL consultant and is currently earning her graduate certificate in Toxicology through The University of South Florida.


References: 
  1. Pizzorno J. The Kidney Dysfunction Epidemic, Part 1: Causes. Integr Med (Encinitas). 2015 Dec;14(6):8-13. PMID: 26807064; PMCID: PMC4718206.
  2. Richards I and Bourgeois M. Principles and Practice of Toxicology in Public Health. 2014. ISBN: 9781449645267
  3. A, Fardon J, Friend J, Temple N, Routh, K. et al. The Amazing Body. Smithsonian. 2017. First American Edition. Pg. 154-155. ISBN: 978-1-4654-6239-8
  4. University of Michigan. Kidney Function. http://websites.umich.edu/~elements/web_mod/viper/kidney_function.htm
  5. Khoury A and Atoui A. Ochratoxin A: General Overview and Actual Molecular Status. Toxins. 2010. 2(4): 461-493. PMID: 22069596
  6. Gupta, Ramesh C. Veterinary Toxicology. Basic and Clinical Principles 3rd edition. 2018. 
  7. Plumlee KH. Mycotoxins Toxicokinetics. Clinical Veterinary Toxicology. 1st Edition. 2004
  8. Abramson D. MYCOTOXINS Toxicology. Encyclopedia of Food Microbiology. 1999. Pages 1539-1547. ISBN 9780122270703. https://doi.org/10.1006/rwfm.1999.1150.
  9. Mohan J, Sheik Abdul N, Nagiah S, Ghazi T, Chuturgoon AA. Fumonisin B2 Induces Mitochondrial Stress and Mitophagy in Human Embryonic Kidney (Hek293) Cells-A Preliminary Study. Toxins (Basel). 2022 Feb 25;14(3):171. doi: 10.3390/toxins14030171. PMID: 35324667; PMCID: PMC8954924.
  10. Coppock RW, Dziwenka MM. Mycotoxins. Biomarkers in Toxicology. 2014. Pages 549-562.ISBN 9780124046306. https://doi.org/10.1016/B978-0-12-404630-6.00032-4. https://www.sciencedirect.com/science/article/pii/B9780124046306000324. 
  11. Nassar AY, Megalla SE, El-Fattah HM, Hafez AH, El-Deap TS. Binding of aflatoxin B1, G1 and M to plasma albumin. Mycopathologia. 1982 Jul 23;79(1):35-8. doi: 10.1007/BF00636179. PMID: 6811900.
  12. Adhikari M, Negi B, Kaushik N, Adhikari A, Al-Khedhairy AA, Kaushik NK, Choi EH. T-2 mycotoxin: toxicological effects and decontamination strategies. Oncotarget. 2017 May 16;8(20):33933-33952. doi: 10.18632/oncotarget.15422. PMID: 28430618; PMCID: PMC5464924.
  13. Gayathri, L., Akbarsha, M. & Ruckmani, K. In vitro study on aspects of molecular mechanisms underlying invasive aspergillosis caused by gliotoxin and fumagillin, alone and in combination. Sci Rep 10, 14473 (2020). https://doi.org/10.1038/s41598-020-71367-2
  14. Amuzie CJ, Islam Z, Kim JK, Seo JH, Pestka JJ. Kinetics of satratoxin g tissue distribution and excretion following intranasal exposure in the mouse. Toxicol Sci. 2010;116(2):433-440. doi:10.1093/toxsci/kfq142
  15. Amuzie CJ, Islam Z, Kim JK, Seo JH, Pestka JJ. Kinetics of satratoxin g tissue distribution and excretion following intranasal exposure in the mouse. Toxicol Sci. 2010;116(2):433-440. doi:10.1093/toxsci/kfq142
  16. Food and Drug Association. Mycophenolic acid (Myfortic). https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/050791s002lbl.pdf
  17. Lamba V, Sangkuhl K, Sanghavi K, Fish A, Altman RB, and KE.PharmGKB. Mycophenolic Acid Pathway. Pharmacogenetics and genomics.2014. PMID:24220207. https://www.pharmgkb.org/pathway/PA165964832
  18. Hooijmaaijer E, Brandl M, Nelson J, Lustig D. Degradation products of mycophenolate mofetil in aqueous solution. Drug Dev Ind Pharm. 1999 Mar;25(3):361-5. doi: 10.1081/ddc-100102183. PMID: 10071831.
  19. Ye M, Lin W, Zheng J, Lin S. N-acetylcysteine for chronic kidney disease: a systematic review and meta-analysis. Am J Transl Res. 2021 Apr 15;13(4):2472-2485. PMID: 34017406; PMCID: PMC8129408.
  20. Kolluru GK, Kevil CG. Beets, bacteria, and blood flow: a lesson of three Bs. Circulation. 2012 Oct 16;126(16):1939-40. doi: 10.1161/CIRCULATIONAHA.112.136515. Epub 2012 Sep 19. PMID: 22992323; PMCID: PMC4078643.
  21. Nair AR, Masson GS, Ebenezer PJ, Del Piero F, Francis J. Role of TLR4 in lipopolysaccharide-induced acute kidney injury: protection by blueberry. Free Radic Biol Med. 2014 Jun;71:16-25. doi: 10.1016/j.freeradbiomed.2014.03.012. Epub 2014 Mar 19. PMID: 24657730.
  22. Asiwe JN, Kolawole TA, Anachuna KK, Ebuwa EI, Nwogueze BC, Eruotor H, Igbokwe V. Cabbage juice protect against lead-induced liver and kidney damage in male Wistar rat. Biomarkers. 2022 Mar;27(2):151-158. doi: 10.1080/1354750X.2021.2022210. Epub 2022 Jan 3. PMID: 34974788.
  23. Trujillo J, Chirino YI, Molina-Jijón E, Andérica-Romero AC, Tapia E, Pedraza-Chaverrí J. Renoprotective effect of the antioxidant curcumin: Recent findings. Redox Biol. 2013 Sep 17;1(1):448-56. doi: 10.1016/j.redox.2013.09.003. PMID: 24191240; PMCID: PMC3814973.
  24. Khan A, Safdar M, Ali Khan MM, Khattak KN, Anderson RA. Cinnamon improves glucose and lipids of people with type 2 diabetes. Diabetes Care. 2003 Dec;26(12):3215-8. doi: 10.2337/diacare.26.12.3215. PMID: 14633804.
  25. National Kidney Foundation. Use of Herbal Supplements in Chronic Kidney Disease. 2009. https://kidneyhi.org/use-of-herbal-supplements-in-chronic-kidney-disease/

Mycotoxin, Glyphosate & IgG: Q&A With Elena Villanueva, DC, Shanhong Lu, MD, William Shaw, PhD & Lindsay Goddard, RD

On June 10-12, 2022, GPL Academy hosted Beyond the Basics: Advanced Organic Acids Testing Strategies live-streamed online. This three-day event focused on advanced Organic Acids topics. Those who attended the summit learned how to use effective diagnostic and treatment protocols for their patients to help get them on the road to recovery.

The following Q+A is a grouping of responses from the Day 3 workshop presentations. Click each presentation title to expand the answers from each speaker.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


Day 3 Q+A: Toxin Exposure and More


William Shaw, PhD

Organic Acids and Mycotoxins: Correlations With Mold in Various Chronic Illnesses | Speaker Panel

Q: Why not add Volatile Organic Compounds to your MycoTOX Profile?

A: Volatile organics would have to be extracted by a different method than mycotoxins. 

 

 

Q: Farmed chickens are fed corn. Do you think chicken meat may contain mycotoxins?

A: Very likely, unless corn feed is tested for mycotoxins.

  

 

Q: Do you use 240 mg/kg/day to calculate the dosage of cholestyramine for children or how do you calculate pediatric dosage? Would you use cholestyramine in infants as well?

A: The usual dosage in children (0-17 years) is 240 mg/kg of body weight per day of anhydrous cholestyramine resin taken in 2 to 3 divided doses. Most children won’t need more than 8 grams per day.

 

 

Q: Which medication or herbal combinations are best for both Candida and Aspergillus simultaneously?

A: The big problem is that there is a lack of published studies for herbals used as antifungals. Amphotericin and itraconazole have been used for both Candida and many molds, but there are resistant strains that require other drugs.

 

 

Q: For children with liver toxicity due to Sporanox, how do you approach that? Maybe half dose for twice as long?  Do you have ideas for alternatives for Itraconazole/ Sporanox?

A: I would recommend oral nystatin, if there is evidence of liver toxicity with Sporanox. This is because nystatin is not absorbed from the GI tract.

 

 

Q: Why do some people get so sick when exposed to mold? Could it be the genetic component HLA gene possibly? 

A: All of the mycotoxins are extremely toxic and may be fatal. The dose of mycotoxin is likely the main factor determining the degree of illness. Neil Nathan, MD states that he found HLA testing of little use in mold treatment.

 

 

Q: What may be the other likely causes of mold exposure for adults apart from damp houses?

A: Food or water damaged buildings are the most common causes of mold exposure. Food is unlikely source in USA and EU where food testing is required for foods commonly mold contaminated.

 

 

Q: I was told that you should not use bleach because it causes the mold spores to open up and release the mycotoxins and that hydrogen peroxide is a better option. Can you comment on this? 

A: Chlorine bleach can help eliminate mold on hard non-porous surfaces like sinks, bathtubs, tiles, or glass. This is because the roots of the mold do not penetrate through this surface and so it is easily wiped off.

However, when mold grows on a porous material like wood or drywall, it spreads its roots deep into the material to reach more nutrients. So when you apply bleach to such a surface, you are merely changing the mold’s color on the surface. Bleach quickly dries off on the surface and will not reach into the deeper part of the material to the mold’s root. So, in a few days or weeks, the mold regains its color and grows back to become even worse than it was before you applied the bleach.

I would suspect that hydrogen peroxide would also be ineffective on these porous materials which is why replacement of these materials is the most effective treatment.

 

 

Q: Recently, it was suggested that we could use effective microorganisms (EM) to kill mold on the walls. Using good bugs to kill bad bugs. What are your thoughts on this?

A: I don’t know. Never saw articles on such treatment.

 

 

Q: If there is only an elevation of tartaric acid in the Organic Acids Test, can we be confident that the patient is definitely affected by Aspergillus?

A: Several pharmaceuticals contain tartaric acid salts in their drugs so you need a complete drug history before you can conclude that Aspergillus is the cause of high tartaric acid.

 

 

Q: If you are only treating the GI tract, why not use amphotericin, which isn't absorbed?   I use itraconazole nasal spray as I find colonization is usually cured by treating sinuses. 

A: Amphotericin B is comparable to itraconazole for several molds and may be preferable since it is not absorbed from the GI tract so will not cause liver toxicity. However, amphotericin B may be liver toxic when administered intravenously rather than given orally. I know one physician who lost his medical license because of his use of amphotericin given orally. His medical board did not appreciate the difference in toxicity between oral and IV administration.

 

 

Q: Shoemake and Heyman have indicated that the mold smell had a higher correlation to the bacteria actinomycetes than mold. Could that explain inconsistencies at times?  Have you seen WDB with actinomycetes and have you treated it any differently than you would mold, i.e. antibiotics, and which one?

A: I would not use smell to determine mold contamination. The best way is to use a professional mold inspector who uses laboratory testing.



Lindsay Goddard, RD

Food to Treat: Using the IgG to Help Your Patients | Speaker Panel

Q: Is a dried blood spot (fingerstick) sample as accurate as a blood draw?

A: Yes. The accuracy is the same. The option is given to accommodate patients who blood draws are more complicated.

 

Q: In your clinical experience, do people who have candida or aspergillus overgrowth react badly to saccharomyces boulardii?

A: That has not been my overall clinical experience. There have been patients that have reacted poorly to it, but not the majority. Since it is not consistent, it is one of the benefits to running the test, to understand how an individual might respond based on their own individual immune response.


Q: Is there any way to get the OAT and /or MycoTOX Profile covered by insurance?

A: The OAT can sometimes be covered by Medicare or TRICARE (military), but the MycoTOX Profile is rarely covered.

 

Q: Is it of benefit to also check peptide level reactions to food in addition to whole blood protein?

A: Testing the peptide levels makes a case by eluding that they are measuring individual parts of the protein versus the whole protein. However, they are still measuring IgG4 and IgA, which do not induce complement, and therefore not inflammation.. I was not able to find any studies showing the efficacy of this method in the literature. If you find any independent studies on this methodology, I would be very interested to see them.  

 

Q: Can you see certain trends in OAT markers for Long Covid patients?

A: Not specifically. Quinolinic acid is often elevated in the beginning, and/or recently post infection or vaccines. There are times the mitochondria are also stressed.  



Shanhong Lu, Md

Glyphosate and GBH as an EDC, a Slow, Multisystem Corruptor to Hormone Optimization and How to Become Glyphosate Resilient

Q: Thank you for your mineral connection (i.e. mercury and iodine). You mentioned Hyper Zinc. What should I be thinking with high zinc if there is no obvious source? Or high ferritin, if there is no obvious HFE or fatty liver?

A: A complete mineral profile will be extremely important and also GPL-TOX Profile and Glyphosate Test will also help to determine where the excessive zinc comes from as many pesticides use zinc as a carrier. 

Q: Can glyphosate pass to cow's milk which is sold to humans?

A: Yes

 

Q: If we see neuroinflammatory symptoms when we give patients glutamine, should that excessive glyphosate exposure be on the differential diagnosis?

A: Absolutely – I have tested so many people with autoimmune, cancers, ALS MS PD and endocrine disruption and elevated SHBG. Glyphosate is always present.

 

Q: When should we suspect a glyphosate problem and do a glyphosate test?

A: I recommend getting that test done right away along with a mineral heavy metal profile and genomic test. Do an environmental workup, if supplements do not work.

 

Q: In your experience, when you removed glyphosate load from the Parkinson's/ dementia patients, do their symptoms reduce substantially?

A: With immune – depolarization, removing glyphosate as soon as possible absolutely improve symptoms. One patient with PD over 10 years on triple drugs improved walking down stairs and started riding horses and hiking. Neuroinflammation in the brain is definitely a result of M1 M2 polarization.

 

Q: How do you determine Individual Tolerant Level?

A: I look at genetic (such as methylation, PON1, COMT, SOD, Dopamine receptors, Vitamin D receptor IL6 TNFa) plus their hormonal age (adrenal sex thyroid and pituitary) people with traumatic brain injuries are more sensitive also.

Q: Do you recommend intermittent fasting as a way to trigger autophagy and a means to help the body become more resilient?

A: I no longer recommend fasting because it causes more stress. Many women are genetically in-between-meal eaters, compliance is low, and the pituitary is not working well when fasting.

 

Q: What do you do for patients that are deficient in glutathione synthetase?

A: I use systemic detox binders (cleardrrops www.zoiglobal.com/drlumd and practitioners with a license can apply professional detox pro), Ca-D-glucarte 2000 mg a day and skip the conjugation relying glutathione pathway, which is not strong for BPA metals and so on.

 

Q: Could you explain once more how to increase/support phase 1 detoxification of the liver?

A: Metals and glyphosate both block phase 1 cytochrome P450 and drugs too. Decreasing exposure and systemic detox support is the key. Genetic studies on cytochrome P450 and PON1 are important.

Q: Is there a way that you can perform the OligoScan on somebody that is not in your presence? (e.g. via some sample of skin or something?)

A: Unfortunately no. A pathologist is needed for biopsies and I recommend going to www.theoligoscan.com to find providers. Feel free to text me at 530-925-0565.

Q: It seemed that you were saying in your presentation that PON1 acts on phase 1 intermediates. Did I hear that correctly, and if so, is PON1 considered a phase 2 enzyme? 

A: For water soluble pesticides (organophosphates ) PON1 is much needed to render the intermediate substrate nontoxic – still phase 1 process. 

Q: Which nutrigenomic software do you use?

A: I use puregenomic from pure encapsulation the most and I also use gxsciences.com.

Q: Since you listed X39 and AEON in association with stress control and other products that balance the branches of the ANS, does that mean you find that they help to balance the ANS? I use them but had not known of a mechanism that would affect the ANS aside from reducing oxidative stress.

A: X39 has been studied to balance blood flows in various regions and enhancing GABA Dopamine and Otropin has been tested by MAX pulse machine using HRV.   We have found over 90% people with significant improvement of SNS vs PSNS balance-parasympathetic improvement with 3 minutes after 4 sprays of Otropin.

Q: What do you use as an immune modulator?

A: I use ultimate immune (containing a patented formula muramyl peptide beta glucan and Glucarate). Please email me drlu@drlumd.com and we can open an account for you.



Elena Villanueva, DC

Managing the Complex Patient: Using the GPL-TOX and OAT in Clinical Practice | Mycotoxins: Considerations, Case Studies and Protocols

Q: What are the top three mind therapies that you have found to be most effective for healing? 

A:  It really depends on what is going on with the individual as to which tools and modalities will be the most effective. If we are looking at how to down regulate the SNS using mind-based therapies, tools like QTT (quantum time therapy), perceptual positions exercises, resonance repatterning, hypnosis, hypnobreath therapy, and meditation exercises can be super beneficial.  

If a client has dis-ease that is rooted in unresolved trauma or unprocessed emotions, incorporating a sequence of a combination of both mind and body therapies is how I see the best outcomes. For example, first teaching the client awareness of how their thoughts, emotions, trauma can effect their physiology and mental health. Then teaching them to master their own down regulation of their SNS and how to activate their PNS using tools like breath therapy, yoga breath therapy, EFT tapping, bilateral touch, and watching their stress metrics improve as they master their own 'circuit board'. Then moving into teaching them awareness around their conscious and unconscious mind, their thoughts, and what tools are available to address and resolve their unprocessed emotions and unresolved trauma using tools like somatic experiencing, QTT, parts integration, P positions, language, light, color, sound therapy, etc.

Q: What are the top three spiritual therapies that you have found to be most effective for healing? 

A: Teaching awareness of who we are as humans has been very powerful with my clients. 'Who we are' being a mind, body, and a spirit with both a conscious and an unconscious mind. And teaching our clients how to integrate their 'parts' so they can speak and live their authentic truth without shame, fear, anger, etc.

Helping them become aware also that they are living a human experience and that all they experience is happening for them, not 'to' them; that THEY are the ones creating their realities through their thoughts, stories, beliefs, and actions. The power for them to heal comes from within them more so than anything outside of them.  

I wouldn't say that we teach spiritual therapies, but rather we teach awareness of the power they have within ourselves to master our own minds, and ultimately our own realities. We focus on empowerment and awareness of their sovereignty. 

Q: How long do your patients/clients typically stay on maintenance? How often do they return for visits? 

A: Once our clients are back to 'baseline' with their health, we start teaching them about longevity and anti-aging and how to biohack for higher performance without compromising their long-term health. We encourage them to do their full functional blood labs, and hormones annually and we encourage them to do their toxins labs every other year to ensure they are not unknowingly building up and re-exposing themselves to toxins. They typically see us 2 to 3 times per year for their wellness programs with us. 



Learn new ways to help patients with difficult-to-diagnose and chronic health issues.

The tests discussed throughout each workshop are all used to help identify exposure sources and biochemical imbalances in individuals with chronic health conditions. The Organic Acids Test (OAT) contains multiple markers which may be influenced by environmental and mold toxins. Often, the combination of the OAT, MycoTOX Profile, and GPL-TOX Profile can be used to help identify how a patient might be getting exposed, as well as assist with correlating their symptoms back to these sources. Determining the underlying causes of chronic illnesses for patients is the key to integrative medicine, not just treating the symptoms. The Great Plains Laboratory continues to find new ways to detect these causes of many illnesses and study the correlations between the results and conditions.

Registration includes:

  1. 60-day access to the full conference recordings.

  2. Permanent PDF access to each speaker’s slides.

  3. The option to purchase continuing education credits (5 credits per day), whether you attend in-person, watch Live Online, or watch the conference recordings at a later date! See detailed information about credits.

  4. An interactive Workshop Hub website where you can live chat and network with attendees and ask questions to the speakers.

  5. And last, but most certainly not least, qualified practitioners will receive a free OAT.

Mycotoxin Properties and Metabolism: Part 2

This blog is a continuation of Mycotoxin Properties Part 1. Here, we discuss the less common, but arguably some of the more toxic mycotoxins that may come up on the MycoTOX Profile (Mold Exposure).


As a mycotoxin classified under the Aspergillus category, Gliotoxin has an average elevation range for people who are suspicious of mycotoxins between 200-2000 ng/g of creatinine. More extreme cases have been shown to be in the 20,000-25,000 ng/g of creatinine range. Although Aspergillus (particularly the fumigatus species) and Penicillium have been shown to produce Gliotoxin, some yeast can as well, particularly Candida (1). A study that looked at A. fumigatus strains from silos contaminated with mold found only 11% of the cultures to be gliotoxin producers (2). On the other hand, a study performed at MD Anderson Cancer Center, found 93% of A. fumigatus strains from respiratory and tissue samples produced gliotoxin (3). Other studies that compared environmental versus clinical A. fumigatus producing gliotoxin, have not only found geographical variations, but overall as the evidence suggests, it is found more commonly as the result of internal colonization rather than contaminated environmental sources (4). Gliotoxin is also commonly found in the soil, but in that case, it is most commonly produced by Trichoderma virens to support competition among the other fungus and bacteria (4). 

Toxicology

Gliotoxin has been shown to inhibit phagocytosis by neutrophils and transcription factor NF-kB, causing immunosuppression, which can potentially further influence cytokine production and mast cell degranulation (5,6). Apoptosis in monocytes and dendritic cells has also been observed. Research has also demonstrated that gliotoxin can inhibit NADPH oxidase and Glutaredoxin enzymes, influencing the system’s ability to tolerate oxidative stress (7). Other studies on laboratory mammals have found that gliotoxin exposure causes a decrease in blood pressure, gastrointestinal hypermobility, and altered sleep patterns (8,9). It has also been identified as a potent antiviral, antibacterial, and anti-fungal agent (e.g. Rhizoctonia solani, Botrytis cinerea, Colletotrichum spp., Pythium ultimum, Fusarium spp (10). 

Properties

Gliotoxin is a compound from the epipolythiodioxypipeazines family, which includes an internal disulfide bridge. It is this disulfide bridge that allows the cross-linkage with cysteine residues, which produces reactive oxygen species (11). It can be produced by A. fumigatus near the temperature of the human body at around 37 degrees Celsius (98.6 degrees Fahrenheit), which is unique for mycotoxin production (12). Gliotoxin has a melting point between 200 °C and 202 °C (392-396 °F) and has a solubility of 0.5-5 mg/L depending on the solvent, where organic solvents increase the solubility (13). Stability increases in acidic, dry environments, but Gliotoxin is extremely unstable and degrades quickly in alkaline and neutral environments with high moisture. There is little literature regarding the half-life of gliotoxin, however, a soil study found the half-life is highly variable and dependent on pH and moisture. In acidic conditions (pH 4), gliotoxin was stable for >30 days, but in alkaline water (pH 7.5), only 35% was stable on the 10th day of measurement. However, when in dry soil versus moisture-rich soil, regardless of pH, gliotoxin was completely degraded on the 10th day (10). 

Metabolism

There is limited data on the pathways utilized by gliotoxin in the human system. However, we do know that it can enter the cytoplasm of the cell, which can arrest the cell cycle possibly by interfering with DNA (9). Its oxidized disulfide structural form allows for glutathione conjugation which reduces it to the dithiol form. This is how it is taken up into the cell and increases its accumulation (9, 14). This reduced form is how it is generally found in the cells, and there is a maximum concentration allowance dictated by cell density. When glutathione levels decrease, the oxidative intracellular toxin creates an increased outflow from the cells, allowing for minimal amounts to have more of an impact (14). As it moves through the system, through the kidneys for elimination, it has been documented to be highly cytotoxic to renal epithelial cells at lower concentrations (9). 

Similar in structure to aflatoxins, particularly B1 (15), Sterigmatocystin (ST) is most commonly produced by Penicillium and Aspergillus (mainly A. Versicolor and A. nidulans), but can also be produced by FusariumBipolarisand even Stachybotrys and Chaetomium (16, 17). It is not currently monitored in food due to the lack of occurrence. Stored cheese and grains are the only documented contaminated circumstances and there have been no outbreaks associated with ST reported to date (16). It is mostly associated with being a potent liver carcinogen (18). The data was limited on ST, and information was difficult to obtain. 

Toxicology

ST has been found to be highly carcinogenic because it can easily react with DNA and be highly mutagenic. However, this only applies to the exo-epoxide formed post conjugation through phase II detoxification. The endo-epoxide has been shown to be less reactive (18). This is one reason it is said to be less toxic than Aflatoxin B1. It has been documented in mice to be hepatotoxic, with chronic and consistent exposures, and with mutagenic actions (16). Also known to increase production of reactive oxygen species, with enhanced lipid peroxidation (16). 

Properties

ST contains a dihydrofurofuran core, with a xanthone nucleus, and an attached bisfurn structure (16,18). It is insoluble in water, with a half-life in plasma of 46.5 to 55.8 hours and a melting point of 246 °C (474 °F) (19).

Metabolism

ST goes through cytochrome P450 oxygenase systems, which produces endo and exo-isomers. They are incredibly unstable, and so they are difficult to isolate from biological systems, hence measuring the toxin itself is likely more efficient than measuring the metabolites generated from metabolism (18). Human studies are limited. However, rodent studies have found the greatest tissue distribution resided within the gastrointestinal tract tissue with 100% elimination in 96 hours, 80% excreted in the first 24 hours in urine (19). Although, when tissue accumulation was compared to blood levels, they remained significantly higher in the tissue, though still with decreasing levels by a factor of 8 over 96 hours. This makes sense because ST also goes through enterohepatic recirculation via the bile, which is likely why tissue amount is extended over serum and urine (19). 

Both Roridin E and Verrucarin A mycotoxins categorized under the Stachybotrys mold, are relatively similar, though differences will be discussed as they arise. Roridin E is produced by Fusarium, Myrothecium, Trichothecium, Stachybotrys, and less commonly, the Betula cordifolia (the mountain paper birch tree) and the Podostroma cornu-damae mushroom (20, 21). Verrucarin A is also produced by Fusarium, Myrothecium, Trichoderma, and Stachybotrys, but differs in that Trichothecium, Cephalosporium, and Verticimonosporium can also produce it. Though not as common to come up positive on the testing, these are some of the more toxic mycotoxins measured. When exposed to trichothecenes the effects can be quite toxic. For Roridin E; irritation of the skin, mucosal layers of the intestines, and the nasal passage have been observed, sometimes leading to blisters and bleeding.  Ocular symptoms have been described as burning, blurred vision, conjunctivitis, and pain. Hypotension, nausea, vomiting, and potentially shock have also been documented (22).  Symptoms can be variable for Verrucarin A, but can be extreme and have cascading effects. The symptoms include bone marrow damage, nervous disorders, cardiovascular alterations, hemostatic derangements, immunodepression, gastric inflammation and lesions, anorexia, and dermatological lesions potentially leading to necrosis (23,24).

Toxicology

Trichothecenes are different than other mycotoxins in that they do not require metabolic activation, rather they react with biological systems, directly. Exposure can be through oral, dermal, inhalation, and parenteral routes, and once absorbed, they are able to move across the plasma membrane freely (22,23). Roridin has been shown to inhibit receptor tyrosine kinase, impact glucose-6-ph,osphatase in liver tissue, and also deplete glutathione (20, 25). One of the major components of Verrucarin A’s toxicity is their ability to bind to ribosomes, particularly at the 3’ end of large 28S ribosomal RNA. This inhibits initiation, elongation, or termination steps, therefore influencing protein synthesis and polyribosomal disaggregation (23). These mycotoxins can alter membrane structure, influencing the mitochondria, and have also been noted to inhibit RNA and DNA synthesis along with mitosis. Verrucarin A is known as a potent antibacterial and antifungal (23). 

Properties

Trichothecenes, including these two mycotoxins, contain a distinct 9,10 double bond, and a 12,13 epoxide ring, with an additional hydroxyl or acetyl groups at certain positions (20, 22,23, 26). They are lipophilic in nature but have a relatively short half-life. It is estimated that trichothecenes, in general, have a half-life of minutes to hours (27, 28). Both have low water solubility, with Roridin E at 0.01 g/L and Verrucarin A at 0.043 g/L (22, 23). There is no data on melting points for either one of these toxins.       
                                                                                                                                                                                                                                                                

Metabolism

Once absorbed into the system, they are metabolized in the liver by cytochrome P-450 enzymes and trichothecene-specific carboxylesterases. Through phase II detoxification, the major pathway utilized is glucuronidation and deepoxidation (22,23, 27). They are mainly excreted through urine and feces, but additional data beyond these pathways was difficult to find. One study that was done on a similar trichothecene produced by S. Chartarum, Satratoxin G, found that it was detectable in the blood of the mice being exposed intranasally from 5-60 min after exposure (26). Noting that the clearance from plasma was rapid and single compartment kinetics was observed. The highest concentrations were found in the nasal passage (480 ng/g), then the kidneys (280 ng/g), lungs (250 ng/g), and spleen (200 ng/g) had the next elevated amounts. Interestingly, the liver did not have as high of a concentration (140ng/g). The half-lives were variable in the tissues as well, with 7.6-10.1 h in the nasal passage and the thymus, and 2.3-4.4 hours in the other organs. When the urine and feces were evaluated, the cumulative excretion over 5 days was 0.3% of the total dose administered. The two mycotoxins were difficult to compare but do give some insight into the biochemical pathways of these toxins (26). 

Ennaitin B comes from the fusarium species, and though it is common in foods due to its resistance to food processing techniques, and being unregulated, it has also been found in water damaged buildings (29). It has been shown to be more toxic than Ennaitin A, and just as common in our environment (29). Research has shown it acts as an antibacterial (particularly to certain species of Escherichia, Enterococcus, Salmonella, Shigella, Listeria, Yersinia, Clostridium, Psuedomona, and Staphylococcus), and antifungal (Beauveria and Trichoderma) (29, 30).  

Toxicology

ENN B is most commonly known to inhibit acyl-CoA and cholesterol acyl transferase activity, which will inherently influence lipidemic levels, particularly with decreased free fatty acid availability and triglyceride biosynthesis (29). EEN B has also been shown to affect the mitochondria directly by influencing potassium uptake and decreasing calcium retention capacity of the matrix. This can cause the mitochondrial membrane potential to collapse. Cell cycle disruption, and apoptotic death, have also been observed with the presence of ENN B (31). Adrenal endocrine influences via reducing progesterone, testosterone, and cortisol have been noted even in smaller amounts (29, 32). Higher concentrations (10 µM) were noted to reduce testosterone and estradiol (33). It has been shown to be a potent cytotoxin in several human and animal cell lines, even at very low levels. This is amplified when other mycotoxins are present (29). 

Properties

ENN B is a cyclohexadepsipeptides that is composed of mostly valine, isoleucine, and leucine residues, and three hydroxy acids, usually hydroxyisovaleric (29, 31, 34). It is lipophilic in nature, giving it the ability to incorporate into the phospholipid bilayers of the cell membrane. They are ionophores, which allows them to have a lot of other variabilities in their activity (29). This leads to its ability to influence the selectivity of the pores and disrupt cation levels. Also, it has the ability to form complexes with alkali metal ions, with selectivity in the following order: K+ > Ca2+ ≥ Na+ > Mg2+ > Li+. Solubility is 0.018 g/L in water (31). With regards to half-lives, a study that evaluated the degradation rate within a human gastrointestinal tract model found a degradation rate of 79 ± 5% within the GI tract, with even more degradation of enniatin B in the colon after 24 hours (35). The melting point is 229°C (444 °F), which is the main contributing factor as to why it is not affected by food processing (31).  

Metabolism

ENN B enters the system via oral, dermal, or inhalation route. From the aforementioned study on the GI model and ENNs behavior, they found metabolites from ENN were adsorbed within the GI tract (more than the parent compound) and observed moderate blood-brain-barrier crossing (35). It has been noted to bioaccumulate in the lipid tissue in rats and disseminate throughout the tissue in chickens (29). It utilizes the P450 enzyme CYP3A4, which to note, is one of the main enzymes that metabolizes numerous drugs, and other contaminants (31,36). 

Chaetoglobosin A is one of the most toxic mycotoxins on the test with even small amounts being deadly. It is very common in water damaged buildings, and in fact, one study that looked at the prevalence found that out of 794 water- damaged building material, 49% had isolated Chaetomium species (37). Chaetoglobosin A is one of the major mycotoxins produced by the Chaetomium species (mainly Chaetomium globosum) and some Penicillium species (38, 39). There are 18 natural chaetoglobosin mycotoxins that have been identified and have been known to be an antimicrobial agent with some neocicidal and antifungal influences (40, 41). Unfortunately, the literature is sparse on this mycotoxin, and details regarding properties and metabolism were limited. 

Toxicology

Chaetoglobosin A has been shown to influence cell division by inhibiting cell movement, cytoplasmic division, and multinucleation (40). It has also been found to be a P450 inhibitor and influence apoptosis (40, 42). Research has shown it to be quite toxic to mammals. In rats, exposure by injection caused necrosis of the thymus and spleen, and degeneration of the spermatocytes (40). Evidence also suggests it to be cytotoxic, particularly in cancer cells, and influences the cytoskeleton, accompanied with apoptosis (40 and 41). There is evidence of it being teratogenic in mice fetuses, with documented skeletal malformations, micromelia of the forelimbs, fused ribs, and death (43).

Properties

Chaetoglobosin A is a member of the cytochalasan-type (48).  All 8 types have a similar 13-member macrocycle and perhydroisoindole skeleton, with an indolymethyl substituent on C-3, but vary in oxidation level, C-11 and C-12 methyl substituents additions (40). They have a melting point of 165°C-170°C (329°F - 338°F), but no data was available on solubility or half-life at this time (40).

Metabolism

The data is very limited on the metabolic pathways of Chaetoglobosin A in the animal system, with in vitro studies very much lacking in the literature. A dated study in 1978 found higher toxicity load through parental exposure versus oral dosing in rats and mice, alluding to low oral absorption (44). In this study, when the rats were injected with this mycotoxin, death was observed 10 minutes to 2 hours post-administration, with visceral congestion noted on autopsy (44). At lower injection doses, 36% mortality rate was observed in 6-48 hours accompanied by necrosis throughout the spleen, decreased thymocytes, spermatocyte degeneration, and pulmonary congestion. The other 64% that recovered, after 3 days, the only effects were on the thymus and testes, with no histological abnormalities after 7 days (44). In another study where the rats and mice were fed an oral diet contaminated with a 50% concentration of Chaetoglobosin A for 10-15 days, decreased weight was observed (38). 

This concludes the evaluation of each mycotoxin on the MycoTOX Profile. Hopefully, it helps in the understanding of these mycotoxins in nature, and potentially in our bodies. 

 

  1. Shah DT, Larsen B. Clinical isolates of yeast produce a gliotoxin-like substance. Mycopathologia. 1991 Dec;116(3):203-8. doi: 10.1007/BF00436836. PMID: 1724551.
  2. Dos Santos VM, Dorner JW, Carreira F. Isolation and toxigenicity of Aspergillus fumigatus from moldy silage. Mycopathologia. 2003;156:133–138. 
  3. Lewis RE, Wiederhold NP, Lionakis MS, Prince RA, Kontoyiannis DP. Frequency and species distribution of gliotoxin-producing Aspergillus isolates recovered from patients at a tertiary-care cancer center. J Clin Microbiol. 2005;43:6120–6122.
  4. Kwon-Chung KJ, Sugui JA. What do we know about the role of gliotoxin in the pathobiology of Aspergillus fumigatus?. Med Mycol. 2009;47 Suppl 1(Suppl 1):S97-S103. doi:10.1080/13693780802056012
  5. Pahl HL, Krauss B, Schulze-Osthoff K, et al. The immunosuppressive fungal metabolite gliotoxin specifically inhibits transcription factor NF-kappaB. J Exp Med. 1996;183:1829–1840.
  6. Niide O, Suzuki Y, Yoshimaru T, Inoue T, Takayama T, Ra C. Fungal metabolite gliotoxin blocks mast cell activation by a calcium- and superoxide-dependent mechanism: implications for immunosuppressive activities. Clin Immunol. 2006;118:108–116.
  7. Dolan SK, O'Keeffe G, Jones GW, Doyle S. Resistance is not futile: gliotoxin biosynthesis, functionality and utility. Trends Microbiol. 2015 Jul;23(7):419-28. doi: 10.1016/j.tim.2015.02.005. Epub 2015 Mar 10. PMID: 25766143.
  8. National Center for Biotechnology Information (2022). PubChem Compound Summary for CID 6223, Gliotoxin. Retrieved March 31, 2022 from https://pubchem.ncbi.nlm.nih.gov/compound/Gliotoxin.
  9. Gayathri, L., Akbarsha, M. & Ruckmani, K. In vitro study on aspects of molecular mechanisms underlying invasive aspergillosis caused by gliotoxin and fumagillin, alone and in combination. Sci Rep 10, 14473 (2020). https://doi.org/10.1038/s41598-020-71367-2
  10. Jayalakshmi, R., Oviya, R., Premalatha, K. et al. Production, stability and degradation of Trichoderma gliotoxin in growth medium, irrigation water and agricultural soil. Sci Rep 11, 16536 (2021). https://doi.org/10.1038/s41598-021-95907-6
  11. Waring P, Beaver J. Gliotoxin and related epipolythiodioxopiperazines. Gen Pharmacol. 1996;27:1311–1316.
  12. Kamei K, Watanabe A. Aspergillus mycotoxins and their effect on the host. Med Mycol. 2005 May;43 Suppl 1:S95-9. doi: 10.1080/13693780500051547. PMID: 16110799.
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  36. Ivanova L, Denisov IG, Grinkova YV, Sligar SG, Fæste CK. Biotransformation of the Mycotoxin Enniatin B1 by CYP P450 3A4 and Potential for Drug-Drug Interactions. Metabolites. 2019;9(8):158. Published 2019 Jul 27. doi:10.3390/metabo9080158
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  44. Ohtsubo K, Saito M, Sekita S, Yoshihira K, Natori S. Acute toxic effects of chaetoglobosin A, a new cytochalasan compound produced by Chaetomium globosum, on mice and rats. Jpn J Exp Med. 1978 Apr;48(2):105-10. PMID: 713122.
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  46. Walkow J, Sullivan G, Maness D, Yakatan GJ. Sex and Age Differences in the Distribution of 14C-Sterigmatocystin in Immature and Mature Rats. 1985. Journal of the American College of Toxicology.4(1). https://journals.sagepub.com/doi/pdf/10.3109/10915818509014504


LINDSAY GODDARD, RDN, LD/N

Lindsay Goddard is a Registered and Licensed Dietitian (RDN, LD/N), with a Masters in Nutrition, and a Bachelor's in Biology with a concentration in Human Physiology and Ecology. Her background allows for a comprehensive understanding of the connections and interactions between the body, the environment, and nutrition. Her experience consulting in functional medicine practices and hospital settings (Tampa General Hospital, University of Arkansas for Medical Sciences), has enabled her to take the biochemical information and apply it clinically, while bridging the gap between conventional and functional perspectives. She is excited to be a part of the GPL team, and hopes to support your mission in greater knowledge.

Workshop Q+A: Mold and Toxins: Integrative Strategies & Protocols

On March 25-27, 2022, GPL Academy hosted the Mold and Toxins: Integrative Strategies & Protocols live-streamed online. This three-day event focused on the epidemics of toxin exposure, including both toxic chemicals in our environment and mycotoxins from mold. These toxins can cause symptoms of many acute and chronic health disorders. Those who attended the summit learned how to use effective diagnostic and treatment protocols for their patients with toxin exposure and get them on the road to recovery.

The following Q+A is a grouping of responses from the workshop presentations. Click each presentation title to expand the answers from each speaker.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


Day 1 Q+A: Organic Acids

Click each presentation title to expand the answers from each speaker.

Introduction to the Organic Acids Test | Kurt Woeller, DO

Q: Rhizopus is used for tempeh, but Aspergillus is used to make miso and soy sauce. Just curious if furan-2,5-dicarboxylic acid might also be in those foods & thus be high in the OAT test?
A: Good question, but I do not know specifically.




Q: When we first use the OAT is there someone at the lab that will help us with understanding/interpreting it?
A: Yes. Great Plains Laboratory has lab advisors available.




Q: If arabinose is "elevated 80% of the time" and the reference range is +/- 2 standard deviations, why isn't the reference range higher? Or is it that of the types of patient’s functional medicine clinicians see, 80% have high arabinose?
A: The 80% is my impression. Something I have seen over the years in my practice. It is an approximate percentage.




Q: I often do OAT and NutrEval by Genova. When I compare nutritional markers, OAT rarely finds abnormalities in nutrients, but NutrEval very often finds abnormalities in nutrients status. Please offer an explanation.
A: I would recommend speaking to one of the biochemists at the Great Plains Laboratory about this observation. They might be able to provide more insights from a laboratory standpoint.




Q: I hear mixed things about fungal link to oxalates. Why is there such a wide discrepancy in opinions on this?
A: There is a wide discrepancy about a lot of things in medicine, science, and nutrition. From my experience and research (and I know Dr. Shaw’s too from Great Plains Laboratory) there is a strong correlation.




Q: Will the nutrients that are low (CoQ10, B2, b12, etc.) get better when you treat the mold/candida/etc.?
A: Sometimes.




Q: Should we give them those nutrients while fixing the underlying issue?
A: I like to in most circumstances.




Q: Or will they not absorb those nutrients because of the overgrowth?
A: They should still get absorbed.




Q: Is DOPA altered with Parkinson?
A: It can be.




Q: How come my sample test I got before showed Arabinose normal level is < 29 instead of <50? data-preserve-html-node="true" data-preserve-html-node="true"
A: The reference ranges changed based on age and sex. The sample I showed was just a sample from my practice.




Q: Do you know what may cause burning mouth syndrome in a patient? She has mild white coat of tongue; do you think this is candida or nutrient deficiency?
A: Very likely Candida. Research mineral deficiency linked to this condition too.




Q: If a client’s marker is between the first and second deviation but not necessarily “high”, do you still treat if client has symptoms? (Examples would be in the case of 4-cresol or arabinose being in between the first and second deviation.)
A: Yes. This is reasonable to do if you suspect there is a developing problem.




Q: Oxalates appear to be a sensitive, but very nonspecific test. What is the purpose then of testing it?
A: Some people are extremely sensitive to oxalates. Like any marker, it is always important to correlated to a patient condition.




Q: Emphasis is on elevated levels of different markers. What about negligible to low levels of different markers? Speaker addressed negligible levels of amino acids as being normal, what about other biomarkers. When should we be concerned?
A: For most things, low values have no known clinical significance. This changes though when looking at neurotransmitters. The amino acid metabolites are not the same things are directly assessing amino acids. When neurotransmitter metabolites are low that can be significant, as well as certainly nutrients such as Ascorbic Acid and Vitamin B6.




Q: What is the significance of very low metabolites in mitochondrial markers?
A: No known clinical significance according to Great Plains.




Q: Can you see mild elevations in fatty acid oxidation markers in people who are carriers for some of the inborn errors of metabolism in fatty acid metabolism?
A: This may be possible from my understanding.




Q: Is aspartame high from eating a meal the night before testing? Or is it only high if someone regularly eats aspartame?
A: It could be high ikf ingested the night before.




Q: If #28 marker is just slightly low, Aconitic - what does this indicate?
A: No known significance according to the lab.




Q: There are cases of asymptomatic positive stool test for C diff toxin. Do we need to treat it?
A: I would, at least with some probiotics.

Invasive Candida and Various Health Issues | Kurt Woeller, DO

Q: Is burning mouth syndrome candida?
A: Yes. It could be. Do some research on nutritional imbalances that could cause this too.




Q: Do edible mushrooms increase fungal levels in the body?
A: Not that I know of.




Q: Is Biocidin useful for Lyme dx?
A: There are many practitioners who have used Biocidin for Lyme. The company at BioBotanical Research would have more information on this.




Q: Do you use the biofilm busters for a time before starting the antimicrobial?
A: Typically, not with a new patient who is new to integration and functional medicine. I often rely on the botanicals first and then graduate to biofilm busters as needed.




Q: Any recommendations for fungal sinus infections?
A: Compounded nasal Amphotericin B or Itraconazole. Biocidin LSF can be used intranasally too. Contact BioBotanical Research as if they have additional information.




Q: What was the article that was recommended re invasive candida?
A: Candida Pathogenicity Mechanism - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654610/




Q: Can an elevated arabinose indicate conditions other than candida? Or is it specific?
A: It can be elevated from diet. So, it is critical people follow the instructions on the test collection form.




Q: You mentioned the connection between candida infection and the potential for leaky gut. I'm curious, are there any markers in the OAT test that may indicate that leaky gut could be an issue?
A: There is not a specific leaky gut marker. The Arabinose is about as close as a marker comes on the OAT for this condition.




Q: Could you deduce that a persistently high homocysteine on blood testing should prompt OAT testing looking for metals/chemicals?
A: I do the OAT for everyone that comes into my practice. However, regarding homocysteine/metals, etc. there are other tests to look for too such as environmental chemical exposure.




Q: You mentioned that organic acid markers for mold can be negative, but mycotoxin results can be high for past mold exposure. Why is this?
A: The mycotoxins are different chemicals from the organic acids. Therefore, the MycoTOX profile needs to be looked at as a separate test.




Q: Is there any evidence of Lyme in the OAT test?
A: Not specifically.




Q: Again, please explain the difference between the OAT mold markers and mycotoxin test. Which one is indicative of current mold exposure verses past exposure?
A: If an OAT mold marker is high that is active exposure (most likely) or at least lingering mold colonization (active) in the body from previous exposure. However, the organic acids linked to mold exposure as completely different chemicals from mycotoxins. It is possible to have a mycotoxin stored in the body for months even though someone is no longer being exposed to mold spores. It would also be possible to have mold colonization in the gut if the mold just continues to replicate itself without being treated. The bottom line is do not rely on the OAT to diagnose mycotoxin exposure.




Q: Can candida cause an elevated serum myeloperoxidase level?
A: Most likely if the level is serious enough and there is highly active neutrophil activity. I have not done this type of testing though.




Q: So, are you saying we should use manuka honey to break up biofilms? Or how was manuka honey relevant to candida?
A: I was only using those slides as a point of discussion about botanicals in general having anti-biofilm properties.




Q: Regarding Nystatin, can you please comment on Nystatin resistance and Botanicals for Aspergillus?
A: Nystatin will have some affect on Aspergillus, but Amphotericin B orally seems to work better. But there is literature out there indicating the liposomal Nystatin is a treatment option for Aspergillosis.




Q: If using Nystatin to treat candida will that help a suspected candida/fungal caused rhinitis?
A: Not likely, unless it was compounded into a nasal spray. At least this has been my experience with Nystatin orally is that it seems to have little effect on yeast outside the GI tract.




Q: If you have a patient that has candida issue and you have addressed the root cause as to why will the candida correct itself since root cause gone? or will the patient still have to be treated for candida?
A: Working on root cause is always the best overall approach to take. But they still may need to treatment to bring the levels down and make it easier for the microbiome to regain control.

Clostridia Bacteria Toxins and Various Health Issues | Kurt Woeller, DO

Q: Since Biocidin has echinacea in it, does not exclude patients with auto immune disorders from taking it?
A: I have never seen Biocidin at the dosages recommended by the company exacerbate an autoimmune problem.




Q: Can you touch on Clostridia spp on the OAT vs a stool test when the results do not match up?
A: The OAT markers are more specific to various clostridia bacteria. Stool testing for Clostridia difficile is specific for toxins A and B. These are often not present even in people dealing with bowel problems, but this test should be done if a serious C. diff. infection is suspected. However, the OAT overall is more sensitive to of clostridia bacteria infections.




Q: What about spore-based probiotics to deal with clostridia?
A: This can be helpful. I personally use a lot of Core-Biotic from Researched Nutritionals and Proflora 4R from BioBotanical Research.




Q: At which point is a stool test also indicated?
A: This can be done at any point, particularly if you want to assess digestive function overall or identify other pathogens. Consider a stool analysis to be complementary to the OAT and an often-necessary test on its own.




Q: Can the posting method be used with Biocidin and other herbals as well?
A: Yes. Pulsing could be done with other botanical supplements too, not just Biocidin.




Q: Why are some people so prone to having recurrent clostridia infection?
A: This likely has to do with many factors such as overall microbiome status, the presence of toxins such as chemicals and mold, and poor immune function.




Q: When you used Biocidin for 6 weeks, when was the binder used in relation to the dosing of Biocidin, and how many times was Biocidin used on daily basis? I dose Biocidin three times daily.
A: A binder can be used in between dosing of the botanical at least twice daily. Best to take away from other supplements by at least 90 minutes to 2 hours.




Q: When you believe a person has clostridial challenges, but the markers are normal, what would you use to begin excretion of clostridial?
A: You could use the same things discussed with regards to active clostridia such as the spore probiotics, e.g., CoreBiotic, as well as botanicals.

High Oxalate and Various Health Issues | Kurt Woeller, DO

Q: Rather than discourage a diet of healthy foods, wouldn't it be more ideal to focus on the reason for elevated oxalates like dysbiosis/leaky gut?
A: I never discourage a healthy diet, but for some people they do need to reduce high oxalate foods (even some of the healthy ones) for a while to get their levels down, and at the same time as addressing underlying gut problems and dysbiosis. There are plenty of healthy foods that are not high oxalate.




Q: Could high oxalates also lead to interstitial cystitis?
A: Yes, from my understanding high oxalates can be linked to this condition.




Q: Sally Norton talks about yeast as protective against dietary oxalates. Have you heard this?
A: I have, but I do not know the specifics.




Q: I'm curious if you consider Blastocystis hominis to be a problem always. Microbiome research is coming out now that it is associated with better metabolic health and discourage its eradication.
A: B. hominis is a problem for some people. However, I have seen it show up in random stool testing where the primary reason for the test was not anything specific to parasite analysis. https://pubmed.ncbi.nlm.nih.gov/33432175




Q: Patient with good response to a low oxalate diet but shows no oxalates or yeast on OAT. She still has body pain which increases noticeably when she eats more oxalates. Is it possible that she does not release oxalates well?
A: Yes. There can be stored oxalate that either are not be released or dissociated into soluble forms in body fluid.




Q: Should a person take vitamin K 1/2 with calcium/magnesium prior to oxalate meal?
A: Vitamin K has a complementary effect on calcium regulation by assisting in its storage into various body tissues.




Q: Can oxalate level be confirmed on 24-hour urine collection?
A: Yes.




Q: Can you expand on the lung CT scans, why were those ordered? Was that showing oxalates in the lungs? Was that patient having respiratory issues due to high oxalates. Simply curious about how/why that patient had a CT and didn’t know it would show up.
A: That was a paper looking at Aspergilloma infection and associated calcium oxalate crystallization. My recommendation is to look up the article and read it for more details.

Neurochemical Imbalances and Quinolinic Acid Toxicity | Kurt Woeller, DO

Q: Do keto diets increase LPS then?
A: From my understanding they can be associated with increased LPS.




Q: Is there another method to measure lithium levels other than hair analysis?
A: Blood levels are typically used for people on lithium medication. There may be a lab that does intracellular analysis of lithium.




Q: What would you think when someone responds badly (anxiety type symptoms) to 5 mg lithium orotate?
A: I have seen this too, but not very common. I would start looking at other mineral imbalances.




Q: Have you been seeing elevated quinolinic acid in patients with long covid? Or any other markers that may help explain common long covid symptoms? Thinking about the implications of neuroinflammation in this population.
A: Not yet, but I have not had a lot of long covid patients at this point.




Q: Do you see elevation of neurotransmitter markers in patients on SSRI or dopamine agonists or similar? Also is there a negative side to super dosing glutathione-2000mg plus?
A: Yes, this can happen. There is a negative feedback mechanism on glutathione production. High dose could also increase detoxification affects which a patient may not tolerate.




Q: Can you please clarify what you mean by resveratrol "decreasing microglia"? thanks.
A: It helps to decrease microglia activation. Therefore, Resveratrol can be helpful for brain inflammation and oxidative stress.




Q: L-cysteine can substitute for NAC as a useful precursor to glutathione, since I believe, NAC is converted to L-cysteine anyway? And if NAC is banned soon as a supplement, a substitute may be necessary in some cases.
A: Correct.

Additional Case Studies: Lab Reviews and Treatment Options | Kurt Woeller, DO

Q: Do you see die off reactions / Herx type reactions with Biocidin? Do you ever titrate up on it, or do you just start at full dose?
A: Depends on the sensitivity of the patient. Starting at a lower dose and titrating is certainly appropriate to do. Herx does not always happen, but more so in the sensitive patient. In my experience, it occurs about 30% of the time.




Q: How often are you using toxin/mycotoxin binders using only OAT tests showing positive yeast/clostridia markers?
A: Often. In general, I use binders about 80% of the time, but in some of the kids I treat it is difficult to do.




Q: I use soil based probiotic same as spore-based probiotics. Can you stay on spore-based probiotics for chronic use?
A: I do not like to use them for extended periods of time, but instead use them strategically as highly needed for certain patients. For example, 60 to 90 days for most clostridia problems.




Q: How long after a 14-day round of rifaximin would you recommend retesting (Dx: SIBO)
A: Two weeks




Q: Can you treat clostridia and a presumed yeast overgrowth at the same time? Put a patient on Biocidin and nystatin for example for a couple of months? Would doing a SIBO protocol help with both clostridia and yeast (using botanicals to treat SIBO)?
A: Yes, yes, and yes, most likely.




Q: I am not sure that I understand why you prefer daily dose of Biocidin for 3 mo. instead of daily for 3-6 weeks and then pulse as it seems that combination worked very well for you?
A: Depends on the patient and I have used multiple methods. The pulsing is generally used for recurrent issues. I have had some situations where I was daily dosing, check the MOAT at 6 weeks and the clostridia is still present. Then switch to a pulsing method, rechecked the markers and things had normalized. During my talk my goal was to show various options with the understanding that there is no single way that is going to work for all people.




Q: If succinic is high but your TOX test is not remarkable, mold not an issue and you still suspect a chemical, is there another chemical testing method/direction you have done?
A: This could be from Glyphosate too. I just came across this information in Stephanie Seneff’s book called Toxic Legacy. Can you discuss low Aconitic marker? According to GPL and the lab report it has no known clinical significance. I am looking into more as ongoing research.




Q: Do high thallium levels have any impact of concern?
A: Yes. Thallium has similar toxicities to Mercury. I see high Thallium in about 5 to 10% of hair metal tests that I do.




Q: Can you share some sources / reference for low cholesterol as risk factor for mental health doze?
A: There is so much information on the Great Plains Laboratory website. Go to their Resource section and look for past webinars and articles on this topic.




Q: At what level of cholesterol (for adults) would you consider low and decide to supplement?
A: Levels below 160 are considered not ideal. Mostly in my practice, when I look to supplement with Sonic Cholesterol, is levels around 120 to 130.




Q: Is presence of enterotoxigenic E coli going to show any abnormalities on OAT?
A: This would likely show up in the Bacterial Markers section.




Q: Do you recommend activated charcoal during the protocol?
A: It is okay but can be constipating. I prefer the GI Detox+ from BioBotanical Research.




Q: In your experience, is a low oxalate diet required for life or is that a temporary change when working through issues?
A: Some people will do it for life, particularly if they have struggled significantly with oxalates before. However, if the oxalate is mostly coming from fungal sources than a lifelong low oxalate diet is not necessary if the fungus is treated. Depends on the patient scenario, but typically it is not need lifelong for some people.




Q: Some patients with glutathione deficiency, are sensitive even to small dose of glutathione replacement. Are there markers that can indicate reaction to glutathione or is that just indicative of high toxicity? What do you recommend for them?
A: There are no markers that would indicate a tendency towards individual reactions. Every person is different with regards to their individual reactions. For many sensitive people, you have to dose things at a very low level. Start low and go slow is always a good method for sensitive patients.




Q: How long do you use the binder like GI Detox?
A: Typically for the duration of treatment of the candida, bacteria, and mycotoxins.


Day 2 Q+A: Hidden Threat of Mold and Mycotoxins – Testing and Treatment Protocols

Click each presentation title to expand the answers from each speaker.

Organic Acids and Mycotoxins: Correlations With Mold in Various Chronic Illnesses | William Shaw, PhD

Q: GPL recommends NOT using glutathione prior to testing however, I have seen that without glutathione many tests are negative, and the patients have a lot of s/s of mold toxicity.
A: To my knowledge, there is no published or unpublished study that this is true. Also, it goes against the scientific fact that glutathione reacts with mycotoxins to form large adducts that will be invisible to a mass spectrometer. Show me your before and after data (at least 10 cases) and I will publish it.



Q: Is Gliotoxin also an environmental mycotoxin or is it primarily thought to be due to candida?
A: Gliotoxin is due to both Candida and mold.



Q: I have a current client with high levels of Citrinin, and I'm curious whether this would primarily come from diet or due to a GI infection of an organism like Aspergillus?
A: High levels of mycotoxins in the USA are almost all due to water damaged buildings but the mold from such buildings often may colonize the lungs, sinuses, and GI tract.



Q: How do we tell whether mycotoxins are present in the environment and are showing up on a mycotoxin test or if they are present due to fungi in the gut? Am I correct in thinking that if the OAT shows fungal markers, the gut is to blame?
A: The presence of mold markers in the OAT test can indicate both the presence of mold in a water damaged building and the presence of mold in the GI tract.



Q: What makes the difference between responses between two people exposed to the same mold? can you be exposed and not be affected? is there a way to make yourself resistant to mold illness?
A: There are many genetic factors that influence response to mold infections and mycotoxins including many glutathione and cytochrome P450 factors.



Q: Clarify my Question: 'urinary mycotoxin testing vs. serum mycotoxin antibodies...'
A: Vodjani reported that there was a significant relationship between mold antibody levels and mycotoxin antibody levels, so mycotoxin antibodies are an indicator of mold allergy, not mycotoxin toxicity. Urine mycotoxins are the best indicator of non-allergic mold toxicity. There are hundreds of articles on urine mycotoxins and their clinical effects by a number of independent researchers but only a handful of articles on mycotoxin antibodies, all written by employees of the companies selling those tests.



Q: How do you get for sinus fungal colonization?
A: Mayo clinic published a study indicating that fungi are the main source of sinus infections which almost always are due to inhalation of mold spores in a water-damaged building.



Q: How did you clear the Zearalenone from your dog? did you use binders?
A: The dog went from near death to completely well after switching to a grain-free dog food in about one day. I did no other treatment. I had spent thousands of dollars on vet visits and lab tests that were zero benefit. Our vet continues to recommend dog food with grains. Contaminated dog food from moldy grains is probably the most common reason for vet visits for your dog. Completely ignore your vet’s bad advice on dog food.



Q: If someone only has one mold show up on their test, is it really that concerning? And do patients really have to give up the foods the molds are found in? Is that a strong source of mold for most people?
A: The most important factor is the amount of mycotoxins found, not the number of mycotoxins. Food is not a major source of mold in the USA. If the mycotoxin is double the upper limit of normal, I think the person has a significant problem.



Q: How long would a patient have to be off Mycophenolic drug in order to be tested?
A: The half-life of mycophenolic acid is 17 hours. In 5 half-lives (85 hours or 3.5 days), 97% would be eliminated. To be safe, it might be better to say 4 days off the drug.



Q: To help diagnose whether mycotoxins are causing or contributing to patient's illness, how helpful would it be for them to simply live somewhere else for a week or two? (Assuming they could find a mold-safe house)
A: Unfortunately, if the patient is colonized, they would be taking their mold with them to their new home. Testing is better than guesswork.



Q: How did you treat mold in your car?
A: The dealer (Hyundai) had a procedure. I don’t know how it was done, but it seemed to clear up the mold.



Q: Will you be covering anything on what antifungals to use when?
A: Itraconazole (Sporanox Brand Name) is effective against most molds and is reasonably priced. Voriconazole is thought to be more effective against more molds but is pricier. Nystatin and Diflucan are not nearly as effective.



Q: How long do you typically use binders to help mycotoxins? What would be the average time?
A: I would recommend one month. I do not think formal studies have been done.



Q: Do you recommend pulsing binders?
A: I see no benefit in pulsing.



Q: OAT mold metabolites are indicative of growth in GI exclusively?
A: I suspect that the markers are mainly of GI origin since the markers decreased following the use of nystatin which only kill yeast/fungi in the GI tract. The GI tract provides all the nutritional factors required by mold in abundance. I don’t think that would be true of sinuses or lungs.



Q: When someone goes on vacation or gets out of the house (or source of mold if it is at work or a school), will a lot of their symptoms get better? And how quickly?
A: Getting out of the moldy environment is always helpful but the colonized person is taking the GI mold with them wherever they go.



Q: What supplements / medicines should a patient take while mold remediation is being done? (I'm sure best is moving out but if cannot how to treat to avoid more future problems?)
A: If remediation is not done, the person will have to be treated again and again with antifungals and binders.



Q: So just to confirm, if you are positive on urine mycotoxin test, it means ACUTE exposure? How do you determine long-term exposure?
A: Long-term exposure is determined by clinical history of symptoms and knowledge of the mold in the home/office/school. For example, when did the flooding of the house first happen? When did the water pipes first develop a leak?



Q: Do you recommend treating with medicated nasal spray in cases of positive mycotoxins and upper respiratory symptoms?
A: I think that the standard treatment with antifungals and binders will clear up respiratory symptoms as well if systemic antifungals like Sporanox are used.



Q: So positive results on urine MycoTOX panel mean ACUTE exposure?
A: I would say that the presence of mycotoxins indicates current exposure which can be from moldy buildings and/or previous colonization.



Q: I have a male patient who keeps getting acute pancreatitis, for no reason; could this be mold?
A: Yes, there are a number of articles relating pancreatitis to mold and even pancreatic cancer. Aykut, B., Pushalkar, S., Chen, R. et al. The fungal mycobiome promotes pancreatic oncogenesis via activation of MBL. Nature 574, 264–267 (2019). https://doi.org/10.1038/s41586-019-1608-2 Firsova VG, Parshikov VV, Kukosh MV, Mukhin AS. Antibacterial and Antifungal Therapy for Patients with Acute Pancreatitis at High Risk of Pancreatogenic Sepsis (Review). Sovrem Tekhnologii Med. 2020;12(1):126-136. doi: 10.17691/stm2020.12.1.15. PMID: 34513046; PMCID: PMC8353699.



Q: Assuming you are not a dog, how contaminated are cereals, peanuts, coffee, etc with mold in the USA? Are legumes a significant source of mycotoxins?
A: In the United States, most foods are checked for mycotoxins. Any food may have mycotoxins.



Q: Do frequent rounds of antibiotics increase the risk of mold and mycotoxins to spread in the body?
A: I know of no studies but suspect the normal flora keeps molds in check.



Q: Do you think it is worth doing a MycoTOX test in patients who are in hospice with hepatocellular carcinoma? Is it too late to do anything at that point? I have so many patients with HCCA, one is a husband and wife:( thank you
A: Aflatoxins from mold-contaminated food and moldy buildings are a major cause of hepatocellular carcinoma. I could find no reports of diminishing the cancer once it has developed but it might be worth a try. If certain foods or building are suspect, mycotoxin results could be used to build a lawsuit case for the family of the couple.




Q: Would an isolated elevation of 14 in marker #6 on OAT, with high (98 oxalic) , and high HVA in a cancer patient, be concerning for aflatoxin or ochratoxin tox ? or maybe just a food exposure prior to testing? this is the conclusion of the staff.
A: Mold such as Aspergillus is common in cancer patients treated with chemotherapy. Many hospitals administer antifungals prophylactically with chemotherapy to prevent systemic fungal infections. High HVA may be due to certain tumors like neuroblastomas.



Q: What is a typical antifungal that is used, Diflucan or nystatin?
A: Not nearly as effective as itraconazole for mold. Voriconazole more effective and more expensive.



Q: Regarding the fibromyalgia patient treated for mold, that had reduction in mold furans in OAT, was she given Nystatin or a systemic anti-fungal?
A: I think both.



Q: When using binders for mold are there specific binders recommended for specific mold mycotoxins?
A: I would recommend GI detox for all since it has both clay and charcoal (NBNUS.com).



Q: Can you explain why some of the "oxalate" experts discount the mold connection to oxalate?
A: I suspect they have had minimal experience and access to OAT and Mycotoxin testing and the appropriate research papers.



Q: What are your thoughts on the GPL urinary excretion test vs ones that test antibodies? Wondering if more sedentary patients with depleted glutathione may not show as much mycotoxin exposure.
A: I suspect the opposite is true. When glutathione covalently bonds to mycotoxins, the altered mycotoxins are a much higher mass than cannot be detected by the mass spectrometer.



Q: How long was the Sporanox treatment regimen for the 3-year-old with Autism treated by Dr Baker thanks
A: The child recovered completely after 6 weeks of the antifungal, but the treatment was continued for a much longer time period. The child continued on Sporanox at lower doses for about 3 years.



Q: 3-year-old child that was switched to Sporanox from itraconazole, Were there less herkzheimer reactions on Sporanox?
A: The switch was made because the parent thought the Sporanox was more effective.



Q: I thought Sporonox is the brand name of itraconazole. Yet your slides make it sound like two different drugs (the 3-year-old with autism slide). Am I missing something?
A: Many physicians suspect that generic brands of drugs are of lower quality or less potent than brand names. The parent thought the child’s progress was better on the brand name Sporanox. The Sporanox brand of itraconazole has been developed and marketed by Janssen Pharmaceutica, a subsidiary of Johnson & Johnson. The three-layer structure of these blue capsules is complex because itraconazole is insoluble and is sensitive to pH. The complicated procedure not only requires a specialized machine to create it, but also the method used has manufacturing problems. So there may be real differences in the 2 products.



Q: Have you seen higher incidence of kidney stones in patients with high oxalate?
A: I have encountered several patients who developed kidney stones after starting diets with frequent spinach salads or spinach smoothies. Spinach is the food with the highest oxalate content.



Q: Is there a plan from the GPL Lab to expand the MycoTOX Profile to include other mycotoxins?
A: Yes.



Q: Can you discuss sinus colonization and how to test?
A: If there is sinus colonization, GI colonization will follow shortly as sinus leakage goes into the esophagus and GI tract. X-rays of the sinuses can be helpful to look for oxalate stalactites formed by colonizing molds. Mold cultures of the nose and urine mycotoxins also helpful.



Q: Do you need to do provocation (i.e. glutathione or EDTA) prior to doing the MycoTOX Profile?
A: No.



Q: Do you need mycotoxin testing and OAT to exclude most mold infections or is one test adequate as a screen?
A: The OAT only screens for Aspergillus and Fusarium so both are needed.



Q: Pulmonary aspergillosis (farmer's lung) treatments?
A: Remove from exposure, then treat with Sporanox. If severe, surgery may be needed.



Q: How does markers such as Melanocyte Stimulating Hormone, antidiuretic hormone or MMP-9 compared to the mycotoxin urine test?
A: None of these markers are specific for mold. These markers may sometimes be useful in patients with confirmed mold diagnosis



Q: If the OAT finds mold like aspergillus, is it assumed that the patient must be ill affected? or can you have mold in the OAT and have no issue or reason to treat?
A: I have recommended treatment in every case that the OAT mold markers were elevated.



Q: Can a mold toxicity situation produce a raised ferritin situation? I have a 50-year-old male with this situation (not hemochromatosis).
A: Many mycotoxins, especially aflatoxins, are harmful to liver. Ferritin is raised in liver toxicity.



Q: What is the best way to treat ochratoxin?
A: Ochratoxin is treated like all mycotoxins. Remediate moldy living spaces, treat with antifungals, then follow with one month of binders (GI detox, NBNUS.COM has both charcoal and clay).




Q: I see moderately high MPO on many labs but too high for heart disease and no apparent Infection? Can elevated MPO by from stealth gut infection be caused by fungus?
A: Mold fungus can indeed cause heart disease. Here is a resource.



Q: Why do mycotoxins often rise after starting treatment?
A: As molds are killed, they will release all mycotoxins that are stored intracellularly which are then absorbed and excreted into the urine.



Q: If patient can’t move or get away permanently from the exposure or remediation hasn’t quite been a success, can you perhaps pulse antifungals or herbal antimicrobials ongoing for long term?
A: You can do this, but you run the risk of drug resistance if you use this approach too long.



Q: If the mold is in hollow spaces like lung or sinuses does the antifungal treat that effectively?
A: Antifungals will treat any area of the body that has a blood supply. Lobectomy is commonly done when the infection of the lung is severe.



Q: If someone has known lung colonization, home tested positive, awaiting results, am I to assume this would be a patient who most likely would require stronger antifungal treatment, ie Sporanox and not as likely to respond to herbal therapies?
A: Yes.



Q: Can you speak to which probiotics specifically can help?
A: Lactobacillus plantarum and rhamnoses have been shown to degrade aflatoxins.



Q: Can carbon c60 be used as a binder?
A: Carbon 60 is a molecule made up of 60 carbon atoms. The layout of the atoms forms a molecule shaped like a soccer ball. Carbon 60 was first used in nanotechnology and electronics. Charcoal is very cheap and effective. Why not use charcoal?



Q: I know MMS is controversial, but I use it a lot with patients, and it is miraculous. Have you any thoughts on MMS and mold?
A: Miracle Mineral Solution is an oral liquid solution also known as "Miracle Mineral Supplement" or "MMS." The product, when used as directed, produces an industrial bleach that can cause serious harm to health. The product instructs consumers to mix the 28 percent sodium chlorite solution with an acid such as citrus juice. This mixture produces chlorine dioxide, a potent bleach used for stripping textiles and industrial water treatment. High oral doses of this bleach, such as those recommended in the labeling, can cause nausea, vomiting, diarrhea, and symptoms of severe dehydration. Since this substance is a powerful oxidizing agent, it is mutagenic and carcinogenic. I personally communicated with a woman who developed GI cancer after its use. Another parent had her child taken away by government child protective services after using it on her child. It undoubtedly is a potent antimicrobial but there are so many safer things, why take the risk?



Q: How long should someone be off Glutathione prior to testing?
A: Two days.



Q: I have a patient with moderately advanced Parkinson’s with moderate amounts of mold. When I put him on binders, regardless of the time of day, it decreases/binds his medical prescribed dopamine. As his L dopa is prescribed 4x/day. Other suggestions?
A: Use antifungals for a month before any binders. Then retest. If mold is gone, don’t use binders. If binders are used, use them 3 hours after L-DOPA.



Q: How would you explain increase in urinary mycotoxins after glutathione provocation compared to the urinary mycotoxin test done on the same individual without glutathione provocation prior?
A: To my knowledge, there is no published or unpublished study that this is true. Also, it goes against the scientific fact that glutathione reacts with mycotoxins to form large adducts that will be invisible to mass spectrometer.



Q: How do you time treatment of Mold in a patient with SIBO?
A: I would say exactly the same as a non-SIBO patient.



Q: Do molds have any impact on MS?
A: I have found mold involvement in virtually every neurological disease: MS, autism, ADD, Parkinson’s, Alzheimer’s, and ALS.



Q: I have three clients with mold exposure in the same household. Two out of three showed high levels of mycotoxins but the one that was immune compromised barely showed up on the MycoTOX Profile. Any reason why would one not excrete metabolites?
A: The big suspicion is that the person with the lowest mycotoxins spent less time in the moldiest parts of the house. That has been the reason in other cases I am familiar with. I doubt it is due to immune system compromise.

Mold and Alzheimer’s: An Unacknowledged Pandemic | Dale Bredesen, MD

Q: Amyloid plaque is misfolded fibrinogen from excess iron and low Vitamin C per Dr Robert Thompson. Does this fit into your management?
A: That is incorrect—amyloid plaque has many components, but the major proteinaceous component is the beta-amyloid peptide (of varying lengths, mostly 40 and 42 amino acids).



Q: Can you repeat what you said about low Triglycerides and low zinc? How does this link to Alzheimer’s?
A: This is simply an observation: many of the patients with type 3 (toxic) Alzheimer’s have low serum zinc and low triglycerides. Therefore, if you notice this in the setting of other features of type 3, it supports the diagnosis. We do not yet know the mechanism for these phenomena.



Q: How do you recommend testing for glutathione levels? Is whole blood via LabCorp sufficient?
A: Yes.



Q: In treating patients with cognitive decline and mycotoxin issues, do you find any contraindications in using ketosis as a therapeutic option?
A: Great question; we have not found this to be a problem, but please avoid stress to the extent possible, since patients with mycotoxin-associated cognitive decline are often hypersensitive to stress.



Q: Are we still able to become Bredesen certified? If so, how?
A: Yes, ReCODE 2.0 training is available via Apollo Health. https://www.apollohealthco.com/practitioners/



Q: What would a "cognoscopy" entail at age 45?
A: 3 parts: (1) Blood tests (you can get directly via mycognoscopy.com); (2) on-line cognitive assessment (freely available as CQ test; (3) MRI with volumetrics (optional if you are asymptomatic).



Q: Can you comment on long history of benzodiazepines use and AD and antihistamines use and AD?
A: Yes, both of those have been associated with increased risk for cognitive decline. Anticholinergics, benzodiazepines, PPIs, antihistamines, etc. There are numerous epidemiological studies on this.



Q: Do you test extensively first, then apply appropriate measures, or can one apply some measures without testing, and what are the priorities Dr Bredesen recommends?
A: Best to test first, but you can apply some measures, and then test if/when the measures are unsuccessful. The protocol is detailed in the book, The End of Alzheimer’s Program, and also in The First Survivors of Alzheimer’s.



Q: Have you seen high quinolinic acid for most of the Alzheimer’s participants in the study?
A: Good point. We did not measure this in the study.



Q: Which exogenous ketone do you use? brand name?
A: KE1 is a good one, from KetoneAid. Perfect Keto also has a range of products.



Q: Thoughts about Microwaves, e.g. 5-G, Satellites?
A: It’s concerning. We need a better clinical test to determine who is suffering from this exposure.



Q: What is your preferred source for exogenous ketones?
A: Ketone Aid or Perfect Keto, to name a few. I like KE1. However, if LDL-p is normal (800-1200), you can use MCT oil.



Q: Have you seen burning mouth syndrome, sore tongue/teeth be associated with mold illness?
A: No. Most of the patients we see with cognitive decline associated with mold do not have peripheral CIRS manifestations, although some do.



Q: Do you recommend intranasal antifungal spray, how do you treat?
A: We typically follow the recommendations from Dr. Neil Nathan, detailed in his book, Toxic: Heal Your Body.



Q: Do you think Coenzyme Q10 can help to reduce cognitive impairment?
A: It’s part of the approach to improve mitochondrial function, so it has a role, especially in those with reduced mitochondrial function.



Q: Is there a place for Hyperbaric Oxygen in MCI/Alzheimer's?
A: Yes, especially for those with vascular or traumatic contributions.



Q: How does this tie in with the work of Prof Exley and his findings of aluminum in the brain?
A: Yes, aluminum can be one of many contributors, and amyloid is a metal-binding peptide.



Q: Do you use Cyrex labs Lymphocyte Map to evaluate immune system phenotypes?
A: We have used Cyrex testing (Arrays such as 2, 3, 4, 5, 11, 12, etc.) but not the lymphocyte map—have you found it useful?



Q: What are CNS vital signs?
A: CNS Vital Signs is an on-line cognitive assessment: https://www.cnsvs.com/



Q: What role would intermittent fasting play in therapeutics?
A: Yes, it can be very helpful—helps both to create insulin sensitivity (and metabolic flexibility) and ketosis. There are several other advantages, as well.



Q: Do you think that the treatment protocol works for most other neurological conditions as well such as MS, neuropathy, autism, Restless legs, etc.
A: The protocol is designed for the pathophysiology or pre-AD and AD. It is modified for the different pathophysiologies of these other conditions, and of course it is also personalized so that each person’s optimal protocol will be slightly different.



Q: How can we find clinics and practitioners that are willing to follow your approach in treating Alzheimer's patients?
A: Yes, we’ve trained over 2000 physicians in 10 countries and all over the US. You can check on drbredesen.com or contact Apollo Health staff for a practitioner in your area.



Q: Can you please repeat the name of the person who is utilizing this approach to MCI in San Diego?
A: Several: Dr. Heather Sandison, Dr. Wes Youngberg, and others.



Q: What is the name of the assisted living facility in San Diego that you mentioned is treating Alzheimer's pts with your protocol?
A: Marama (in Vista, just outside San Diego): https://www.maramaexperience.com/



Q: What is the definition of organic toxic buildup? Does he mean metabolic waste that isn't flushing through the drainage pathways?
A: Organic toxins such as toluene, benzene, formaldehyde, and glyphosate can contribute to cognitive decline, in part by reducing glutathione and in part through their effects on mitochondria and other cellular components.



Q: Can you give a link for the ARK Project?
A: No link to this yet; we are still treating the first group—patients with age-related macular degeneration.



Q: 2.0 Bredesen Protocol Health Coach here! Are any practitioners utilizing health coaches with the Bredesen Protocol?
A: Great point. Have you talked with Christine Coward or Valerie Driscoll from Apollo? They may be helpful. Also, most of the practitioners do work with coaches (Drs. Ann Hathaway, Kat Toups, Deborah Gordon, Kristine Burke, Craig Tanio, and many others).



Q: When is he talking about "organic toxins" do you guys think he is referring to metabolic waste buildup?
A: Toluene, benzene, acrolein (see the GPL organic toxins test), formaldehyde, glyphosate, and many other organics. These are also important in Parkinson’s (e.g., TCE, PCE, paraquat, rotenone, etc.).



Q: How can we find a provider using the Bredesen CODE in our area? Thanks.
A: Drbredesen.com or apollohealthco.com



Q: How do you convince someone to start addressing contributors to dementia if you notice MCI, but that person doesn't acknowledge any deficits?
Great point. This is relatively common. Getting all of the family members to have a “cognoscopy” is one way to get people evaluated (therefore the person with MCI does not feel singled out). Good for everyone who is 45 or over to be evaluated and begin active prevention. However, there are some people who simply do not want to admit decline, and it is very hard to treat someone who simply does not want to get better.



Q: Can you provide information about how to learn more about your physician training program?
A: Sure — please check https://www.apollohealthco.com/practitioners/

Increased RANTES, sCD40L and Platelet Aggregation from Genetic and Epigenetic Factors | Bob Miller, CTN

Q: So boosting NO if someone has clots would be bad because it would decrease eNOS and cause further clotting?
A: eNOS (endothelial nitric oxide supports healthy circulation and lowers the risk of clots while iNOS (inducible nitric oxide) creates very large amounts of NO to kill pathogens and inhibits eNOS, thus increasing the chance of clots. For a deep dive into eNOS and iNOS, watch my iNOS interview with Dr Jill Carnahan on her YouTube channel.



Q: How are you measuring thromboxane a2?
A: It’s a urine test from a company called Chronic Inflammation. (www.chronicinflammationtest.com) I’m encouraging Great Plains to try to get back PLA2 and add thromboxane. I believe these two measures, along with checking Omega 3, 6 and AA are very helpful tools.



Q: Do you have an opinion on how the mRNA/lipid nanoparticles may have role in this (vegf maybe) and how those with the vaccines can help supplement to decrease their risks of these long-term effects? Your opinion so far?
A: This is totally speculative and hypothetical, but it would seem reasonable to think any vaccine will stimulate NOX to create immunity. If this stimulates mast cells, histamine and iNOS, this has the potential to activate platelets and VEGF.
To potentially reduce the platelet activation, finding which step in the process may be most active and trying to lower it may be helpful.
I recently did an interview with Dr Jill Carnahan on her YouTube Channel on platelet activation. You may find this useful.



Q: In patients with limited means, is a hsCRP and sed rate enough to rule out systematic inflammation?
A: Its useful, but I have clinically observed individuals with systemic inflammation with normal hsCRP and sed rate, but it can be useful.



Q: What is the easiest way to determine maybe through testing to suspect if a patient has uncoupled eNOS and should not take arginine/citrulline?
A: I am not aware of any specific testing, but clinical observations would be Raynauds or chronic cold hands and feet, high blood pressure (low eNOS) and genetic testing with down regulation of eNOS and gain of function in eNOS or potential mutations in BH4 production.



Q: Can CDP Choline raise TMAO?
A: I’ve seen this happen, so I always combine CDP Choline with Grape Seed Extract.



Q: Do you know about the "omega check" serum test via LabCorp and Quest. If so, do you recommend target levels for protection?
A: Yes, excellent way to see levels. Omega 3 – 8 to 12%. Omega 6 to 3 Ratio 3.1 to 5.1. AA to EPA 2.5-11.1.




Q: If you have SNPs on both FADS 1 & 2, is increased omega 3 supplementation useless; is it better to do Omega 3,6,9?
A: What we are finding to be most useful is oils like Calamari that are higher in DHA, Algae based DHA or if needed, some of the newer supplements that are Protectins and Resolvins. Omega 6 uses FADS first, and can further weaken Omega 3’s turning into Protectins and Resolvins.



Q: Can you expand on why someone with mutations in FAD enzymes can't tolerate intermittent fasting?
A: This has been a clinical observation and we are hypothesizing that since they are not effectively using fats, they need carbs on a frequent basis.



Q: What genetic/epigenetic tests are you using to find the sap's you discussed?
A: We use Functional Genomic Analysis (www.functionalgenomicanalysis.com).



Q: What if you calm the TNFa down with these supplements but the reason that its high isn't removed? Does it cause more damage?
A: Excellent question, as TNF-a is needed to fight off pathogens, so theoretically it could be lowered too much. This is an emerging field, with much to be learned. What we are doing, is trying to lower it when there is a gain of function of TNF-a or excess Iron stimulating. LDN lowers TNF-a so it’s done regularly.



Q: Are you measuring VEGf? What is your opinion of an optimal level?
A: Just started by doing the Covid Long Haul test and considered high when > 12.3



Q: How much resveratrol do you recommend for pathway 1?
A: 250 mg



Q: Can you clarify a few symptoms patients would have with pathway 1, 2, 3?
A: 1 - Possible excess mast cells and histamine, potential inflammation from RANTES. 2 - #2 Hypertension from higher thromboxane, pain and inflammation and activated platelets and ANTES. 3 - Mast cells, histamine.



Q: Thoughts on NAD+ IV for iNOS/eNOS balance and general endothelial function?
A: Here’s a speculative hypothesis. NAD+ creates NADPH that recycles glutathione. If inadequate glutathione, which is needed to clear Peroxynitrite, the Peroxynitrite may lower BH4 which increases NOS uncoupling.



Q: Have you seen low AA on testing? What are your thoughts about this lab finding?
A: Yes, but I am not aware of why or the potential impact.



Q: For people trying to self-regulate blood pressure with diet, would daily consumption of beets be sufficient to over activate the iNOS pathway? Top 3 tips to balance overactive iNOS pathway? What about SOD supplementation to balance the superoxide?
A: 1 - Beets have nitrates that turn into Nitrites that may create nitric oxide that improves the eNOS for healthy blood pressure. 2 - Balance Homocysteine and Iron, reduce histamine. 3 - Avoid Glyphosate as much as possible. 4 - Avoid and clear mycotoxins. <>br>I use SOD quite a bit, but balance with Catalase, or the SOD can make too much hydrogen peroxide. Catalase clears the hydrogen peroxide.



Q: Preferred means of measuring NOX enzyme activity?
A: I am not aware of any lab testing testing that would measure NOX specifically, however the Functional Genomic Analysis software looks at them. Clinical observations may be excess mast cells and histamine. Also, Homocysteine stimulates NOS, so high Homocysteine may be a useful indicator.



Q: How do we get the software he's talking about to use as practitioners?
A: You can get a free trial at www.functionalgenomicanalysis.com

Managing the Complex Patient: Using the GPL-TOX and OAT in Clinical Practice | James Neuenschwander, MD

Q: RE-bone marrow, I have not heard much about using this as a food (lightly roasted for example, from grass fed organic cows) to support patient's own bone marrow function. I read these ages ago, used in childhood leukemia especially. Any thoughts?
A: The issue with bone marrow is that it tends to be high in heavy metals (like lead) even if the animal is raised organically. You would need to use a product that is tested for this. Bone marrow was probably the first animal product humans ate—we were scavengers originally and the only thing left after the lions and the hyenas were done with the animal, was the bone marrow. It is a great source of multiple nutrients if you can find something that is not toxic.



Q: You recommended to continue a long-term detox regimen due to daily exposures. Beyond sauna are there any continued long-term supplementation you suggest?
A: I recommend regular liver detox support (NAC, glutathione, milk thistle, etc.).



Q: Regarding sauna - What about those who react to a sauna or even a hot shower. Do they need to take other steps before they can do a sauna?
A: That reaction is usually from autonomic dysfunction. If it is a detox reaction, then start with binders or Epsom salt baths first.



Q: How do you determine thyroid receptor disruption? Clinically, and check organophosphates?
A: Most toxins will disrupt thyroid function, so that is a given. There is no test I know of to test thyroid receptor function—a patient would have a low basal body temperature with normal thyroid numbers and no other explanation.



Q: Can toxins be the cause of burning mouth syndrome? Painful throbbing teeth? Thanks so much.
A: Burning mouth is an autonomic dysfunction along with some type of neuropathy. You have to figure out why. Toxins are always on the list for this.



Q: Can toxins affect free testosterone levels, as well?
A: They will affect production of testosterone. The amount of free testosterone is so miniscule, I am not sure if they will affect this directly outside of affecting total testosterone. I do not know if toxins impact albumin or sex hormone binding globulin (I have not read anything on this)—these are the two proteins that bind testosterone.



Q: I have a patient with elevated MTBE #1 on GPL tox - drinks only bottled water, lives in rural suburb near pond. Any recommendations on looking for source? Any other ideas on detox other than liposomal glutathione and NAC? Thanks.
A: MTBE is ubiquitous. Have they checked the bottled water? None of that is regulated — I can fill a bottle from the tap and sell it with any label I want. If there is not obvious source, work on the liver.



Q: Do you recommend IV chelation? or use of binders?
A: I do IV chelation for heavy metals—this was not covered in my lecture. I use binders—that was part of my lecture.



Q: What reference range do you use for reproductive hormones? As you know, reference ranges vary from test to test. Also, hormone levels vary depending on where patient is in their menstrual cycle, or arguably even time of the day.
A: I would recommend doing a course in hormone replacement for this answer. Ranges completely depend on where a patient is at in life, their menstrual cycle, and where their base line was. It is usually a range of okay along with managing patient’s symptoms.



Q: What do you say to a patient that won't change the exposure? Do you still treat them? Can treatment compound the problems they have?
A: Unless it is a temporary situation, I won’t treat them. It is like treating a patient with cardiovascular disease or diabetes that won’t change their diet or lifestyle. That is why we have traditional physicians—they would be more than happy to prescribe drugs for the rest of their lives. I don’t waste my time. If someone doesn’t want to get better, you can’t make them. Move on.



Q: If it’s determined that a patient has low glutathione recycling due to SNP and this likely the cause of presence of toxins-can they take glutathione long term without negative consequence?
A: Be careful with SNPs—there are very few that are determinate. Low glutathione has many causes, one of which is recycling. If you are going to use SNPs, you better have the entire glutathione/sulfation/uric acid/methylation/ammonia cycle SNPs laid out to see the entire pattern. Using a precursor (sulforaphane and/or NAC) first will tell you if you need to use glutathione itself. If those two do not increase the level, then I will use glutathione chronically.



Q: Toxicity of microwaves how significant is this? Seems to be coming way too high.
A: EMFs are a topic all by itself. I am not an expert on this, but the literature I am read suggests that it is a problem.



Q: What do you think about silicon rich water to reduce aluminum levels?
A: The problem with products like Fiji water is that come in plastic bottles and are shipped from Fiji. I typically use a supplement for this (like BioSil).



Q: Any specific suggestions to help detox glyphosate?
A: Binders are an effective way to detox glyphosate as are saunas.



Q: Do you think mitochondrial nutrient support is helpful, at the same time as detox?
A: Yes, most of our chronically patients have mito issues. The ultimate solution is to eliminate the cause of the cell danger response.



Q: Are saunas safe for kids? what age?
A: Yes, I reserve the lower age for children that can express their needs (usually around age 3). Things like headaches or dizziness are signs that they are not tolerating. Start low and go slow.



Q: Do you have a supplement recommendation for blood sugar dysregulation due to toxins for someone who eats clean, has mold, and still needs help getting A1C normal again? Is it just a matter of time?
A: Detox the mold first to see where the patient is at before working with other medications or supplements for the sugar.



Q: Can NAC or glutathione be used long term?
A: NAC - yes, Glutathione — usually, but not something that I like to do.



Q: Do you believe after filtering water through zero water you need to replenish with minerals?
A: That would be ideal, but I tend to take and recommend mineral supplements

The Clinical Approach of a GPL Consultant on GPL Testing | Jasmyne Brown, ND

Q: Dificid is recommended first line therapy for C diff with fewer side effects than Flagyl or Vancomycin. What are your thoughts?
A: do not have much experience with that antibiotic and how it influences the clostridia markers on this test. However, the OAT does not necessarily differentiate between the pathogenic clostridia species. There are a number of pathogenic clostridia species, and by measuring various metabolites produced by these organisms, you can cast a broader view of pathogenic clostridia that would otherwise not be identified on a stool test. With that said, the intervention is dependent on how aggressive you as the practitioner see fit. Interventions vary from high dose (generally between 10-12 billion) spore- based probiotics to botanicals to pharmaceuticals.



Q: Is GPL Labs doing DBH testing? if not which lab provides the testing for copper- polyuria?
A: GPL is not currently measuring DBH. The best way to assess it, at this time, is either through genetic testing or a spinal tap. We do measure copper (along with ceruloplasmin and zinc) via serum https://www.greatplainslaboratory.com/copper-test-1 and via urine through the heavy metal urine test https://www.greatplainslaboratory.com/metals-urine-test.



Q: How do you time your treatment of a patient with mold, SIBO, IMO, Candida, dementia, and oxalate kidney stones? What is your protocol including prescription medications and supplements?
A: This is highly dependent on the patient, and multiple other factors.



Q: Do you recommend to-do DMSA and Glutathione provocation prior to ENVIROtox?
A: DMSA provocation is only necessary for a heavy metal urine test. Glutathione is not recommended for any of the test on the ENVIROtox (Glyphosate, GPL-TOX, and MycoTOX Profile) as the ranges are based on people not provoking.


Day 3 Q+A: Health Implications of Mold, Environmental Toxin Exposure, and More

Click each presentation title to expand the answers from each speaker.

Environmental Toxins and Prenatal Care | Joseph Pizzorno, ND

Q: How do you approach patients with abnormally low GGT who may have difficulty recycling glutathione?
A: Very good question! And one I have been thinking about and have not figured out a good answer. At this time, I recommend topical or liposomal glutathione.




Q: What are some safe brands for cooking pans?
A: I have not independently evaluated specific brands so can’t make an informed recommendation. We use the new ceramic cooking ware. Appears to not leak toxins and is reasonably easy to clean.




Q: How long do you need to eat organic/limit exposure to see a change in blood work or on other toxin screening tests? / How long would you wait until retesting?
A: Remarkably, blood and urine pesticide levels drop dramatically—75-90%--after just 4 days of eating organically. The problem, of course, is that most are fat-soluble, so they accumulate in the fat. Since blood and urine change so quickly, I recommend testing 2 weeks after the patient tells you they have been eating organically.




Q: If I wanted to grow my own organic garden, where do you get seeds? Are the seeds in a typical store organic?
A: Happy to report there are a lot of good sources! I prefer the seeds to be both organic and heirloom. I like most of the food produced by the seeds I get from Uprising Seeds in Bellingham, WA.




Q: What natural sequent do you recommend?
A: All food-sourced fibers. Unfortunately, very little objective research. The little that is available is mostly wheat and rice fibers. Considering that most people react adversely to wheat, I suggest rice. And yes, good idea if you can get the manufacturer to document arsenic free.




Q: How does exercise with sweating compare with sauna for excreting toxins? Do you recommend red sauna or the blankets?
A: I asked the great researcher Steven Genuis, MD this question. His response is that it doesn’t matter. All that matters is the sweating.




Q: Is NAC ok for pregnant women?
A: I believe <1,001 data-preserve-html-node="true" data-preserve-html-node="true" mg/d should be safe for everyone. The only reactions I have seen are in a very small percentage of people who have a sulfur metabolism problem. Watch for IBS, acid reflux and/or allergies as an indication of sulfur overload.




Q: I'm working in community that has several paper mills. What toxic burden does that present to the people?
A: Highly dependent upon the source of the materials used. Unfortunately, trees will incorporate toxins they are exposed to. For example, if grown in an area with mercury contamination, the trees will be high in mercury which is released if there is a forest fire. The only way to be sure is to go to the US Geological Service website (www.usgs.gov). they’ve a large number of maps by county of the many toxins in the environment. Also, the Environmental Working Group has a website where a Zip Code can be entered to determine the toxins in the area.




Q: What is the half-life of PBDEs? How can we get them out of the house/off the floor?
A: I have not been able to get a good answer on this. Appears to be months, but I am not sure. The research does show that the more brominated the PBDE the longer the half-life.




Q: Do you have a resource on the half-lives of specific toxins? Thanks
A: I found a great paper that has many of them, but not all. Also includes a lot of drugs. Therapeutic (“normal”), toxic, and comatose-fatal blood-plasma concentrations (mg/L) in man. 150 pages and almost 1,000 references. Very useful.




Q: What is the most reliable test for metals if you cannot do provocation before testing?
A: Depends upon the toxin (lead—blood, cadmium—urine, arsenic—urine, mercury—urine.). But must recognize the “safe” standards are way too high. Urines should all be first morning.




Q: Dr. P, What about a low GGT? Does this mean liver needs more support?
A: They likely need glutathione. Measure their RBC glutathione.




Q: Doesn’t ggt also assess gallbladder function? In the ICU, we used to check ggt when we suspected gallbladder disease, which makes sense that it’s elevated when they are not detoxing well d/t gallbladder disease...
A: Yes, there are several causes of elevated GGT. Need to determine the full context.




Q: Is GGTP the same lab test as GGT?
A: Yes. The same test but labs use both abbreviations.




Q: Can you repeat the name of Doc in Northern CA who follows the GGTP?
A: Alan Goldhamer, DC measures GGTP in his fasting clinic.




Q: Does 8-ohdg also measure damage from mitochondrial dan?
A: Good question! And one I have wondered about. 8-OHdG has been used for both nuclear and mitochondrial DNA damage but I have not been able to quantify the differences. We do know that mitochondrial DNA suffers a lot more damage and does not have the repair mechanisms of nuclear DNA. So, I would not be surprised if the urinary markers are dominated by mitochondrial damage markers.




Q: Do you think the Big Berkey water filter is enough? Or what about distilled water, with adding minerals?
A: I do not at this time have enough data to compare manufacturers. Distilling water and adding minerals is a good strategy.




Q: Do you think fiber in food is enough, or do you recommend fiber powder?
A: Hard to get enough fiber from diet unless eating primarily vegetarian and primarily high fiber foods. Supplemental fiber seems a good idea to me.




Q: A great resource for parents is Lead Safe Mama website https://tamararubin.com/ information on lead in children's toys, dishes, etc.
A: Great! Thanks for sharing.




Q: How long should a gal wait to get pregnant following removal of amalgams by an environmental dentist?
A: Assuming active efforts to avoid all other mercury sources and active facilitation of excretion, 6 months will get rid of most of the mercury.




Q: Can you comment on what pollutants we should be concerned with near a landfill in US?
A: Not being facetious — all of them.




Q: What key lab tests should a woman who has had 3 miscarriages in the first trimester have done before getting as part of her prenatal and fertility care?
A: Homocysteine, methylmalonic acid, GGTP, 8-OHdG, blood lead, and urinary mercury.




Q: How do you filter outside air? Isn’t that where your furnace and AC gets the air?
A: Depends upon the installation. The furnace typically recirculates the air of the house and has a separate intake to bring in outside air for the burning. Opening a window lets in outside air. If heavily polluted area, then should consider clearing outside air before it enters the house.




Q: Please tell us some of the toxin-absorbing plant names?
A: Moss case, Pot mum, Gerber daisy, Warneckii, and Ficus.




Q: With use of plants do you increase exposure to soil spores?
A: Probably, likely.




Q: What do you do when people are non-sweaters?
A: More fiber and glutathione.




Q: Does sweating from exercise and/or hot tub excrete these toxins as well?
A: Yes. Note that hot tubs and steam baths recirculate toxins unless removed by a filter.




Q: I have patients who barely sweat, they go in sauna and don't sweat until have been in there for at least an hour...thoughts on this?
A: Trickly. I can’t recommend specific protocols without knowing more about the patient.




Q: Do you have a recommendation for trace mineral supplementation?
A: Eat organically grown foods. No specific supplement recommendations.




Q: Do you recommend drinking alkaline water while in the sauna?
A: Theoretically, yes. But I’ve no research. The sauna drink I make for myself is slightly alkaline.




Q: Are saunas safe for kids? what age and time limit?
A: Yes, and a bigger question than can be answered here.




Q: What are your thoughts/recommendations for those that don't tolerate sauna (or even hot showers/baths) without feeling ill?
A: Primarily Red face, elevated heart rate and dizziness. Is it possibly related to histamine intolerance? This question has come up a lot. I will give it more thought.




Q: Is there an optimal reference range for GGTP?
A: My best estimate at this time is 15-20.

Non-Metal Toxic Chemicals and Their Effects on Health: Glyphosate and Beyond | William Shaw, PhD

Q: How toxic is weed/cannabis these days? I got a feeling it's loaded with metals and chemicals with cadmium leading the way. Does excess weed-smoking keep the copper/Dopamine high?
A: Acetaldehyde, ammonia arsenic, benzene, cadmium, chromium, formaldehyde, hydrogen cyanide, isoprene, lead, mercury, nickel, and quinoline are common in cannabis. Those who exclusively smoked marijuana had higher blood and urine levels of several smoke-related toxic chemicals such as naphthalene, acrylamide, and acrylonitrile metabolites than non-smokers. Metabolites of the last 2 chemicals are tested in the GPL-TOX test.




Q: Does your lab offer any tests for toxicities of chronic Lyme disease?
A: No.




Q: Do touch screens on electronics increase risk of exposure to chemicals?
A: Triphenyl phosphate is a significant hazard on computer screens, touched or not.




Q: Which brand of household cleaners would you recommend?
A: Don’t have one.




Q: Any suggestions on best ways to detox patients who are getting significant number of IVs? Or for anyone getting IVs - should they be taking binders for a particular amount of time before/after? any suggested protocols to detox the plastics?
A: Plastic IVs are all potentially hazardous. Request glass containers instead. Sauna is the best treatment.




Q: 1-bromopropane could be used for foam gluing. Is foam mattress and foam pillows for sleep also big source of? Are older foams better or worse?
A: Good question but don’t know.




Q: Dr. Shaw mentioned that glutathione will detox many toxins. If we start a patient in which we suspect a heavy toxic load on glutathione, are we in danger of seeing a large enough dump to see a severe herx reaction?
A: Most glutathione adducts are less toxic than the original toxic chemical not attached to glutathione. There are exceptions so there could be an occasional toxic reaction. Since there are tens of thousands of toxic chemicals there is no comprehensive source of this information.




Q: How does urine neurotransmitters rate to brain levels? Do they correlate?
A: Urine neurotransmitters correlate to brain levels since the same enzymes are present in both central and peripheral nervous systems for dopamine, epinephrine, and norepinephrine.




Q: Dr Shaw which supplements. do you take?
A: CDP choline, lithium, vitamin C, B6, methyl folate, methyl cobalamin, carnitine, biotin, Vitamins A, D, and K.




Q: What brand of air filter system do you use in your home?
A: None right now.




Q: What other techniques other than supplements and air filtration do you do to keep your toxins low?
A: The main thing is organic food and reverse osmosis water.




Q: Any suggested brands of sauna? Red sauna or blanket?
A: The only sauna not recommended are those made of pine which off-gas terpenes when heated.




Q: Will water distillers remove the vinyl chloride from the PVC in nearly everyone's home and workplace?
A: Reverse osmosis systems are the only systems that remove almost all chemicals.




Q: When you mention acrylic fibers being carcinogenic-does that include clothing-so much is made from acrylic?
A: Yes, if the person is exercising, the chemicals may off-gas and enter the skin.




Q: I am now wondering how many crafters who are big into the yarn arts are at risk, since there are many yarns that contain acrylic. It would be difficult to do yarn arts wearing gloves. Any advice?
A: Acrylics and other synthetic fabrics would be most toxic when wearing them while hot so they might off-gas.




Q: Can people with a sulfur allergy take glutathione?
A: A sulfur allergy would have to be defined. Virtually no one except industrial chemists are exposed to pure elemental sulfur. Two sulfur-containing amino acids found in almost every protein are cysteine and methionine. Virtually every normal person has high amounts of sulfur containing glutathione. I don’t think someone who is severely allergic to these amino acids could be alive. Some people mean they are sensitive to sulfur containing antibiotics. I seriously doubt that anyone is allergic to glutathione since it is present in virtually every cell in the body. If unsure, put a drop on the skin and see what happens.




Q: Is there an exhaustive list of where each of the environmental toxins are found? if so, where? i.e., work exposure with certain chemicals....
A: The Great Plains website is a good place to star. In this brochure, pages 10-15 are fairly good sources.




Q: Did any ALS patients who you highlighted in the lecture improve with removing exposure, sauna and NAC/Glutathione treatments?
A: Haven’t had time for follow-up. Biggest impediment is that family members consider ALS incurable so don’t want to treat.




Q: Many students are now using iPads that you can write on. Do you feel that the coating on the screen is being absorbed into the hands while writing or is the risk more with inhalation from off gassing?
A: Don’t know.




Q: Are latex gloves without powder toxic?
A: The latex allergy is to the gloves themselves not the powder.




Q: Are you of the opinion that glyphosate is one of the main causes of the rise in autoimmunity, due to alterations in protective microbiome? It's been sprayed on wheat/oats for 25 years and gluten is proven autoimmunity trigger.
A: Yes. Many articles on this. Wu HJ, Wu E. The role of gut microbiota in immune homeostasis and autoimmunity. Gut Microbes. 2012;3(1):4-14. doi:10.4161/gmic.19320




Q: Thoughts on the use of fermented foods such as sauerkraut packaged in plastic?
A: Plastic packaging is a big problem for all foods.




Q: A lot of people get Culligan water delivered to their home in big plastic jugs.... would it be better for them not to do this?
A: I am one of these people and need to ask what type of plastic is being used.




Q: Please can you repeat and expand on how Norepi influences in immunity after vaccination?
A: Clostridia bacteria phenolic metabolites inhibit the conversion of dopamine to nor-epinephrine by dopamine beta-hydroxylase. Since nor-epinephrine is needed to mount an immune response, the vaccinations don’t work if norepinephrine is deficient. Alaniz RC, Thomas SA, Perez-Melgosa M, Mueller K, Farr AG, Palmiter RD, Wilson CB. Dopamine beta-hydroxylase deficiency impairs cellular immunity. Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2274-8. doi: 10.1073/pnas.96.5.2274. PMID: 10051631; PMCID: PMC26773.




Q: Can you comment on cancer chemo / immuno drugs and chemical type of toxicity? At what point is it appropriate to test?
A: Many chemotherapy drugs are mutagenic. Organic acid testing might be useful to assess negative effects of chemotherapy.




Q: Not classical toxicity, but what evidence do we have of the biology of intense sensitivity to minute quantities of, salicylates, terpenes, non-pigment pill fillers...doesn't seem like histamine or IgE related? Hard to use herbals in such patients.
A: Many pharmaceuticals use phthalates as a time release agent. Not a good thing to do.




Q: What is the half-life of xylene?
A: Based on the rate of elimination of m-xylene in expired air, the half-life was 0.8 hours for the initial phase, 7.7 hours for the intermediate phase, and 17.7 hours for the slowest elimination phase. Overall, the elimination half-life of m-xylene from subcutaneous adipose tissue has been estimated to be 58 hours in a man.




Q: How long after painting your inner house are toxins reasonably less to live there?
A: I would say when the odor is no longer offensive. Or use “green” brands of paint.




Q: Why do so many supplements come in plastic bottles, eg the GSE of New Beginnings?
A: Glass would be better, but it breaks in shipping.




Q: Are phthalates what are off gassed in new cars and what would you recommend for people who have a new car and therefore continuously exposed besides binders and NAC/glutathione?
A: The chemicals of the new car smell are ethylbenzene, formaldehyde, and toluene.




Q: Are you aware of any water filtrations systems for the home that would filter out vinyl chloride?? Many newer homes are plumbed with plastic now, no longer copper.
A: You would likely need reverse osmosis.




Q: Can you comment on what toxins you see with vaping?
A: A vape website lists the following: Diacetyl: Inhaling diacetyl has been linked to irreversible lung damage in factory workers, according to the National Institute for Occupational Safety and Health (NIOSH). Heavy metals: Exposure to heavy metals may cause flu-like symptoms, lung damage, and even cancer in some cases. Ultrafine particles: If inhaled, ultrafine particles may damage the respiratory and cardiovascular (heart) system and other parts of the body. Volatile organic compounds: These compounds including acetaldehyde, formaldehyde and acetone may put people at risk for many health problems, such as cancer and heart damage.




Q: How were the percentile data derived? From NHANES or from GPL? Do the percentiles relate to a "healthy" population (however that's defined!) or a general population? If the latter, how was referencing based on a biased population avoided?
A: 3The percentiles were directly taken from NHANES which attempts to provide data on a normal population. They are not gathering data from patients in hospitals or clinics.




Q: What about toxins in tattoos?
A: 3A consumer group warned of the "the presence of carcinogenic, neurotoxic or highly allergenic products" in three-quarters of inks most used by French tattoo artists, French newspaper Le Monde said in a report. Colored inks can contain lead, cadmium, chromium, nickel, and titanium. These metals can trigger allergic reactions and potentially lead to disease.




Q: When GPL-TOX levels are not elevated greater than 75%tile or 95%tile, but many or some markers are less than or equal to the 75%tile does synergy does take place? Does this suggest increased toxic body burden?
A: 3You are right. Multiple exposures below the 95th percentile might be as hazardous as a single chemical above the 95th percentile.




Q: Can you comment on 3M claims they have a replacement for 1-bromopropane and TCE?
A: 3M™ Novec™ Engineered Fluids are non-flammable fluids used in a wide variety of industrial applications, including vapor degreasing, solvent cleaning of industrial parts, and thermal management of electronics. Claims have been made for better safety for this product. Time will tell.




Q: What are the major differences between Glutathione vs. NAC?
A: NAC is a precursor of glutathione and may be absorbed from GI tract more readily than glutathione although liposomal glutathione is well absorbed.




Q: Do these pathogens show up on stool studies that are designed to find them such as those from Genova Diagnostics or Doctors Data? I’ve rarely seen these pathogens on those studies.
A: The OAT test of the Great Plains Laboratory is the best (and only) test for detection of Clostridia bacteria that inhibit dopamine beta hydroxylase. It is better to ignore the Clostridia sections of other labs,




Q: How much of an influence does glyphosate/toxins have on MS and autoimmunity in general?
A: See question 22. Many patients with MS have high toxic chemicals.




Q: What is the half-life of 1-bromopropane? What is the half-life of 3-HPMA (acrolein)? Can we have the half-lives indicated on the GPL-TOX reports? That would help us tremendously!
A: Wistar male rats were exposed to 1-bromopromane (1-BP) vapor for 6 hours a day, 5 days a week, for 3 and 4 weeks (1500 ppm) and 1 day, and 4 and 12 weeks (700 ppm). ... 1-BP in blood decreased rapidly to the detection limit within 0.7 hr. On the other hand, bromide ion persisted longer in both blood and urine; the biological half-life of bromide ion was 4.7-15.0 days in blood and 5.0-7.5 days in urine. : Urinary 3-HPMA levels from acrolein were increased after 2-hr consumption of fried food with an elimination half-life of 10 hr. Human data are not available for 1-bromopropane. I will start looking for the other compounds. PMID:12191883 Ishidao T et al; Toxicol Lett 134 (1-3): 237-43 (2002)




Q: Can an OAT test's results be within normal ranges and the GPL-Tox or MycoTOX Profile have elevated values?
A: Yes.




Q: Do more "clean" tobacco sources, such as American Spirits, offer much improvement to the multiple toxicities associated with tobacco exposure?
A: American spirits do not contain glyphosate but its smoke has all the same harmful chemicals as any other cigarette.




Q: Which type of sauna do you recommend for most effective treatment in removal of toxins?
A: Any except those made from pine.




Q: Have you seen increased toxic load in your patients who have received the Covid vaccine?
A: I haven’t analyzed the data.




Q: What is the scientology sauna protocol?
A: The protocol can be accessed at the following link: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259397/pdf/10.1177_0300060518779314.pdf

The Role of Other Toxicants in Mold Patients – How to Assess and Treat | Lyn Patrick, ND

Q: Do air pods emit EMF's? Kids wear them all day long.
A: Yes, they do.




Q: Can Dr Patrick repeat the suggested dose for NAC? Thanks!
A: I mentioned this during the talk so it will be on the recording- adult dose is 1800-2500 mg contraindicated in peptic ulcer.




Q: Will an air filtration machine with a Hepa filter remove aerosolized printer ink?
A: Depends on unit look for the filtration capacity- ultimately you want a unit that filter down to .003 microns




Q: Do we presume, or is there evidence, that all people with positive mycotoxin tests are colonized and/or have biofilms?
A: No evidence UNLESS there is no obvious sign of exposure meaning (home/workplace/school tests negative for mold and mycotoxin yet symptoms persist. My colleague Neal Nathan who knows much more about this than I do does not recommend nasal washings for culture due to false negative findings and recommends treatment in the above case.




Q: What about PEMF use? Can it mitigate EMF effect?
A: I would ask you to think about EMF/EMR like you think about tobacco smoke- would you recommend a vit. C therapy for smoking patients and not also intervene w cessation strategies? PEMF is helpful but mitigation involves remediation (hard-wiring, avoidance of Wi-Fi, keeping phone away from body or off, etc.).




Q: Do you recommend any of the protective EMF wearable devices?
A: Clothing that is penetrated with silver wire is protective, if you mean a device like a magic dot or other applications, no evidence.




Q: Vitamin E- do you recommend taking just tocotrienols or the full spectrum with tocopherols? There are some good literatures about benefits of just tocotrienols for cell membrane health and oxidative stress.
A: Vit. E, like vit. C is a complex of related compounds: gamma, alpha, beta, delta tocopherol and all four tocotrienols are necessary.




Q: Are using traditional headphones or Bluetooth headphones just as damaging as putting your phone to your ear?
A: Don’t know what you mean by traditional headphones, there are air gapped external earbuds that are OK to use but anything that allows a signal to go to your ear/skull/brain is damaging.




Q: You mentioned high prolactin as being from pesticides? How would you manage this in your pt?
A: The actual data on this comes from pesticide applicators who are occupationally exposed- treatment for OP toxicity involves B complex and high levels of antioxidants (C, E, Se, Zn, ALA, GSH, NAC, melatonin especially). OPs have short ½-life in body so further avoidance is crucial. Of course, other psychologic stressors can also raise prolactin so that must be addressed as well.




Q: Can Ozone break down the forever chemicals?
A: No, the fluorine/carbon bonding is the problem not vulnerable to ozonation.




Q: Does putting a device on airplane mode reduce EMFs?
A: Yes, it does there is still some small residual exposure but most of it comes from the phone searching for a signal.




Q: What is your opinion about using alkaline water in machines (such as "Kangen" machines) to remove pesticides from vegetables or using as drinking water? Would this result in removing beneficial bacteria from the gut?
A: I thought the US Consumer Protection Agency made Kangen illegal to import into the US I didn’t think they were still available. Water cannot hold an alkaline charge, it’s the minerals in the water that determine pH. Cheaper to just add mag glycinate to your water, no? Vinegar is highly effective at removing pesticide residue from fresh fruits and vegs, Dr. Pizzorno had an entire slide on that protocol. Cheaper as well.




Q: How about glass IV bottles from McGuff pharmacy?
A: We used to all our IVs in glass bottles in the old days, I do disagree w Dr. Shaw about phthalate contamination from IV bags, I think they have to be heated to contaminate IV w phthalates.




Q: I heard an ND say that toxins are stored in the bones too and not just fat tissues, but I have never heard that before - Is that true?
A: Depends on toxin- lead, cadmium, per fluorinates are stored in bone, the science on that is clear.




Q: I heard from a mold specialist that some 'mold' (Penicillium) is only introduced from Pharmaceuticals - Is this true?
A: No, look at my slide from EPA identifying molds commonly found in buildings.




Q: Thank you for bringing up EMFs!!! How about the recent satellite launches since 2020?
A: See this article that was just published a few weeks ago- measuring ground level EMF/EMR from small cell towers- they are source of the radiation not satellites: https://www.spandidos-publications.com/10.3892/wasj.2022.157.




Q: Do Sleep number beds increase your risk of EMF exposure significantly?
A: I had to look this one up (LOL). Obviously if you can program them remotely they are receiving a signal. You would have to use an EMF meter to quantify the v/M or microwatts/cm2. (Safe Living Technologies has a good meter.




Q: Do you think using a keyboard and mouse is safer than touching the IPAD itself?
A: No same exposure, safest is a hardwired external keyboard and mouse a few feet away from computer




Q: Where can we get more training on how to evaluate patients on EMF exposure and possible treatments for them?
A: We have a free lecture on our training website: emeiglobal.com and the emfconference2021 has CME courses as well.




Q: Could we get the name of the EMF study that Dr. Patrick is referring to in her lecture?
A: PMID: 32168876 let me know if this isn’t the one you wanted




Q: What is the best way to protect against EMF? Do you recommend products from Aires Tech or similar companies? NO please go to EMFConference2021 and see CME education courses for doctors as well as my course at emeiglobal.com
A: There is no magic pill for this- sorry. All of the Aires Tech “scientific papers” were peer-reviewed in house, and none were published in actual peer-reviewed journals. Grounding and PEMF helps but does not substitute for remediation.




Q: Regarding covid, anxiety, and EMF, both can stimulate mast cells, NO/ONOO activity, kynurenine, NMDA activity, etc. How relevant do you feel this has been over the past 2 years, even though everything is being blamed on covid?
A: I am very concerned about EMF hypersensitivity which has many of the same symptoms as Covid-19. Please follow Dominique Belpomme MD, a French oncologist who has published clinical data on this in his patient population of electrosensitive/chemically sensitive population.




Q: How do you propose we evaluate someone's EMF sensitivity?
A: Here is a free YouTube by a physician from the UK- Erica Mallary-Blythe MD, who covers how to diagnose during an office visit: https://youtu.be/_iP-Zv3VLV4.




Q: Should the router be turned off at night?
A: Yes, if not hard-wired it is important to turn off the router at night.




Q: Is there any research showing that cellphones used in the car have stronger negative effects?
A: Cars act as small Faradays cages catching and holding in EMF, especially signal cell phone generates so yes exposure is worse in an automobile.




Q: Can you comment on how to protect from EMF exposure with hearing aids?
A: Turn off Bluetooth that connects hearing aids to your phone.




Q: EMF question- Are wireless headphones a big source? More dangerous due to proximity to brain?
A: Yes, Bluetooth is more exposure than regular headphones, air gapped headphones are best, easily available through online vendors.




Q: Can you comment on urine iodine testing? Endocrine tells me that neither serum or urine iodine testing is accurate. What reference range should we target?
A: Depends on reason you are testing, anything less than 200 mcg in urine is deficiency according to standard medicine.




Q: What are the ways to support the body & or reverse these effects of EMF for our children?
A: 1 - Cell phones should be kept 3 feet away from body (use speakerphone). 2- No devices in bedroom at night. 3 - Turn off router at night. 4 - Deal directly with internet and device addiction in children.




Q: Do you have any Canadian sources for labs that test for PFAS?
A: Sorry, I do not- use the PFAS sites I talked about for resources.




Q: What labs companies that will check my water that also includes MTBE?
A: Watercheck.com call them if it’s not on the website they can look for almost anything.




Q: Can you repeat the name of the researcher who is doing PFAS and Covid?
A: Phillipe Grandjean PhD




Q: If fish are high in PFAS would fish oil supplement be counterproductive in supporting health?
A: As you know good fish oil undergoes a process of distillation to remove POPs (PCBs, organochlorine pesticides) and can remove PFAS please ask your fish oil manufacturer for a Certificate of Analysis for PFAS, very few will be able to provide it.




Q: What are the most common toxins used on golf courses in the USA? Glyphosate and 2,4-D?
A: Golf courses have 2-4 times the pesticide use of agricultural land, herbicides are commonly glyphosate-containing but yes 2,4-D as well.




Q: Could you comment on the use of apheresis use for chemical and other toxins?
A: Therapeutic apheresis for chemical toxicity is only available in Germany right now and one or two places in U.S. I have never had to use it if able to use sauna, colonics, IV nutrients, chelation.




Q: Does plasma donation help with detoxification of any of these toxins?
A: Yes, it does lower blood levels of PFAS, this has been published by Stephen Genuis MD.




Q: I've heard that using Data on your phone is less EMF exposure than WIFI. Is this true?
A: Yes, cellular data doesn’t have same exposure as phone searching for a Wi-Fi signal.




Q: Does the blood removed from phlebotomy treatment for pfas get donated? Do you have to let know not to use the blood?
A: You are way ahead of the rest of the medical world, but no one can’t donate blood and then tell the blood bank not to use the blood, they won’t listen to you.




Q: Would you please repeat the company name who is using plant based can lining?
A: EDEN foods.




Q: Can you comment on natural cholestyramine alternatives as a binder for PFAs and other toxicants, such as beets and okra?
A: Sorry for any confusion but CSM is only agent that has been shown to reduce PFAS, foods will not do it Genuis also published this data.




Q: Milk cartons - are they a source of BPA type exposures? Is the fact that milk is cold a reliable protector for humans, or are we getting gradually poisoned by such packaging?
A: BPA in food contact materials: cans (beverage and food), hard plastic water bottles, no BPA in tetrapaks (milk, soymilk, almond milk, etc.).




Q: Melamine is frequently used in children's dishes. Is melamine also toxic even if not microwaved?
A: No




Q: As an ND, I love castor oil packs for detox. Is that something you still recommend?
A: Sure, castor oil increases lymphatic flow, but then lymph has to clear blood, kidneys and intestines.




Q: What is your optimum cholestyramine dose and frequency of dosing?
A: Standard dose 4 grams qid, not realistic for patients due to need to dose in between meals. 4 grams bid at bedtime and on waking will do the job.




Q: Where can we find more of your past and future webinars online?
A: Emeiglobal.com or National Association of Environmental Medicine (envmedicine.com) we also have some lectures on YouTube.




Q: What is the lab that measures PFAS for free? What is the lab that measures BPA?
A: PFAS for free will be done by public health depts. If local water levels are high otherwise no free testing. Millionmarker lab does BPA, BPS, BPF.




Q: Did you know Theo Colborn? Please let me know.
A: Yes, Roy I was fortunate to spend time w Theo for a few years before her death, we both live in gas and oil fracking areas in CO, and she was very active in addressing exposures from fracked gas and oil wells. I was very fortunate to know her as a colleague and friend, feel free to email me.




Q: What suggestions would you have for those with histamine intolerance or mast cell activation disorder and want to use a sauna? (Generally, heat can cause issues in those disorders)
A: Bowel tolerance vit. C (L-ascorbate like that made by Perque) or using C Cleanse and luteolin Also keep heat down around 100.




Q: Do you think we should take glutathione every day for the long term? Or should this be in bursts?
A: No idea why “bursts” would be a good idea, please explain that. Oxidative stress is constant so- no glutathione = massive oxidative damage = mitochondrial damage = tissue and immune damage.




Q: What is your opinion regarding the work of the Weston A Price Foundation?
A: Theoretically eating ancestral diets is a great idea. Sadly 80 years of persistent pesticides and organic pollutants like PCBs and PFAS have caused mammal fat to be a depot for toxicants. Butter, farmed fish, and beef have high levels of PCBs: cardiotoxic, immunotoxic, thyroid disruptors, reproductive toxicants.

Identifying and Treating Complex Patients with Mold Toxin | James Neuenschwander, MD

Q: Does freezing foods 24 hours (like grains, nuts, and coffee) kill the mold?
A: The issue is not the mold in the food—it is frequently not there due to processing. The issue is with the mold toxin. Freezing food does not destroy mold toxins. Only cooking to temperatures over 500 degrees will destroy most mold toxins




Q: Have you seen a patient with a VCS that is normal with an OAT or Mycotox that is abnormal?
A: Yes. The presence of a mold toxin does not mean that the person is reacting to it. Most people can have mold toxins in their system and not be sick. The Mycotox would be abnormal with a normal VCS. The OAT is a bit more complicated. Mold markers on the OAT are an indicator of colonization—this is abnormal, and a person is going to have an abnormal VCS—I don’t think I have seen a normal VCS with an abnormal OAT.




Q: Do you have a recommendation for a good vagal nerve stimulator?
A: I have not had great success with these. The one I use is the Alphastim—it clips to the ear lobe. It can also be used peripherally for localized pain.




Q: Are those that are most sick usually have the genetic predisposition? Sometimes when test couples when one has cognitive decline, other spouse feels normal but has exposure on testing.
A: Cognitive decline is almost always linked with ApoE4 variants (along with ApoC1 and TOM40 variants). This has to do with the brain’s ability to detox. Illness is always the intersection of genetic predisposition and the environment. Enough toxicity and everyone gets sick (think Hiroshima). Little enough toxicity and no one gets sick. Everything else is on a bell curve.




Q: Could low serum sodium secondary to mycotoxins be due to suppressed aldosterone?
A: Yes. This would typically be tied to low cortisol and ACTH levels (measure aldosterone in the morning along with cortisol). For most of my mold patients, the issue is not the adrenal cortex (aldosterone) but pituitary signaling (low AVH). Almost always, I will have a high osmolality and low AVH. Low aldosterone would specifically lower sodium but shouldn’t raise osmolality.




Q: Do you have a MARCON test that you recommend?
A: I think the lab we use is MicrobiologyDx—we do the swabs in the office.




Q: What are the best binders for Aspergillus, Penicillium, and Citrinin molds?
A: This table is from a 2014 Townsend Letter on Mold and Mycotoxins. I think Neil Nathan was one of the authors.




Q: Is there less toxin exposure when granular forms of herbicides are used on landscapes rather than sprays?
A: Anything that prevents it from getting airborne would help. You still have the issues of contaminating ground water and absorption through the skin if you work the soil afterward or walk barefoot in the area. Not ideal, but better.




Q: Can you review briefly whether mold toxins need to be commonly considered in treating patients living in all climate types, including semi-arid and arid weather regions?
A: It is less likely, but most arid and semi-arid regions are hot, and people have air conditioning. This offers an avenue for mold to enter the house (there is plenty of mold in Las Vegas, but it is nothing like Michigan).




Q: What may be the biological mechanism of substantial multiple food/chemical/odor sensitivities? When the response does NOT look like IgE mediate, but may be within a few minutes to an hour? Thank you.
A: Cell danger response/immune activation leading to autonomic dysfunction. The cell danger response can be set off chronically by infection, a toxin exposure, or emotional stress. Once that is turned on long enough, you get autonomic dysfunction and become hypersensitive to everything. The key is brain plasticity training—DNRS (www.retrainingthebrain or the Gupta Program (www.guptaprogram.com) are the two that I use. Trying to treat with avoidance is too difficult. This tends to work better than desensitization for those types of sensitivities.




Q: Do you see cardiovascular symptoms with mold and mycotoxins, like poor circulation, cold hand and feet, Raynaud syndrome, etc.?
A: Yes—chronic activation of the cell danger response/immune activation will ultimately cause damage to the endothelium and vascular dysfunction. It will also induce autoimmunity in a susceptible individual.




Q: Assuming they could find such a place, would a 2-week test of living somewhere else and feeling better be a reasonable screen for mycotoxicity in patient with suggestive tests who wants more certainty before spending $tens of thousands on remediation?
A: This is true, if you can find that place. I typically send people to live on a beach for two weeks (preferably in the Caribbean). Even though there may be mold, the air circulation with clean (ocean) air takes care of that.




Q: What is a water fast?
A: ? taking nothing but water (no juices or other nutrients). I typically would do this for 3-5 days and only if I think the individual can handle it.




Q: Would you recommend the Mold IgE test for future antibiotic use for chronic individuals?
A: I have never done that. I have no experience




Q: Can you recommend an ozonator for furniture/etc.?
A: There are many. DMRSUP has one for about $100. You need a generator that has a hose that you can use focally on furniture or feed into a box where you have books and the like to be ozonated.




Q: Can UV light kill mold instead of using ozone?
A: UV light will kill mold, but not mold toxins.




Q: Do you advise Glutathione provocation prior Mycotox testing? DMSA prior heavy metal testing?
A: No on the glutathione. For heavy metals, I do a first mornings urine as the unprovoked sample, give 2000mg of DMSA and collect urine for 6 hours for the provoked sample. I then compare the two.




Q: For your workup list, can you please mention how you test for these things? i.e., what lab you like to use.
A: Sorry, this is too general. I use Great Plains for Mycotoxin and OAT testing. Not sure what other labs they are talking about.




Q: How to measure IP flow and NK cells?
A: Any lab can do this. CD3=T cells, CD4=T-helper, CD8=cytotoxic T cells, CD19=B cells, CD16/56=un-activated NK cells, CD57=activated NK cells. Check your local lab for how to order. Cyrex labs also has an much more in depth panel called a lymphocyte MAP.




Q: Does inactivated MSH, as you mentioned with mycotoxins, have anything to do with melanocytes in the skin (i.e., a patient with small patches of vitiligo on shins.... normal thyroid workup)
A: Vitiligo is an autoimmune disorder. A person can be pale if they have chronically low MSH, but it shouldn’t cause vitiligo.




Q: Do you use the nasal culture to test for intranasal fungus, bacteria, and Marcons and how successful do you find the recommended intranasal antibiotics or antifungals?
A: Yes, I use the nasal culture—not the most sensitive for fungus and mold. I use the intranasal sprays—treats most people.




Q: How do you treat the MMP9, C4a, and TGF𝛽?
A: Eliminate the mold exposure, fix the gut and the diet, use binders. These are makers of immune activation—I don’t treat them directly.

IgG Food Allergy Testing: Scientific Evidence of its Validity in Chronic Illness | William Shaw, PhD


Q: Can you please confirm that the patient MUST be eating all the foods in this IgG xMap test for 6 weeks prior to taking the test?
A: I confirm that.




Q: When doing a retest, do you recommend having the person reintroduce prior reactive foods before testing? I've seen patients test low because they avoided a food for 6 months, but when the reintroduce it after retest and have it several times, they react.
A: If a person has a very high value for IgG antibodies against a particular food, immune memory cells store that information. That person should probably never eat those foods again on a regular basis. Retesting is probably useful only for new allergies, not for previous allergies.




Q: Is sheep or buffalo milk also closely related to cow with respect to IgG?
A: Yes, there is considerable similarity among the milk of all these species and likely cross-reactivity.




Q: How much of gluten sensitivity is related to use of round up or other pesticides causing a toxic exposure rather than a direct reaction to gluten containing foods? Some people report ability to tolerate gluten products when they travel abroad.
A: The food map test will not react to glyphosate so any positive is a reaction to the protein sequences of the foods. The failure to react abroad is likely due to elimination of the food at home and reduced immunity. The occasional exposure when traveling is not enough to trigger a reaction.




Q: Is the IgG testing sensitive to food that the patient has not eaten in months to years? How long does the IgG last in the system?
A: See question 2.




Q: Are molds often present in chocolate, like they are in coffee beans?
A: Virtually any food can develop mold, but coffee is a more common source because it the beans are washed (called fermentation) after harvest, making mold growth more common during this washing and subsequent drying.




Q: Do you recommend any special preparation for the test- eating broader variety of foods - 1-2 days prior the testing?
A: Eating foods a day or two before the test is unlikely to affect the test. Basically, the person should be told to keep the same eating habits before the test.




Q: Can mold mediated Congestive heart failure, with Mito damage be resolved?
A: I suspect that most mold damage can be reversed.




Q: Does the Food Map test meat glue and cooked forms of foods?
A: The allergic reaction is mainly due to the sequence of amino acids in the proteins which does not change with cooking. All food protein, cooked or raw, pass through strong acid in the stomach, and a range of digestive enzymes in the stomach and small intestine. It is likely that these factors are much more important than cooking. Great Plains test checks for meat glue.




Q: Foods are altered by digestion. How do your food antigens you use correspond to what the body is seeing?
A: See question 9.




Q: Will this test help clarify how to address intense sensitivities (that do NOT present clinically as allergies) to multiple foods?
A: IgG food allergies do not (usually) cause histamine reactions like IgE allergies but are associated with a large variety of clinical symptoms such as migraine headaches, irritable bowel, depression, psychosis, seizures, autism, attention deficit, and many others.




Q: How is this compared to a different from Cyrex labs testing?
A: Great Plains test covers milk allergies, is covered by some insurance, and can be done on dry blood spots. Cyrex no.




Q: If IgA deficient individuals have frequent eye infections, is that also the case for patients with frequent upper respiratory and GI infections?
A: IgA deficiency likely increases susceptibility to respiratory and GI infections and greatly increases risk of autoimmune diseases.




Q: What would be the next step or test for someone who clearly has symptoms to a particular food but the IgG Food Map is negative or low?
A: Try an elimination of that food and see if symptoms clear up.




Q: Is this food allergy test effected by cans food it packaged in (BPA can linings ) and / or plastic containers?
A: The test only measures reactions to proteins in the food, not additives.




Q: Do you think that A2 milk would be better tolerated by these patients with Autism?
A: Yes.




Q: Do you find that patient's IgG Food Sensitivity panels show elevations of foods they eat often?
A: For the food test to be positive, the person must eat the food often and have an allergic reaction to it. I eat hamburgers almost every other day but do not have an IgG beef allergy.




Q: Does the food sensitivity testing include any dietary guidelines for patients such as hidden sources of the foods and a rotation plan?
A: Great Plains includes a rotation plan with the test. I am not a big fan of rotation diets. I think you should completely eliminate any food that is strongly positive.




Q: Do you have any data on how sensitivities change with a GAPS diet?
A: The GAPS diet will not change food allergies any differently than any other elimination diet.




Q: How long do you recommend someone avoid gluten in an elimination challenge?
A: I think that gluten is such a common element of most diets that most people are not going to adhere to an elimination diet for at least one month. The food allergy test is much more convenient and gives information on all foods, not just gluten.




Q: How do you decide when to rerun the IgG test? how often is it different?
A: See question 2.




Q: Will IgG show in the blood spot if food has been eliminated for an extended period of time (months or years)?
A: No.




Q: What is the clinical usefulness of the IgG C. albicans result as part of the IgG Food MAP?
A: Candida is a common exposure and carbohydrate control is necessary to control Candida which makes it useful when selecting diets.




Q: Do you recommend three days on and three days off or something like that for moderate reaction to food IgG?
A: Each patient will likely have to determine themselves the degree of improvement in an elimination diet and whether the food restriction merits the restriction.




Q: Do you see a reduction in IgG response on repeat IgG food test after decrease in Toxin load in general (removing mycotoxins, metals, etc.)?
A: I have not evaluated such experiments.


Learn new ways to help patients with difficult-to-diagnose and chronic health issues.

The tests discussed throughout each workshop are all used to help identify exposure sources and biochemical imbalances in individuals with chronic health conditions. The Organic Acids Test (OAT) contains multiple markers which may be influenced by environmental and mold toxins. Often, the combination of the OAT, MycoTOX Profile, and GPL-TOX Profile can be used to help identify how a patient might be getting exposed, as well as assist with correlating their symptoms back to these sources. Determining the underlying causes of chronic illnesses for patients is the key to integrative medicine, not just treating the symptoms. The Great Plains Laboratory continues to find new ways to detect these causes of many illnesses and study the correlations between the results and conditions.

Registration includes:

  1. Ability to purchase GPL tests discussed throughout the program at special workshop-only discounted rates.

  2. 60-day access to the full conference recordings.

  3. Permanent PDF access to each speaker’s slides.

  4. The option to purchase continuing education credits (5 credits per day), whether you attend in-person, watch Live Online, or watch the conference recordings at a later date! See detailed information about credits.

  5. An interactive Workshop Hub website where you can live chat and network with attendees and ask questions to the speakers.

  6. And last, but most certainly not least, qualified practitioners will receive a free OAT.

Webinar Q+A: The Toxicity of Trichothecenes - Insights Into This Unique Group of Mycotoxins

On February 16, 2022, The Great Plains Laboratory hosted The Toxicity of Trichothecenes - Insights Into This Unique Group of Mycotoxins webinar with Kurt Woeller, DO. Mycotoxins are toxic compounds produced by many different types of molds. A certain group of mycotoxins called trichothecenes are a large group of chemically related compounds produced by such molds as Fusarium and Stachybotrys. Trichothecenes have some unique toxicity effects, including on cellular production of proteins, DNA synthesis, and more. This lecture explored various mycotoxins within the trichothecene family and some of their related cytotoxicities.

The following Q+A is a grouping of responses from Dr. Woeller’s presentation.


Webinar Attendee Q+A

Q: Is it true that ammonia is an electron donor that degrades the integrity of the epoxide ring?

A: Amines are derived from ammonia and amines can act as nucleophile which attack the epoxide ring - 

 

Q: Dr. Ritchie Shoemaker has deemphasized mycotoxins as a cause of CIRS, saying they are less than 7% of gene activations. He has substituted endotoxins and actinomycetes. Many of his practitioners are saying this doesn't matter, because the structure of these toxins is "all the same.” This has caused them to discount Stachybotrys. Can you address Dr. Shoemakers altered position on toxic mold?

A: I have not dived deeply in Dr. Shoemaker’s claims. From my research, various mycotoxins can be significantly problematic for various reasons through their biological functions. A chemical may have a similar chemical structure on paper, but even subtle differences based on changing functional groups, positions of these groups on the molecule which can alter the chemicals orbital configurations, etc. are sometimes enough to change its cellular reactivity. 

 

Q: Do the same things occur in the body when these are inhaled vs being absorbed in the GI or skin? 

A: Yes, from my research and understanding. Now, there certainly could be some differences in specific cellular responses within the gut versus the skin, but when these toxins find their way into the lymphatic system, and eventually the bloodstream their distribution throughout the body to other organ systems should be the same.

 

Q: Which probiotics are low in histamine? 

A: Here is the link from presentation. This article is a good place to start your research.

 

Q: I am curious of your thoughts on the carnivore diet for patients?

A: I have not looked into this.

 

Q: What does PQQ mean?

A: Pyrroloquinoline Quinone – stimulates mitogenesis


The material contained within this article and webinar is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.



Kurt Woeller, DO

FOUNDER OF INTEGRATIVE MEDICINE ACADEMY
Kurt N. Woeller, DO, has been an integrative medicine physician and biomedical Autism specialist for over 20+ years. He is an author of several health books including Autism – The Road To Recovery, Methyl-B12 Therapy For Autism, Methyl-B12 for Alzheimer’s Disease and Dementia, and 5 Things You MUST Do Right Now To Help With Your Rheumatoid Arthritis. He is an international speaker, educator, and practicing clinician offering specialized interventions for individuals with complex medical conditions. His health consulting practice for Autism alone is multinational with families from various countries. Dr. Woeller serves as a clinical and lab consult for Functional Medicine Clinical Rounds, as well as provides educational seminars for Great Plains Laboratory. He is co-founder of Integrative Medicine Academy (www.IntegrativeMedicineAcademy.com), which is an online training academy for health practitioners learning integrative medicine.

Webinar Q+A: Mycotoxin Induced Mitochondrial Dysfunction And Cytotoxicity

On December 15, 2021, The Great Plains Laboratory hosted the Mycotoxin Induced Mitochondrial Dysfunction and Cytotoxicity webinar with Kurt Woeller, DO. Various mycotoxins can have significant adverse effects with regard to cellular function. Through DNA and RNA disruption and/or induction of oxidative stress mycotoxins can lead to various diseases, including cancer. A major target of intracellular mycotoxins are the mitochondria. This lecture by Dr. Kurt Woeller discussed some of the cytotoxic effects of mycotoxins on mitochondrial function.

The following Q+A is a grouping of responses from Dr. Woeller’s presentation.


Mycotoxin Induced Mitochondrial Dysfunction And Cytotoxicity Q+A

Q: Is it recommended for all patients who have mycotoxins to have some form of multivitamin therapy since vitamins have a huge impact on the ECT cycle?

A: I think so. I have most everyone on foundational supplements such as a multivitamin.

Q: If you have mold and candida, do you deal with them both simultaneously, or which do you treat first generally?

A: Depends on the severity of the condition, but in general mold because it can make candida worse.

Q: Maple Syrup Urine Disease is a genetic disorder in which a person is unable to break down the branched-chain amino acids. Would riboflavin make a difference in this disorder?

A: Great question and I do not know. It probably might help some.

Q: Is any other way to measure ochratoxin than the Organic Acids Test?

A: Ochratoxin is measured on the MycoTOX Profile from GPL. The OAT does not measure Ochratoxin or any other mycotoxins.

Q: Please indicate treatment strategies for aspergillus mold exposure and mycotoxins for patients with respiratory rx MAST CIRS.

A: This is a very in-depth topic and there are some webinars on the GPL site that address this, as well as seminars that are put on via the GPL Academy.

Q: I had a patient who was higher in gliotoxin than that, and we were able to completely eliminate it in less than 9 days using Ascorbic Acid and Ascorbates. We repeated this several times and got the same results using testing immediately before and immediately after the use of IV-Vitamin C. The whole process took about 9 or 10 days.

A: Awesome. I do see the value in ascorbic acid intervention too.

The material contained within this article and webinar is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.



Kurt Woeller, DO

FOUNDER OF INTEGRATIVE MEDICINE ACADEMY
Kurt N. Woeller, DO, has been an integrative medicine physician and biomedical Autism specialist for over 20+ years. He is an author of several health books including Autism – The Road To Recovery, Methyl-B12 Therapy For Autism, Methyl-B12 for Alzheimer’s Disease and Dementia, and 5 Things You MUST Do Right Now To Help With Your Rheumatoid Arthritis. He is an international speaker, educator, and practicing clinician offering specialized interventions for individuals with complex medical conditions. His health consulting practice for Autism alone is multinational with families from various countries. Dr. Woeller serves as a clinical and lab consult for Functional Medicine Clinical Rounds, as well as provides educational seminars for Great Plains Laboratory. He is co-founder of Integrative Medicine Academy (www.IntegrativeMedicineAcademy.com), which is an online training academy for health practitioners learning integrative medicine.

IgG Food Allergy and Mycotoxin Testing with William Shaw, PhD

On November 12-14, 2021, GPL Academy hosted the Environmental Toxin Summit in San Diego, CA as well as streamed online simultaneously. This three-day event focused on the epidemics of toxin exposure, including both toxic chemicals in our environment and mycotoxins from mold. These toxins can cause symptoms of many acute and chronic health disorders. Those who attended the summit learned how to use effective diagnostic and treatment protocols for their patients with toxin exposure and get them on the road to recovery.

The following Q+A is a grouping of responses from Dr. Shaw’s presentations.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


William Shaw, PhD

LAB DIRECTOR AT THE GREAT PLAINS LABORATORY, LLC
William Shaw, PhD, is board certified in the fields of clinical chemistry and toxicology by the American Board of Clinical Chemistry. Before he founded The Great Plains Laboratory, LLC, Dr. Shaw worked for the Centers for Disease Control and Prevention (CDC), Children's Mercy Hospital, University of Missouri at Kansas City School of Medicine, and Smith Kline Laboratories. He is the author of Biological Treatments for Autism and PDD, originally published in 1998 and Autism: Beyond the Basics, published in 2009. He is also a frequent speaker at conferences worldwide.

IgG Food Allergy Testing: Scientific Evidence
of its Validity in Chronic Illness

Q: How do you interpret this test in those with total serum IgG4? No value in running it?

A: The IgG Food MAP evaluates IgG1-4, not just IgG4, and is therefore going to provide more detailed information. Exclusively running IgG4 is not ideal since it has a lower (~6%) representation of the IgGs overall, and it has a reduced ability to induce complement and cell activation.

Q: Do you happen to know if there is a difference in raw milk versus conventional milk in the IgG testing?

A: The IgG test is utilizing the protein from dairy milk, but does not differentiate between raw milk and pasteurized milk.

Q: Regarding food allergies- I have been taught that in patients with leaky gut, then of course their "usual" foods will show as allergens because that's what's in there and are the proteins that leak into the blood the most. So, is it elimination diet that's the most helpful or healing the gut lining? Or a combination of both?

A: Depends on the cause of the leaky gut. In general, reducing the inflammatory foods while the cause is being identified/treated is useful. This can be done by the elimination diet, but the elimination diet can be very restrictive in nature and cumbersome for a lot of patients. The IgG Food Allergy is a short cut to identifying the foods that are causing inflammation without having to remove unnecessary foods, making it easier for the patient.

Q: How does fasting affect IGG?

A: IgG’s are the immunoglobins with the longest half-life (~33 days), and therefore a fasted state should not influence the results.

Q: Cyrex labs say their food allergy testing evaluates cooked and raw food as we don't eat everything raw, and we eat some in cooked form. Does Great Plains also factor this in their tests? Is the difference in type important?

A: GPL evaluates various forms of the proteins in the foods (e.g. Cows’ and goats’ milk, casein, whey, beta-lactoglobulin, sheep’s yogurt, yogurt, mozzarella and cheddar cheese) to account for the changes in epitopes, which can occur during food processing. Remember that any protein, cooked or raw, undergoes exposure to concentrated acid and the enzyme pepsin in the stomach and then extensive exposure to other digestive enzymes in the small intestine. These alterations are much more profound than whether a protein is cooked or raw. Cooking does not change the amino acid sequence of a food while acid and digestive enzymes cause pronounced changes in amino acid sequences of food.

Q: How effective is the IgG Food map on a patient being treated with Humira? And on Xolair?

A: The IgG response of those individuals on the immune modulators may not be favorable for this testing. Humira targets and blocks TNF-alpha, which could potentially reduce the IgG response. Xolair may also because though it inhibits the binding of IgE, it also influences FcεRI receptors on basophils, potentially reducing the IgG’s reactivity.

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Organic Acids and Mycotoxins: Correlations
With Mold in Various Chronic Illnesses

Q: What would you do with pregnant women with mycotoxins? Would you detox them or wait until pregnancy is over?

A: I would advise the woman to move out of the contaminated space immediately. I wouldn’t advise active detox while pregnant as you may increase transference to the fetus.

Q: If glutathione is the issue with provocation, are there other products that may increase the probability of an accurate test? Heat, NAC, use of binders etc. These are so tissue bound I have seen negative tests become extremely positive 3 months later with the use of recommended detox.

A: The test was developed without use of any provocation methods. If you choose to do anything a warm bath/shower or sauna the night before may encourage more toxin into the urine.

Q: For a patient with chronic and relapsing cocci infection for years, would you have a high suspicion of mycotoxicity? Would daily use of itraconazole for over a year affect urine MycoTOX test?

A: It may be in the differential for things to consider. Itraconazole can reduce toxins on the MycoTOX Profile if the mold exposure is eliminated. I would suspect that most mycotoxins would be negative or low after a year of itraconazole if the source of mold in the house has been eliminated.

Q: Do you have a mold treatment protocol vs Shoemaker protocol?

A: Check out New Beginnings Nutritionals’ mold protocol.

Q: I've seen patients with histamine intolerance and mold colonization have reactions when taking binders, particularly GI Detox or another combination binder. Is this something you've experienced? What would be a good binder or something else to consider first for these sensitive individuals?

A: This is common. Slower administration of binders or use of single agents before a combo product is a strategy to consider. For very sensitive patients allow for reduction in aggravation before addition of next dose, even if that means waiting a few days for the client to feel able to handle another dose.

Q: What testing can be done to determine Mycotoxins in the sinuses? What is the best way to remove Mycotoxins from the sinuses? Is there going to be information about treating sinuses directly in conjunction with the other treatments? Do you have any pearls? What is an example of a nasal anti-fungal inhaler- product and dosage and duration?

A: Urine mycotoxin testing looks at mycotoxins that circulate in the blood stream (all over the body, including the sinus). If you want to know about mold growth in the sinus look at nasal symptoms or consider a nasal swab and culture. For removing mycotoxins you use detox factors like binders and glutathione. For mold removal direct nasal sprays are recommended. Prescription and natural options are available. Consider nasal GSE

Q: Does nano zeolite clinoptilote just bind metals or can it be used with mycotoxins?

A: It can bind to mycotoxins

Q: Can you please give us doses of Binder for infants and children?

A: Dose depends on the binder. Low and slow is always a good strategy. It should not be given more than once a day.

Q: Does a mold colonization on the OAT test need to be treated if the MycoTOX Profile is within reference range?

A: Yes. A colonization can still produce mycotoxins at a low, consistent level. Mold itself has harmful effects, like those of yeast.

Q: Do mold infestations in GI tract produce biofilm? If so, are antifungals always successful in breaking down the biofilm barrier?

A: Biofilms can be produced. Herbal antifungals usually have biofilm disruption properties. Prescriptions may not have this capability. Antifungal with biofilm disruption properties can be successful. Always, is a loaded word and I cannot guarantee it will always be effective.

Q: What is the best anti-fungal treatment regimen for candida?

A: Common antimicrobial herbs can be used to treat candida like garlic, ginger, berberine, etc. there is no one size fits all. Nystatin or Diflucan are also options.

Q: I have a patient with high fungal markers on OAT, but his mycotoxins had only a slight elevation in ochratoxin. Please advise.

A: A colonization can still produce mycotoxins at a low, consistent level. Mold itself has harmful effects, like those of yeast. The person is most likely not currently exposed to water damage.

Q: How many days prior to taking the OAT test should we be fasting from medications or supplements that could mask correct OAT results?

A: You only need to fast from the listed foods/supplements. Others can be discontinued if you would like for your own interpretation purposes. A good time frame is 1 week if this is possible for the patient.

Q: Please comment on treatment for Chaetoglobosin A, particularly when both the house and the office where the patient lives were found negative?

A: Treatment for this toxin is like others. You would need to remove the source and detox the toxins. Binders like charcoal bind all mycotoxins at some level and can be effective for this toxin too. Consider a combo binder product. I suspect that the house and office mold testing are likely giving false negative results.

Q: What botanicals do you use to treat SIBo?

A: Common antimicrobial herbs can be used to treat SIBO like garlic, ginger, berberine, etc.

Q: The notes indicate that oxalates are produced by molds like aspergillus and penicillium. Does Chaetoglobosin A also produce oxalates?

A: Chaetoglobosin A is a toxin therefore doesn’t produce anything. Chaetomium mold, which produces chaetoglobosin a, hasn’t yet been shown to produce oxalates.

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Non-Metal Toxic Chemicals and Their Effects
on Health: Glyphosate and Beyond

Q: Do any of the GPL-Tox values extrapolate polyethylene glycol or polysorbate? Will it be added?

A: Both Polyethylene glycol (PEG) and polysorbate utilize ethylene oxide in the manufacturing process, which is measured on the GPL-Tox Profile; marker number 9.

Q: It was mentioned pine wood is not ideal for a sauna <link sauna to https://www.greatplainslaboratory.com/gpl-blog-source/2016/12/12/how-to-maximize-the-benefits-of-sauna-for-detoxification?rq=sauna>, but a lot of saunas are made with pine wood. Does pine wood inhibit the effects of detoxification? Can you explain further?

A: The resin that pine contains has certain alkaloids, and other nitrogen containing organic compounds, that can be toxic when released with excessive heat.

Q: Can lower toxin levels be significant in those with neurologic compromise? Immune suppression? mycotoxin load etc.?

A: Statistically speaking, above the 95th percentile is the most significant. There are always the outliers who are extremely chemically sensitive, or have multiple comorbidities to which they have overfilled their bucket so to speak, who will react to lower values.

Q: Have you seen any increase in toxins with kids using slime, which uses glue as a base?

A: Not directly.

Q: Can you comment on brevatoxins and red tide? Testing treatment binder types?

A: We are not currently measuring these toxins, but plan to add them in the future. However, the general detoxification method utilized for the other environmental toxins would likely help with the elimination of these toxins, theoretically.

Q: What is your recommendation to detox from glyphosate in addition to removing the source? There are multiple protocols out there. Do you have a favorite?

A: The most important detox method is to switch to organic foods. This step is 10 times more important than other detox methods although Chlorella, sauna, and humic and fulvic acids, have also been recommended.

Q: Does Sauna and liposomal glutathione eliminate glyphosate?"

A: Sauna may help but I know of no evidence that glutathione is effective. Switching to an organic diet is the single most important therapy.

Q: What's best type of sauna (Infrared, near-infrared or far-infrared)? Would you suggest a particular brand for in-home use?

A: IR is the preferred due to its ability to increase the internal temperature without excessive heat. It is generally a good option for patients who are heat sensitive.

Sunlighten has a very good reputation.

Q: Are hyperbaric chambers any help in removing molds and toxic chemicals?

A: Hyperbaric chambers can be helpful in the elimination of the mycotoxins and toxic chemicals by increasing oxidative detox reactions.

Q: Can you explain the difference between NAC and Cysteine and whether Cysteine may be a good substitute if NAC not available?

A: N-Acetylcysteine as compared to L-cysteine (the supplemental form of cysteine derived mainly from swine hair or poultry feathers) has the acetyl group attached to the nitrogen, making it more water soluble, increases the absorption and distribution, as well as reduces the thiol reactivity making it less susceptible to oxidation.

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Functional Medicine Answers with Kurt Woeller, DO

On November 12-14, 2021, GPL Academy hosted the Environmental Toxin Summit in San Diego, CA as well as streamed online simultaneously. This three-day event focused on the epidemics of toxin exposure, including both toxic chemicals in our environment and mycotoxins from mold. These toxins can cause symptoms of many acute and chronic health disorders. Those who attended the summit learned how to use effective diagnostic and treatment protocols for their patients with toxin exposure and get them on the road to recovery.

The following Q+A is a grouping of responses from Dr. Woeller’s presentations.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


Kurt Woeller, DO

FOUNDER OF INTEGRATIVE MEDICINE ACADEMY
Kurt N. Woeller, DO has been an integrative medicine physician and biomedical autism specialist for over 20+ years. He is an author of several health books including Autism – The Road To Recovery, Methyl-B12 Therapy For Autism, Methyl-B12 for Alzheimer’s Disease and Dementia, and 5 Things You MUST Do Right Now To Help With Your Rheumatoid Arthritis. He is an international speaker, educator, and practicing clinician offering specialized interventions for individuals with complex medical conditions. His health consulting practice for autism alone is multinational with families from various countries. Dr. Woeller serves as a clinical and lab consult for Functional Medicine Clinical Rounds, as well as provides educational seminars for Great Plains Laboratory, LLC. He is co-founder of Integrative Medicine Academy, which is an online training academy for health practitioners learning integrative medicine.

Q: If you have been supplementing with Lithium orotate 10mg and the hair test comes back HIGH do you back down, stop, or just continue at the same dose? The child has high Glutamate marker on Neurotransmitter test.

A: I would personally back down to the 4.8 mg dose and retest again in 90 days, particularly if there have been some positive changes. If there is no significant change, then I would likely just discontinue the supplement.

Q: Based on various research studies, it has been shown Biocidin can treat primary hyperhidrosis. Would you recommend long-term daily Biocidin dosing or implementation of a cyclic protocol over a shortened period?

A: For this, I would recommend a long-term daily dosing versus cyclical dosing.

Q: Why did you choose Biocidin capsules vs drops?

A: I do not remember the specifics for that particular case. Usually, it comes down to taste sensitivity of a child versus their ability to swallow capsules.

Q: Did you increase the dose slowly?

A: No.

Q: Was there a die-off at full dose?

A: It did not happen in that case, but that is a possibility. Therefore, starting at a lower dose is okay to do if you get the sense die-off could happen.

Q: How did you choose Flagyl dose of 250 mg tid for the 2-year-old?

A: The medications were being handled by another physician since the child lived in another state. It was a higher dose for sure with the child having already been through multiple other treatments up to that point that were unsuccessful.

Q: I am a bit unclear but is it ok to continue Vit C with high oxalates?

A: This is a controversial situation, and it is not clear cut in every situation. There are quite a few studies and reference websites for kidney stone sufferers that describe up to 2000mg daily oral of Vitamin C to be okay. Therefore, in my experience modest dosing of ascorbic acid, e.g., 250mg to 500mg daily has been fine. I have even gone to 2000mg daily and not seen any problems. However, in most situations, I keep the dosing to less than 500mg daily but do not stop it entirely.

Q: What cholesterol triggers your concern as I find iCNS issues with 120 -135? Is it a variable number depending on the severity of the CNS presentation?

A: Yes. I have seen people who have a total cholesterol of 120 (or lower) and seem fine. In others that value is problematic for them.

Q: Can you augment a 165?

A: At this level I would not be supplementing with Sonic Cholesterol.

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Considerations And Protocols For The Complex Patient With James Neuenschwander, MD & Elena Villanueva, DC (Copy)

The Great Plains Laboratory has been educating practitioners for over 15 years on how to help patients heal through cutting-edge testing, research and protocols. In our recent 2-Day OAT+TOX Workshop, speakers focused on the epidemic of environmental toxin exposure, from the many chemicals we encounter every day to mycotoxins released from mold. Attendees learned about many common environmental pollutants from the 173 chemicals tested by the GPL-TOX Profile.

The following Q+A is a grouping of responses from a distinguished pool of speakers who participated in the OAT+TOX Workshop with his own unique topics and lectures as labeled.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


James Neuenschwander, MD

A graduate of the University of Michigan with both a Bachelor of Science degree in Molecular and Cellular Biology as well as a MD degree. Dr. Neu (as he is also known) is dually board certified in both Emergency and Integrative Medicine and has been the owner of the Bio Energy Medical Center since its opening in 1988.

Q: What cutoff is ‘Lots” on an ERMI? 

A: I typically start paying attention if the number is over 2; but in my state (Michigan), many houses are over 2. The ERMI score also does not take into account how moldy the house is in general, only the difference between toxin producing mold and non-toxin producing mold. I will use the mold numbers to calculate a HERSMI Score.  If it is over 16, the house is a problem. 12-16 might be a problem if the person is sensitive.

Q: Can mycotoxins cause a progressive pulmonary fibrosis?

A: I think that anything that causes consistent immune activation (like mold toxins) can cause pulmonary fibrosis.

Q: How about triphala? Ayurvedic herb that helps with constipation and detoxifier, antioxidant and more.. 

A: I frequently use Triphala to help with constipation. I don’t use is it as a detoxifier/antioxidant/etc—I think there are better options for that.

Q: Are you familiar with phenomenal AIRE? It produces ions? Is this ozone?

A: It is not ozone, but it incidentally generates ozone from room air. The idea behind an ionizer is to charge particles so they stick to each other and surfaces. The energy needed to create the ions can also create ozone from the oxygen in the air. I am not a fan.

It is said to join particles to bond together known as agglomeration.

Q: What are your thoughts regarding treating mold with thermal fogging with a solution like BioBalance vs. treating with ozone generator? 

A: I think ozonation is probably the most effective way of treating mold after you have removed the obvious contamination (this won’t get mold off of wood joists or rafters because it won’t penetrate the wood deeply enough) with other techniques. This requires that people are out of the building and requires an industrial strength, whole house ozonator.

Q: In a patient with Gilbert’s, what precautions are needed?

A: The issue with Gilbert’s is that they will be more susceptible to certain environmental toxins. Supporting glutathione (NAC, ALA, liposomal glutathione supplements, Setria) can help with glucuronidation (the problem with Gilbert’s).

Q: I also live in Michigan. What water filter do you find works well with our water?

A: Every water system will have different issues. I am on a well. I have completely different issues than someone that is on Detroit City water. I use the Zero Water filter—this is a pour through, multi-stage system that removes almost everything. My biggest problem is iron and bacteria—not any issues with other water supplies. This system will also remove chlorine and fluoride and heavy metals. Most of the time, a combination charcoal/reverse osmosis water filtration system works for most things, but does not remove all the thyroid.

Q: Can you just take ox bile with binders so patients have more time flexibility?  Some must take meds before eating.

A: Yes. You can take them together.

Q: Patients with severe MCS that have such a hard time taking ANY med/supplement...where do you start with mold or mycotoxin treatment? Slow small amounts of binder until tolerating?

A: First, I will start with supportive supplements (like vitamin C) before I start with detox supplements. Then, I will start with a single binder (not a combination) at low dose and work my way up. Many of the symptoms MCS patients have are related to histamine, so I also tend to start with things like luteolin (and quercetin if they are not sensitive to salicylate).

Q: Is Cholestyramine constipating?

A: It is almost always constipating. I always start something (like magnesium citrate or sodium ascorbate) to help with the constipation.

Q: Do you have any protocols for people to detox from the CV injections and their injuries?

A: I assume you are referring to the COVID vaccines—check out the FLCCC.org website. They have a protocol for long-haul COVID. It works for most vaccine injuries. Above and beyond that, it requires someone familiar with detox from vaccine injuries—that is an entire workshop, not a simple answer.

Q: It’s been shown that DMSA, etc. provoking sends toxins all of the body, into joints, etc. Do you see this?

A: Not really. DMSA will bind metals in tissues. Because it is a sulfur bond, it is not easily reversible. The metal can be displaced by another metal with a higher affinity, so you can have some distribution. I also give DMSA according to the Cutler protocol—every three hours for three days every two weeks. I also make sure that patients have adequate glutathione and that they don’t have intestinal yeast. There is no way to remove metals without some distribution, but that is better (when managed properly) than leaving the metals in the body.

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Elena Villanueva, DC

Elena Villanueva is an internationally recognized health coach and crusader for ending the global mental health crisis and educating the public and other health professionals that mental health conditions are actually ‘brain health’ issues and when the underlying causes are found, the brain health conditions can be reversed.

Q: Do you have a toxic exposure history form that you like?

A: The questions we ask in this area of our intake include the following. We also ask if they have any history of these exposures from their past.

Q: Would you be willing to share your symptom sheet and what you are utilizing for these patients to track symptoms?

A: Thank you for asking! Great question! We offer this and much more for our practitioners who go through our MHH certification program.

Q: What home mold testing do you recommend?

A: Home testing kits are not effective. We recommend our clients find a local mold testing company in their area to come out and test the house for mold. The price, depending on the state can range between $600-$800 for the testing and report.

Q: What do you use to break up the biofilm?

A: There are many different substances that can break up biofilm. The humic/fulvic compounds (like the ones found in the Cellcore product lines are effective at breaking up biofilm.  

Biofilm X and Interphase are also great biofilm busters, as are coffee enemas, and Biocidin also breaks up biofilm. Keep in mind that biofilm, depending on how dense and how much build-up there is, can take as little as 8 weeks to as long as 8 months to fully break up and come out. I am basing this comment on our experience with our clients.

Q: Are you giving biofilm disrupters alongside the binders in your patients that had new molds show up in later tests, or do you think just using binders alone was lowering the load enough to allow the body to break up the biofilm on its own?

A: The protocols we put them on do break up biofilm, so it’s not common that we need to add something extra like Interphase or some added additional biofilm buster.

Q: Is the “chemical toxin” test the GPL-TOX?

A: Yes.

Q: I do see a lot of sick patients that have high B12 lab readings.  What are your thoughts on that?

A: Such a great question! They could be showing high levels of blood serum B12 or urinary metabolite patterns of high B12 for the following reasons:

  1. They are taking B12 currently.

  2. They have specific genetic methylation SNPS (MTRR A66G) that may be ‘mal expressing’ where they are not able to uptake the B12 into the cell … so they may show ‘high’ levels in blood serum or in urine, but are actually cellularly ‘deficient’ - in these cases either a sublingual or transdermal delivery method for methylated B12 is going to be the ideal delivery method for cellular uptake.

Q: Can you comment on when you choose Liposomal Glutathione vs N acetylcysteine for detox?

A: There are definitely varying opinions on this one. We actually use BOTH, glutathione, and NAC. Previously, a few years ago, we were using glutathione and saw marked improvements in homocysteine, CRP, and MCV numbers, which can indicate methylation issues, which can cause inefficiency of phase 1 AND 2  detox pathways, leading to excessive inflammation (of course we also had clients on methyl folate/methyl B12 as well, per their genetics -- to make sure phase 1 and 2 Detox pathways were optimized). In the last year or so we have added NAC as well.

Q: I am interested in what exactly she is using for kidney/liver detox

A: We vary what we use from LVGB by DFH, to SP products, to Cellcore liver gallbladder support. There are many different brands that all work well.

Q: do you add in digestives like bile or HCL etc for support?

A: When we see it’s needed, yes we do.  We definitely do when we are doing specific gut repair (after removing the toxins and confirming with labs) It’s a fine line when we are not wanting to overload the client with supplements. We want them to be able to take the least amount of supplements with the greatest effect. Too many supplements make the clients/patients feel overwhelmed and often they lose compliance.

Q: Please expand on biofilm treatment protocol… list options and when to use in the overall treatment protocol.

A: Discussed biofilm in the above questions.

Q: What is TUDCA and what is inside Para 1;2;3

A: Tudca provides liver/gallbladder support. You can go to HERE to see the labels on the Para’s.

Q: Do you see 3-4 week cough as a herx symptom?

A: I would ask more questions and get a deeper history on this. The client/patient may be having an IgG type of inflammatory reaction to an ingredient in one of the supplements that is causing the cough. Or it could be a recent food they recently started eating. More times than not, a herx is more ‘severe’ symptom wise, than a cough. So definitely ask more questions. You could also do an ‘elimination’ test by having them stop all supplements to see if the cough goes away, and then one at a time every 5 days or so, start adding in one more of the supplements on their list…. and record if sx comes back with one of the supplements.

Q: …But you are putting them on new supplements.  So how do you tell the difference between a reaction and a herx?

A: It’s not as common to have a true ‘reaction’ to food/herb/nutraceutical based protocols. More than likely the sx are because the client is detoxing which can lead to mild sx or more severe ones (herx). If you are suspecting a true reaction, talk to the patient/client to get a history … they usually are already aware of their allergies to certain things. Use your discernment and if needed, take them off all supplements and slowly have them add one in at a time, sometimes micro dosing them with each supplement even. You’ll learn with experience!

Lyme, Mold, Mycotoxins & Testing Answers with Jasmyne Brown, ND, Darin Ingels, ND & More!

On November 12-14, 2021, GPL Academy hosted the Environmental Toxin Summit in San Diego, CA as well as streamed online simultaneously. This three-day event focused on the epidemics of toxin exposure, including both toxic chemicals in our environment and mycotoxins from mold. These toxins can cause symptoms of many acute and chronic health disorders. Those who attended the summit learned how to use effective diagnostic and treatment protocols for their patients with toxin exposure and get them on the road to recovery.

The following Q+A is a grouping of responses from a distinguished pool of speakers who participated in the Environmental Toxin Summit with their own unique topics and lectures as labeled.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


Jasmyne Brown, ND

Jasmyne Brown is a board-certified and licensed naturopathic doctor. She earned her Bachelor of Science in chemistry with a minor in biology from Alabama Agricultural and Mechanical University in 2013. Then she earned her Doctor of Naturopathic Medicine and Master of Human Nutrition degrees from the University of Bridgeport College of Naturopathic Medicine in 2017. Her professional training allows her to be able to interpret the GPL lab tests in a clinical manner, plus she enjoys identifying the biochemical pathways within our bodies and how nutrition and lifestyle impact them.

The Clinical Approach of a GPL Consultant
on GPL Testing

Q: Please comment about Chaetoglobosin A and appropriate treatment protocols?

A: Treatment for this toxin is like others. You would need to remove the source and detox the toxins. Binders like charcoal bind all mycotoxins at some level and can be effective for this toxin too. Consider a combo binder product.

Q: If zearalenone is very elevated (90) but the patient has low estrogen, would you believe the results?

A: Yes. Zearalenone does not necessarily increase your own estrogen but has its own estrogenic effects. Also, the LC/MS is specific to the toxins so if it’s populating there is an exposure. Also realize all toxins do not cause the same symptoms in every person.

What would be a good next step if you have a sensitive patient with mold who reacts poorly to binders such as GI Detox? Is there a binder that works better for sensitive individuals or something that needs to be done first?

A: You can use another product that doesn’t contain strong binders like charcoal and clay. Consider ToxinPul™ Multi-Function Detox by New Beginnings Nutritional’s.

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Darin Ingels, ND

Dr. Ingels is a licensed naturopathic doctor with more than 30 years of experience in the healthcare field. He is a Fellow of the American Academy of Environmental Medicine and has been published extensively. Dr. Ingels is the author of “The Lyme Solution: A 5-Part Plan to Fight the Inflammatory Autoimmune Response and Beat Lyme Disease”, a comprehensive natural approach to treating Lyme disease. Dr. Ingels specializes in Lyme disease, MS, mold/mycotoxins, and chronic immune dysfunction. He uses diet, nutrients, herbs, homeopathy, and immunotherapy to help his patients achieve better health.

Lyme, Mold and Mycotoxins: Strategies For Navigating Complex Illness

Q: What's the dosing of TRISALTS for Herx?

A: Take 1 tsp every 2-3 hours until feeling better. May cause loose stools at higher doses, so warn patients.

Q: If you are exposed to mycotoxins at the office, do you carry a risk of bringing the toxin home through your clothes and belongings?

A: It is possible that porous material can contaminate other objects, so if the exposure at work were high enough and gets in your clothes when you sit on a chair, or bed it is possible to contaminate those surfaces. However, this is not likely the way most people get exposure, and it seems this contributes to a minimal form of exposure.

Q: For treatment of molds/mycotoxins, do you treat with antifungal medication (Diflucan, Nystatin) concurrent with binders?

A: If you are treating actual mold colonization, you need itraconazole as other azoles are not effective at killing mold. They are good for yeast, but not for mold. Yes, I use concurrent with binders as they are doing different things in the body.

Q: If you use binder products from CellCore Biosciences, does that mean you do not need to use Cholestyramin or Welchol?

A: Generally speaking, yes. You do not necessarily need to have multiple binders on board. Just monitor your patient’s progress and make sure their mycotoxin levels are dropping.

Q: One of my patients decided to try this ionic foot bath instead of the IonCleanse: Regain Health & Vitality ionic foot cleanse. Are you familiar with this version and do you think it will work? She purchased it since it costs less than $200.

A: I can’t speak to other ion foot baths but know that IonCleanse has a patent on their device, so it is unlike other ion generators out there. My personal experience with IonCleanse from AMD is that most people have a good response to it. I have had other patients get different devices and they do not seem to work as well, so I’m betting you get what you pay for.

Q: Could celiac symptoms be from contamination of the wheat with mold/toxins? Instead of allergy?

A: Not likely as Celiac disease is a genetic disorder in breaking gliadin down. No doubt, mycotoxin and mold contamination can aggravate both Celiac and non-celiac gluten enteropathy.


Mark Su, MD

Mark Su is a board-certified family physician of 18 years, practicing in Newburyport, MA. He founded Personal Care Physicians as a functional medicine practice in 2014, where he and 4 other clinicians provide both primary care as well as consultation services for chronic complex illness patients. As such, he's been evaluating and treating patients for mold and other related conditions across a variety of symptom and severity stages, creating a rather diverse experience beyond treating only severely dysfunctionally ill patients. He is currently the vice president of ISEAI, and also a member of the IFM and ILADS, among other organizations.

EnvironmnetAl Illnesses
and treatment Protocols

Q: B/W salicylate, oxalate and histamine/MCAS issues, what to test for/address first?

A: I view all 3 of these matters as "back 9", or secondary, root cause problems. Commonly, there are deeper, primary root cause problems causing each of these, so I'd look for those root causes. Reflective of the very essence of my presentation, one is not likely to find a singular cause - I believe it would be very, very rare for a practitioner to cast a wide enough net and yield only one cause for any or all of these problems. But at this point in time, if I was forced to name one most likely cause, or name the one cause that is likely to be having the greatest contribution to these issues (among the many found), I'd suspect it to be mycotoxins. That's likely to be the case with histamine/MCAS, certainly, with high oxalates a close second (commonly because where there are mycotoxins, yeast is likely to be a problem as well, and oxalates are common with the latter). With high salicylate levels, if we're talking about the marker under the "toxin" biomarkers within the GPL OAT results, my suspicion would more likely lie within a gut dysbiosis root cause, but even that is commonly going to be associated with mycotoxin illness. Whereas, any other exposome/"non-self" condition (incl. tickborne illnesses, heavy metals, viruses, etc) or other "self" condition (incl. immune deficiencies, hormone imbalances, methylation dysfunctions, etc) is not nearly as likely to (singularly) cause these problems.... A decent second suspicion would be to look at gut health, which is arguably unfair in comparison since it is a more categorical answer than mycotoxins being a more focal/singular response - gut health could include bacterial dysbiosis that is driving salicylate marker abnormalities; genetic-based deficiencies in histamine metabolism (leading to excess histamine in the gut); and/or fungal dysbiosis leading to high oxalates.

Q: What are the best way to lower oxalate levels?

A: Look for root causes. Dr. Woeller/GPL staff often teach that 3 of the most common causes are yeast, oxalate rich foods, and B6 deficiency. In my experience, yeast, as reflected by high arabinose levels (marker 7 on the OAT), is a common problem, even in a more generalized health population (vs. the chronic, complex illness patients). Given such, and my clinical impression that not many patients, as a generalized population, are likely to be eating a large enough amount of oxalate foods, yeast is likely to be the most common culprit among these three. (B6 deficiency, on some level, may be pretty common, but my suspicion is that this isn't likely to be a strong enough deficiency in most people to cause high oxalates - again, across the generalized population).

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Emily Givler, DSC

Emily Givler is a Functional/Genetic Nutrition Consultant, researcher, and lecturer with a thriving clinical practice at Tree of Life Health in Lancaster County, Pennsylvania. She holds advanced degrees and certifications in Nutrition, Herbalism, and Nutrigenomics from the Holt Institute of Medicine, PanAmerican University of Natural Health, and Functional Genomic Analysis where she now serves as an adviser and supplement formulator. In her practice, Ms. Givler utilizes personalized dietary and nutritional protocols based on genetic predispositions, environmental and epigenetic influences, and functional lab testing to help her clients regain their health.

Oxalates and Mold: A Hidden Source
of Inflammation

Q: What about stone dissolving herbal therapy?

A: There are several herbal preparations that may be beneficial for high oxalate individuals. This paper, Dietary Plants for the Prevention and Management of Kidney Stones: Preclinical and Clinical Evidence and Molecular Mechanisms, summarizes their potential benefits and specific mechanisms.

Q: Do you see a pattern of lactose intolerance in genetic testing with patients with high oxalates?

A: Not necessarily, though lactose intolerance can be an exacerbating factor. Far more people will be lactose intolerant than will have a problem with oxalates.

Q: Do you have a protocol for oxalate that you can share with us?

A: The first step would be to assess which mechanisms for over absorbed oxalates are coming into play. Next, we would add Epsom salt soaks, working progressively up to 20 min 3-5x/week as tolerated. Evaluate the diet for volume of oxalates and start reducing/binding oxalates at roughly 10% per week. The next steps depend on the individual presentation and may be bile support, probiotics, antimicrobials, B1, and/or B6. The individual presentation will typically dictate the order and necessity of those pieces.

Q: Can you repeat the brand name of the sulfate/sulfite test strips you're using?

A: Quantofix

Q: Where do you get the sulfate test strips?

A: Amazon

Q: What would be considered "high" for a child when using the sulfate strips?

A: 10

Q: Can you expand on the use of sulfate test strips if/when oxalate markers aren't elevated on an Organic Acids Test? Would we expect to see low to no reported sulfate on the strip because of wasting?

A: Typically, in this scenario you will see high sulfate as the oxalate is being retained and the sulfate is being excreted.

Q: If oxalate crystals are insoluble in tissue, how can they dissolve to show up in the urine?

A: They are present in urine, not dissolved in it.

Q: Can urine be a false low?

A: Absolutely! Therefore we need to look for other clinical indications such as sulfate wasting.

Q: Can you repeat the gene that you mentioned that helps with sulfation?

A: SUOX

Q: And you suggested giving molybdenum?

A: Yes, it is the cofactor and can help when there are polymorphisms or when the transulfuration pathway is upregulated and sulfites are high.

Q: If you have high oxalates and positive for mycotoxins (i.e ochratoxin and gliotoxin) - which anti-fungal medication would you recommend starting + dosage and duration?

A: I would use an antifungal if there was evidence of colonization but am not a doctor and cannot prescribe. This also needs to be personalized for the individual. I do like Biocidin for these cases.

Q: How much baking soda are you recommending in water in between meals as prevention for oxalate dumping?

A: Very little; typically, ⅛ tsp

Q: How much Epsom salt do you typically recommend adding to a bath to help mobilize oxalates?

A: ¼c in a foot basin or 2 cups in a bath. There are sensitive individuals who do need to start more slowly.

Q: What is your favorite recommendation for dealing with fat malabsorption/digestion?

A: TUDCA and/or the combination of Quicksilver BittersX and Pure PC. Adding castor oil packs over the liver and gallbladder and using coffee enemas can be helpful if there is “sludgy” bile.

Q: Can oxalates pull calcium from bone and cause osteoporosis?

A: There are several studies exploring the associations between kidney stones and osteoporosis, but a causal link, to my knowledge, has not been clearly established. Please refer to Kidney Stones and Risk of Osteoporotic Fracture in Chronic Kidney Disease as well as Unravelling the links between calcium excretion, salt intake, hypertension, kidney stones and bone metabolism.

Organic Acids, Invasive Candida, Clostridia & More With Kurt Woeller, DO

The Great Plains Laboratory has been educating practitioners for over 15 years on how to help patients heal through cutting-edge testing, research and protocols. In our recent 2-Day OAT+TOX Workshop, speakers focused on the epidemic of environmental toxin exposure, from the many chemicals we encounter every day to mycotoxins released from mold. Attendees learned about many common environmental pollutants from the 173 chemicals tested by the GPL-TOX Profile.

The following Q+A is a grouping of responses from Kurt Woeller, DO, who participated in the OAT+TOX Workshop with his own unique topics and lectures as labeled.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


Kurt Woeller, DO

Kurt N. Woeller, D.O. has been an integrative and functional medicine physician and a biomedical autism specialist for over two decades. He is an author, lecturer and clinical practitioner offering specialized diagnostic testing and health interventions for individuals with complex medical conditions such as autism, autoimmune conditions, gastrointestinal and neurological disorders.

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Q: Can you see parasite infection on here and can that impact dopamine? Dopamine markers are elevated / too low but no clostridia in ASD child.

A: There is no specific marker absolutely diagnostic for parasites on the OAT. You would need to do stool testing.

Q: Hippuric acid - is this indicative of bacterial infection i.e. parasites?

A: It is indicative of increased normal digestive bacterial activity in the presence of chlorogenic acid found in many foods, e.g. fruits, potatoes, and other vegetables. There is a full list of foods in the interpretation section of the OAT.

Q: If 61 is high but no sweeteners in diet what could be the cause?

A: Often seen with bacterial markers found on page 1 of the OAT. Could also be phenols found naturally in foods.

Q: Is there an issue if ALL amino acid metabolites are low?

A: No. This section of the test is only significant when the values are elevated. This section of the OAT is to evaluate for certain metabolic diseases. Therefore, when the values are low it indicates that there is no evidence of a genetic disease linked to the specific marker.

Q: Ascorbic acid is extremely low in a child on a very high veg whole food diet - what would be the reason?

A: Ascorbic acid is commonly low on the OAT because it is an unstable acid in urine. The main reason the marker is on the OAT is to pick up on high values that might be associated with high oxalic acid.

Q: Do you recommend treating candida, when values are high, even if patient is asymptomatic?

A: Yes. I feel it is still worthwhile to treat.

Q: Does the high vitamin C ascorbic increase oxalate?

A: In some circumstances it might.

Q: Will uracil be elevated in those recently vaccinated?

A: I do not know. This would be a good thing for you to watch for in your practice.

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Q: If a person had pseudomonas aeriginosa and never took antibiotics for it, curing it naturally is there still the possibility of having a biofilm present?

A: Yes. It appears many of these bacteria produce biofilm as a natural part of their existence.

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Q: What is your opinion on the effectiveness of Botanical treatment versus Abx/Antifungal prescription medication?

A: It depends on what you are treating and how severe the condition is. I mostly try and use botanicals and reserve antibiotics for more severe conditions.

Q: I have a patient with 3 oxoglutaric acid which is listed in the intestinal overgrowth panel. He has elevated HPHPA and arabinose also. Is the 3 oxoglutaric different?

A: It gets produced from different types of intestinal yeast. Remember, candida is a type of yeast too, but there are different yeast species.

Q: What is the significance of 3-Oxoglutaric acid?

A: It gets produced from different types of intestinal yeast. Remember, candida is a type of yeast too, but there are different yeast species.

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Q: For fungal markers, do you do a course of binders and if no response prescribe?  What would make you add itraconazole/other antifungal?

A: I will typically add binders for any infections, e.g., candida, mold, bacteria. The use of Itraconazole would be based on the severity of the condition and known exposure to environmental mold. It is not a medication I will typically start with. I have seen good success with digestive mold, e.g., aspergillus, with oral Amphotericin B (from a compounding pharmacy).

Q: Has Dr. Woeller ever worked with people (children especially) with Bardot Biedl Syndrome (BBD)?  Parts of the Schizophrenia case seem similar to traits of this especially with inability to absorb or break down fats and low cholesterol.

A: I have not. In fact, I have never heard of this syndrome before. I will look into it.

Q: The question is about what trips the trigger to make him add the antifungals.

A: I am always going to treat yeast regardless of how high the OAT markers are. As a basic level this would be a botanical like Biocidin and probiotic. However, if I feel the severity of the condition warrants medications, I will use these too such as Nystatin. If I have a autistic child that is extremely yeast reactive such as inappropriate laughter, high self-stimulatory behavior, bloating, excessive flatulence than Nystatin may be needed. However, I have seen botanicals work too. As a general rule, I attempt botanicals first, then go with meds if these do not work.

Q: How do you treat a 2.5 year old with high arabinose, oxalic acid and quinolinic acid, mold exposure (+ penicillium)?

A: First, you need to find out if the mold exposure is causing high mycotoxins. The high oxalic should be addressed with a low oxalate diet and calcium/magnesium with meals, minimally. But, oxalic can often occur from mold exposure, so this needs to be addressed too. High arabinose is linked to invasive candida. Both the mold and candida might be able to be addressed with botanicals and probiotics. Medications are not my first option in most cases. The quinolinic acid can often be helped with niacinamide. This type of scenario is really based on the severity of the condition and what type of child we are supporting. Are they autistic? Do they have self-injurious behavior? How well do they take supplements? All of these questions and more need to be asked and determined before proceeding with any type of treatment program.

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Mycotoxins, Glyphosate, IgG Food Allergy Testing & More With William Shaw, PhD

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The Great Plains Laboratory has been educating practitioners for over 15 years on how to help patients heal through cutting-edge testing, research and protocols. In our recent 2-Day OAT+TOX Workshop, speakers focused on the epidemic of environmental toxin exposure, from the many chemicals we encounter every day to mycotoxins released from mold. Attendees learned about many common environmental pollutants from the 173 chemicals tested by the GPL-TOX Profile.

The following Q+A is a grouping of responses from William Shaw, PhD, who participated in the OAT+TOX Workshop with his own unique topics and lectures as labeled.

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


William Shaw, PhD

William Shaw, PhD, is board certified in the fields of clinical chemistry and toxicology by the American Board of Clinical Chemistry. Before he founded The Great Plains Laboratory, Inc., Dr. Shaw worked for the Centers for Disease Control and Prevention (CDC), Children's Mercy Hospital, University of Missouri at Kansas City School of Medicine, and Smith Kline Laboratories.

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Q: How long should someone be on a binder?

A: Binders should be utilized for the duration of the mold exposure and treatment.

Q: Only antifungal treatments for removing mold from lungs and nasal passages?  I have heard/seen that nebulized GSH and nasal irrigation with specific sprays gets rid of it. Evan Brand discusses alternatives to antifungals as he got rid of his severe mold infection without using them.

A: These can be utilized. It is not guaranteed that these therapies alone will be enough in each case. Antifungals should be considered in each case where needed.

Q: Can you speak to products like XClear vs nasal Glutathione for sinus colonization? Also, oral Amphotericin, …is it more/less/equal in efficacy to oral nystatin for GI mold/yeast? (I know IV it can be really harsh).

A: Both Xlear and nasal Glutathione can work to clear nasal colonization. They also can work well together. Amphotericin can work well for GI mold. It is more beneficial than Nystatin when nasal/respiratory colonization is involved as Nystatin doesn’t get absorbed by the GI tract.

Q: Why would a patient have a Mycophenolic Acid in the high abnormal range (302.17) if he is not taking an immunosuppressant drug and does not have an autoimmune disease? He does think he has a penicillin allergy and hasn’t had penicillin since childhood. How is the high Mycophenolic Acid treated in such a case?

A: Mycophenolic acid will be in the high range if there is a current exposure to penicillium mold in foods and/or a water damage building. Also if there is a high colonization and that mold is producing large amounts of the toxin you can see elevated levels. Typically, if someone is on the immunosuppressant prescription you would see this value closer to the >10,000 range.

Q: What has been used in place of Cholestyramine if the patients are unable to tolerate it?

A: You can try Welchol or charcoal. These have similar binding affinities.

Q: What is the dosage of Cholestyramine for children?

A: The research dose is 240mg/kg/day in 2-3 divided doses. It usually evens out to 8g total per day. LINK

In most cases this is a lot for a child to handle. You can always divide this dose in half to 2g one to two time a day.

Q: Can you discuss how you dose binders like charcoal & clay?

A: These binders should be dosed according to the client’s bowel movements. Most products recommend 2 caps for about 500mg give or take. If someone has normal bowel movements this should be a suitable dose for them. If constipation is an issue, then only use 1 capsule a day and be sure that they are having a regular movement every day they take the binder. If diarrhea is an issue, consider using 2 capsules 2 times a day to slow gastric movement and allow for nutrients to have increased time in the GI tract for enhanced absorption. Be sure they are giving away meals/meds/supplementation. 2 hours on each end is usually suitable. 4-6 hours is ideal to ensure no interaction. Some find it best to give before bed 2 hours after dinner or first thing in the morning and waiting a couple hours to eat breakfast.

Q: So to clarify, you don't recommend any type of provocation before a urine mycotoxin test?  I understood that a completely negative test just meant that there was no provocation.

A: Correct there is no need to provoke our MycoTOX profile. A completely negative test usually means the mycotoxins the person was exposed to were not tested by our assay.

Q: Would a person who has a penicillin allergy by infected be penicillium?

A: A penicillin allergy differs from an overgrowth of Penicillium mold. There is a specific protein from the mold organism that penicillin is made from. This is specific to a penicillin allergy. This differs from a mold exposure. An exposure won’t necessarily make you allergic to penicillin.

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Q: Do you know if general anesthetic gases show up in any of the compounds measured on the GPL-TOX?  Wondering if anesthesia providers measure higher in any of these?

A: If it is administered intravenously, phthalates may be present (Marker number 3.). This chemical is also present in some pharmaceuticals, depending on the compound used.

Q: At what temperature should the sauna be for best treatment? What if patient is unable to tolerate high temps but can tolerate 130 degrees?

A: The main function of utilizing sauna in detoxification is to increase internal body temperature to help liberate toxins from adipose tissue and increase perspiration for a route of elimination. Whatever temperature that happens for the patient should be utilized. It may need to be started slow and progress as tolerated.

Q: Do you include in the testing kits urine bags for infants? Can infants be tested with the EnviroTOX Complete Panel with one sample too?

A: Infants can be tested, and to ensure you receive the urine bags, request them at the time you order the test kit.

Q: Do you recommend traditional or infrared sauna?

A: When the original research was being conducted on this method as a part of detoxification, the original saunas were utilized. Infrared is now the preferred, but traditional will still work.

Q: Sauna at what temp for one hour?

A: What ever the patient can handle that will induce perspiration.

Q: Is an infrared suana effective in detoxing bromopropane?

A: Yes, along with Glutathione or NAC. 

Q: How long should a patient stay in sauna a day?

A: That is dependent on the patient, and what they can tolerate.

Q: Can you repeat the recommendation for IR sauna?  How many times per week?  For how long?

A: 1 hour, daily, for 6 weeks

Q: Where do you find glyphosate on the GPL-TOX report?

A: It is not on the GPL-TOX, it is a separate test

Q: The 40 Year old male with high glyphosate and HVA/VMA ratio was also on a dopamine/norepinephrine reuptake inhibitor. How do you interpret the OAT given this circumstance?

A: Pharmaceuticals acting in the synaptic cleft are not likely to influence urinary metabolites more than daily variability.

Q: Are there significant amount of glyphosate in marijuana? I have several patients using cannabis who presented with dysbiosis.

A: Depending on the source there could be trace levels of it, but not likely sprayed on the plant or flower itself, as it would kill the plant (or a weed in some agricultural communities).

Q: what do you think of Ion Cleanse foot bath detox?

A: Clinicians and patients have reported some benefits from it, but beyond anecdotal evidence, the very limited research does not favor it.

LINK

Q: I have an infrared sauna in my home office and have my cancer patients use it. What is the fear of cross contamination from chemo drugs being excreted in sweat passing to others? We use towels and burn off with 10 minutes of 150degree heat  in between people. hoping that is

A: That will vary greatly depending on the chemo agent used. In general, chemotherapy drugs take 48-72 hours to leave the system, and some can be excreted through sweat. Caution is advised for using sauna treatments with patients actively on chemo agents.

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Q: I've tested a patient wth know history of food allergies. Nothing showed so we did IgE since she has high eosinophil/histamine response. Again, nothing showed. All patients -4 -people I’ve tested showed zero allergens. This has not given me confidence in the testing. Thoughts?

A: There are a multitude of variables that could explain this, so I would recommend taking one or two of these tests, and discussing it with one of our consultants.

Q: How long do should gluten be reintroduced prior to doing the Food IgG test?

A: This depends on the individual’s response, but generally around a week prior to testing should suffice. 

A: Do you have a recommendation to detox from gluten after exposure?

Q: You can add enzymes to help break it down quicker, or a binder to help adsorb it in the gut if an accidental exposure occurred.

Q: IgG4 is used to detect autoimmune pancreatitis. Why do you say it’s not involved in inflammation?

A: IgG1-3 do not exchange heavy and light chains with other antibodies to form specific antibodies, allowing them to create inflammation. Once these immunoglobin antibodies bind to food antigens, they form larger immune complexes, and increase the inflammation. IgG4 antibodies to food antigens show  the presence of antibodies to food, and therefore an immune response, but they will not usually cause inflammation.

Q: Is there a difference between testing dried blood vs whole blood?

A: Mainly in the ease of obtainment of sample. Comparisons of both have been found to be equally valid. LINK

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Mycotoxin Properties and Metabolism: Part 1


By LINDSAY GODDARD, MS, RDN, LD

It appears mycotoxins are gaining a significant amount of interest as the literature increases on their toxic effects on humans and other animals. Just with any topic, as more data surfaces, more questions arise. Mycotoxin sources, testing, impacts, and treatments have been discussed in other blogs that you can review.

What has received less attention is how these compounds behave, particularly within our bodies, and what levels are commonly observed. The latter being particularly ambiguous.  In this article, properties and the metabolism of the top four most common mycotoxins will be explained to help further understand their behaviors, along with common ranges that are typically observed in Great Plains Laboratory. It is important to keep in mind that most of this research is done within the agriculture communities and laboratories, since human evaluations can be difficult to assess, for obvious reasons. It is the intent to use as much data from human studies as possible, but it may not always be feasible. It is also important to understand that although the typical ranges are provided, this does not assess the severity of those mycotoxins to an individual. Humans and other animals deal with these mycotoxins very differently, and it appears to be highly individualized within the species and current state of health of the individual.

Ochratoxin A (OTA) is the most common mycotoxin to show up on the test. Average positive ranges are generally from 15-30 nanograms/g of creatinine for people who are suspicious of mycotoxins. Results have been shown to be much higher in more extreme cases, with levels reaching up into the hundreds and even thousands range.

Toxicology

OTA is most notably a nephrotoxin, especially as it relates to the proximal tubule, which has been observed in several phylums. It also can impact the immune system; however, the exact mechanism is variable among different species. Studies have been observed the presence of OTA and the depletion of lymphoid cells, and stimulation of cytokine production especially with IL-2 and IL-5. Other influences are linked to inhibition of various enzymes such as phenylalanine hydroxylase, phenylalanine-tRNA synthetase, renal phosphoenolpyruvate carboxykinase, and carboxypeptidase A. OTA also can enhance lipid peroxidation, which is another aspect of the cellular damage caused by this mycotoxin. It also has the potential to cause proliferation of the cell via the interference with hormonal Ca2+ signaling, and therefore impairing Ca2+ cAMP homeostasis. 

Properties

Structurally, OTA consists of a para-chlorophenolic group, which contains a dihydroisocoumarin moiety, which is linked to L-phenylalanine via an amide link. At a neutral pH, OTA is slightly soluble in water, and soluble in polar organic solvents. Once alkaline conditions occur, it becomes soluble in all the aqueous solutions. Its melting point is between 90 °C (194 °F) to 169 °C (336.2 °F) depending on the solvent, proving it’s high stability especially in food processing.

Metabolism

It is absorbed into the system, via oral, skin or inhalation routes. From the ingestion standpoint, OTA is absorbed in the GI tract through various points. Taking note that the hydroxyl group of OTA is more in the nonionized form at low pH, which improves its absorption, therefore a significant amount of OTA is absorbed in the stomach. It is also readily absorbed in the intestines via passive diffusion, which is aided by the OTA binding to serum albumin. This complex also increases the half-life with a single dose of OTA lasting about 35 days. It is thought that this binding capacity is what allows OTA to transfer from blood to milk.

The human body attempts to eliminate some OTA via the bile, however enterohepatic recycling makes that less efficient. Once in the liver, the cytochrome P-450 microsomes along with NADPH, metabolize OTA further into hydroxyochratoxin A for elimination.  OTA itself is mainly excreted through the urine, yet the organic anion transport system in the proximal and distal tubules of the kidney actively reabsorb OTA. At this point, OTA is being transported with smaller carrier proteins, which allow the compound to pass through the glomerular membrane at an increased rate. This further increases the bioaccumulation and contributes to the extended half-life, leading to the cause of the nephrotoxicity that ensues with consistent, larger exposures.

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Mycophenolic Acid (MPA) is one of the better understood mycotoxins within the medical community since it is used by the pharmaceutical industry. The average positive range tends to be between fifty and the mid hundreds. In more extreme cases, it can be in the thousands. If someone is taking the drug that contains MPA, the amount excreted tends to be between 40,000-100,000 nanograms/g of creatinine.  

Toxicology

The main mechanism of action for MPA is as an inhibitor of inosine monophosphate dehydrogenase, leading to an inhibition of the de novo pathway of guanosine nucleotide synthesis. This significantly reduces T- and B- lymphocytes since they are dependent on de novo synthesis of purines for their proliferation.

Properties

MPA is a polyketide compound, which is not soluble in water, and has a melting point around 141 °C (285 °F). Similar to OTA, it has a high affinity for albumin. When albumin is in lower amounts because of a disease or inflammatory state, the free MPA concentration may increase.  MPA is metabolized by glucuronidation via glucuronyl transferase, primarily in the liver, but also in the intestines and kidney. This ultimately forms MPA glucuronide (MPAG). This metabolite has little activity on the immune system, however the other metabolite that is formed, acyl glucuronide, will also impact the immune system, similarly to MPA. When analyzing the metabolism of MPA in stable transplant patients, 28% of the MPA taken orally was converted to MPAG, and the ratio of MPA:MPAG:acyl glucuronide was about 1:24:0.28.  

Metabolism

MPA, as observed through oral administration, is absorbed in the small intestines, and primarily eliminated in the urine by active tubular secretion and glomerular filtration, with approximately 60% or more as MPAG, and about 3% as MPA. Keep in mind here that the MPAG has less impact on the immune system versus the MPA, so measuring that would have less clinical significance as it relates to assessing toxicity. MPAG also utilizes bile in its elimination, however it can be deconjugated by certain flora in the gut back to MPA, leading it to be reabsorbed. Some of the enzymes involved in MPA glucoronidation (particularly UGT1A8 and UGT1A9), are expressed outside of the liver, thus contributing to the metabolism within the GI tract. The half-life of MPA is between 8-16 hours, therefore when extreme elevations are occurring, it is likely from a very recent exposure.

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Previously known as F-2, Zearalenone (ZEA) is another mycotoxin that has a large amount of recognition. It is a very common contaminate of grains to the point it is regulated closely by numerous countries. What sets it apart from other mycotoxins is that it has a unique application in regulating hormones in livestock due to its estrogenic effects. This pharmaceutical drug is called zeranol and is approved to be used in livestock within the US, though the FDA has banned it for human use. It should be noted here that the World Anti-Doping Agency has been tracking zeranol since 2003 in athletes (who typically consume a significant number of livestock products) and has only found 6 positive tests globally. Typical ranges found on the GPL MyCoTOX Panel tend to be below 20, and in more extreme cases, can get up in the hundreds or above.

Toxicology

ZEA’s main mechanism of action is activating estrogenic receptors, creating estrogenic responses. It is therefore classified as an endocrine disrupter. The impact of ZEA on estrogenic effects varies significantly throughout animal species. Swine tend to be the most sensitive to it, while humans require a more chronic exposure to be significantly harmful. Cascading effects have been identified in the uterine organ and mammary tissue, like estradiol elevations.  ZEA also has the capacity to act on the hypothalamus and pituitary, mimicking estrogenic effects. There is some discussion of its association with hepatotoxicity and immunotoxicity, but these are not as well understood.

Properties

The structure of ZEA is a phenolic resorcylic acid lactone and is extremely similar to the estradiol structure. There are various forms, with at least seven derivatives identified just with corn, alone. They have all been shown to impact estrogen receptors. It has a melting point of 164 °C (328 °F), and solubility in water is very limited (0.002g/100mL). However, it is soluble in various solutions, particularly in aqueous alkali. ZEA is fairly heat stable but can be partially destroyed with extrusion cooking. The heat degradation is dependent on the solution it is in, but overall, it is completely degraded at 225 °C (437 °F). It is half-life from oral dosage is approximately 86 hours in swine, and 72 hours in hens. Not much information exists on humans except for one study by Mukherjee et al. where it was estimated to be around 11.98 hours in young girls. It has been shown to bioaccumulate within adipose tissue and reproductive tissue of females, and interstitial cells within the testes. 

Metabolism

Ingestion or inhalation seems to be the most common routes of exposure, though ZEA does have the ability to permeate through human skin. Absorption of ZEA occurs within the intestinal lumen for most animals. In swine observations, somewhere between 80-85% was absorbed through a single dose. ZEA is mainly conjugated through glucaronidation in the liver and the intestinal mucosa. It then goes through enterohepatic circulation and biliary excretion, with stool being the major route of elimination. Rumen and microbiota metabolism is also a potential; however, this is dependent on absorption, enzymes, and receptor availability and/or presence in particular species.

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Citrinin (CTN) is likely the second most common mycotoxin to be reported, but unfortunately it has the least amount of recognition in the literature. It is very common to find alongside OTA, especially since they typically come from the same species (Aspergillus niger). General ranges found for positive results are below a hundred. 

Toxicology

The mechanism of action for CTN toxicity is not as well understood as the other mycotoxins. It has been found to cause oxidative stress and increased permeability of mitochondrial membranes, however, not cellular membranes themselves. In these mitochondrial preparations, CTN inhibited succinate oxidase and NADH oxidase, while also completely inhibiting cellular respiration.  The target organ appears to be the kidney in a variety of phylums. Embryocidal, fetotoxic, and genotoxic have been suspected, and proven in some organisms. Immunotoxicity and hepatotoxicity is also a potential, but data is lacking. When CTN and OTA are together within the system, they work cooperatively in reducing the activity of RNA synthesis in the renal tissue.

Properties

CTN is a polyketide mycotoxin that is insoluble in cold water, barely soluble in hot water, and soluble in polar organic solvents. It can breakdown in acidic and alkaline solutions. CIT’s melting point is around 100 °C (212 °F).  Relative to other mycotoxins, CTN is fairly heat sensitive, and unstable in temperature elevations. When heated (>175 °C, in dry conditions, >100 °C in water), it has the potential to degrade to CIT H1, which is more toxic, and CIT H2, which is less toxic, than CTN. It also has a short half-life in the human blood (~9 hours), and in urine (6-8 hours), and for this reason, it is thought it does not bioaccumulate in organisms unless there is repeated, large exposures.

Metabolism

Oral, inhalation, and skin tend to be the major routes of exposure. Unfortunately, there is very limited data as to the exact route and elimination of CIT in humans, however excretion moves through the kidney’s, which is where it has the potential to bioaccumulate.


Stay tuned for part II, where the next review will be of the less common, but potentially more toxic, group of mycotoxins measured on the MycoTox. 


References

1. Gupta, Ramesh C. Veterinary Toxicology. Basic and Clinical Principles 3rd edition. 2018. 
2. Khoury A and Atoui A. Ochratoxin A: General Overview and Actual Molecular Status. Toxins. 2010. 2(4): 461-493. PMID: 22069596
3. Plumlee KH. Mycotocins Toxicokinetics. Clinical Veterinary Toxicology. 1st Edition. 2004
4. Gruber-Dorninger C., Novak B, Nagl V, and Berthiller F. Emerging Mycotoxins: Beyond Traditionally Determined Food Contaminants. Journal of Agricultural and Food Chemistry2017 65 (33), 7052-7070. SOURCE
5. Food and Drug Association. Mycophenolic acid (Myfortic). SOURCE
6. Lamba V, Sangkuhl K, Sanghavi K, Fish A, Altman RB, and KE.PharmGKB. Mycophenolic Acid Pathway. Pharmacogenetics and genomics.2014. PMID:24220207. SOURCE
7. Hooijmaaijer E, Brandl M, Nelson J, Lustig D. Degradation products of mycophenolate mofetil in aqueous solution. Drug Dev Ind Pharm. 1999 Mar;25(3):361-5. doi: 10.1081/ddc-100102183. PMID: 10071831.
8. Haschek WM, Voss KA,  Beasley VR.  Selected Mycotoxins Affecting Animal and Human Health. Handbook of Toxicologic Pathology (Second Edition).2002. Pages 645-699. SOURCE
9. United States Anti-Doping Agency. Zeranol FAQ. 2021. SOURCE
10. National Center for Biotechnology Information (2021). PubChem Compound Summary for CID 5281576, Zearalenone. SOURCE
11. Ryu D, Hanna MA, Eskridge KM, and Bullerman LB. Heat Stability of Zearalenone in an Aqueous Buffered Model System. Journal of Agricultural and Food Chemistry 2003 51 (6), 1746-1748. DOI: 10.1021/jf0210021. 
12. Gil-Serna J, Vázquez C, Patiño B. Mycotoxins | Toxicology. Reference Module in Food Science. Elsevier. 2019. ISBN 9780081005965. SOURCE
13. Doughari, J. The Occurrence, Properties, and Significance of Citrinin Myctoxin.  Plant Pathol Microbiol 2015, 6:11 DOI: 10.4172/2157-7471.1000321
14. Arce-López B, Lizarraga E, Vettorazzi A, González-Peñas E. Human Biomonitoring of Mycotoxins in Blood, Plasma and Serum in Recent Years: A Review. Toxins (Basel). 2020;12(3):147. Published 2020 Feb 27. doi:10.3390/toxins12030147

8 Binders for Mycotoxins

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BY JASMYNE BROWN, ND, MS

After a positive Organic Acids Test and MycoTOX Profile, the presence of mold and mycotoxins are usually significant answers for many symptomatic clients. When working with mycotoxicosis, choosing the correct binder can present a challenge.  Oftentimes I get the question: which binder is correct for which toxin? Since the research for the binding capacity of each binder isn't as heavily researched as other agents, it can be daunting to sift through the information. Below is a collection of research connecting mycotoxins to a good binder choice.

In our bodies, toxins are detoxed and excreted through a few pathways. Routes of elimination include urine, stool, bile and through our skin. Other routes include tears and saliva but are negligible in the realm of detoxification. Another route is breast milk. Since breast milk is a route of excretion this means toxins can be transferred to another life this way. This fact makes binders even that much more crucial in childbearing age women.

When it comes to binders, bile and stool are the target routes of elimination. Fat soluble substances such as dietary lipids, certain vitamins and fat-soluble toxins like mycotoxins get packaged into bile for absorption and detoxification. During bile’s life cycle it gets excreted into the GI tract and is what gives stool its brown color. In the colon most of the bile is reabsorbed so the liver and gallbladder do not have to work as hard to make more bile. It is recycled and reused. Dysfunction of this phenomenon, bile acid malabsorption, chronic diarrhea is the main symptom.  Since bile is reabsorbed, in the ileum and jejunum, if toxins are packaged in the bile then the toxins can be reabsorbed as well. They would then re-enter circulation via the hepatic portal system. This is where binders come in handy. Binders will adhere to the bile that packages the toxins and then it cannot be reabsorbed. Due to the nature of this adherence, it cannot be trusted that the bond is irreversible. This bond is more like static cling, as described by Dr. Neil Nathan. The lack of a tight bond allows for the bile to be released if not excreted regularly. Meaning, irregular bowel movements from constipation, lack of fiber, or motility issues could cause resorption of toxins even with binder usage. Binders by nature are constipating and this should be mitigated and assessed regularly during binder usage. Properly moving bowels through diet and supplements should be achieved prior to adding in any binding agent. View products for gut motility on the New Beginnings Nutritionals Website

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In the world of prescriptions, cholestyramine and colesevelam hydrochloride, more commonly known as Welchol, are often binders of choice. They are known for their intended use and design, which is their lipid lower activity and use in glycemic control in patients with type 2 diabetes mellitus. They work by directly binding bile in the GI tract. This causes a reduced bile resorption and an increased conversion of cholesterol to bile, via 7a-hydroxylation, thus lowering cholesterol levels. In this process toxin laden bile is bound and thus excreted via stool.

These two binders are often used in mycotoxin detoxification protocols. As seen above, this is for good reason. The mycotoxin that responds best to these prescriptions is ochratoxin a (OTA), according to the research. This is a notorious mycotoxin. OTA is produced by many species of Apergillus and Penicillium molds. These are two of the most ubiquitous molds in the environment. This fact makes OTA the most common mycotoxin. It is so common that even regular ingestion of commonly moldy foods will most likely expose you to small, negligible amounts of OTA - We outline this in our article: Mycotoxins in Food. In cases of water damage building exposure these drugs are valuable assets to binding this mycotoxin. 

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A few years ago, activated charcoal was the new buzz trend. It was popping up in drinks, snacks, even ice cream. Due to this most people are familiar with this binder. It is commonly used for firming loose stools, binding toxin from food poisoning, and now for mycotoxin binding. According to the research most binders will bind to just about anything, including nutrients necessary for life. They are non-discriminating. This fact made the charcoal trend rather troubling for those engaging in high intake of this substance with no regard to its potential danger if not taken responsibly. But, due to this, activated charcoal is an effective toxin binder to just about any toxin that is excreted in the gut. It works similarly to cholestyramine by adsorbing to toxins packaged in bile.

Research shows that in food stuff and in the body activated charcoal is beneficial in mycotoxin binding. OTA is bound effectively by charcoal products. This a good alternative for non-prescribing practitioners. Charcoal has also shown efficacy in adsorbing to macrocyclic trichothecenes. Two of the most common are verrucarin a and roridin e, and these are assessed on the MycoTOX Profile. Other subvarieties of verrucarin, including ‘J’ have shown binding efficacy with charcoal administration. Also T-2 toxins from fusarium are bound by charcoal.

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Another common binding agent is bentonite clay and zeolite clay. These two clays have been touted as working wonders in the cosmetic arena by pulling toxins from the skin. These clays have been shown to bind greatly to toxins in animal feed, reducing the toxic load before consumption. Another clay is montmorillonite clay, also known as Novasil. This clay has ample research as a mycotoxin adsorbent in animal feed, a highly mycotoxin contaminated source. Great news, these clays do the same adsorbing action in the GI tract. Both agents show great affinity for binding aflatoxins best. These clays do not have much other research connecting them as strong adsorbents to other toxins as they do with aflatoxins. Although they can be useful in clients with these toxins and zearalenone, OTA, and gliotoxin as there is some adsorbing activity with these toxins.

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This water-soluble polysaccharide is a well touted weight loss solution. It comes from the elephant yam, konjac. It is a hemicellulose fiber with beta-D-glucose and beta-D-mannose with acetyl groups with beta 1–4 linkages. Due to the lack of enzymes in human saliva to break these linkages, glucomannan goes through the GI tract unchanged. This allows for it to bind without absorption. Due to its content, this fiber can adsorb up to 50 times its weight. Glucomannan has shown efficacy in binding various mycotoxins.  Aflatoxin and OTA are major toxins affected by this binder. Others include zearalenone and Toxin T-2. not much efficacy was seen in binding DON-1 (Deoxynivalenol). Since glucomannan is a fiber this may be an option to consider in more constipated clients with ample water intake.

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Speaking of fiber, in general fibrous supplements and foods can act as simple overall binders. Fiber from oats, wheat bran, alfalfa, lignans in flax and chia, guar gum, etc have been used as early interventions in lowering cholesterol. It has the same effect that cholestyramine has on cholesterol. It is due to the bile sequestering activity of these fibers that work to lower cholesterol. In turn this will also lower toxic load. Even though fiber doesn't have much direct research in the binding of specific mycotoxins, it is always a good dietary change to implement. Barley and oats showed highest absorptive capacity amongst other fibers when tested. Another great fiber binder to consider is modified citrus pectin (MCP). This binder has shown great efficacy in binding heavy metals such as lead. Though this isn't a mycotoxin, this shows us that MCP has a great potential utility in any detox protocol.

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This next binding agent is a common plant-based agent. Chlorella is a type of freshwater algae that is packaged into a tablet, liquid extracts, and powders. It is often touted as a superfood due to its highly nutritious profile. It is high in protein, vitamins A, C, and E and is a great source of fiber. Because of its nutrition, chlorella is known for its wound healing, anti-cancer, anti-aging, and immune boosting potential. In breastfeeding mother’s chlorella intake increased circulating immunoglobulins in breast milk. This plant is great as a heavy metal binder and as a binder of aflatoxins. It has even been shown to inhibit aflatoxin B1 induced liver cancer.

Due to the safety profile of chlorella, it is a great binder for all populations. It is difficult to detox a constipated child or a woman expecting a child and is planning to breastfeed. Since so many other binders bind not only toxins, but also nutrients it can be difficult to support detox. Adding in small doses of chlorella is a safe and effective way to add in supportive detox without stimulating too much toxin release to the unborn fetus or breastfeeding child. 

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Humic acid and its related counterpart, fulvic acid, are the final products of decomposition of organic matter. They are formed through humification of plant and animal matter via biologic processes of microorganisms. This byproduct acts as an adsorbent in soil to bind to toxic substances. Agriculturalists use these substances as soil additives to boost the growth and health of their crop due to its concentrated amount of nutrients. Due to its rapid lifecycle humic acid doesn't compete for nutrients with the plant or any other organism that uses it. This makes this biotoxin binder simpler to utilize when taking a variety of nutritional supplements.

Not only is humic acid a great biotoxin binder, but it also has shown efficacy as an anti-inflammatory. It also has shown promise in stimulating apoptosis in promyelocytic leukemia cells. This substance, along with fulvic acid, is a wonderful well-rounded addition to any detoxification protocol. 

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This section of biotoxin binders may come as a surprise. Probiotics are best known for their activity in repopulating the GI microbiome after antibiotic use, killing of pathogenic organisms like C. difficile, and as a support in a whole host of chronic diseases. What many do not realize is that these organisms can also directly bind to mycotoxins. Strain of lactobacillus work to directly bind aflatoxins especially the B1 variety. The specific strains are L. pentosus and L. beveris. Another promising strain is L. plantarum C88. This strain works not only to bind to aflatoxins, but it also works by upregulating the antioxidant activity of glutathione s- transferase. It also shows great binding capacity to the common mycotoxin, sterigmatocystin.

Strains of saccharomyces also work well to bind mycotoxins. S. cerevisiae has been shown to bind tightly to aflatoxins. It has also shown great efficacy to bind to OTA and zearalenone. Saccharomyces boulardii, clinically, has shown great efficacy against gliotoxin. It has also shown efficacy in reducing Aspergillus and Fusarium molds in the GI tract. This will indirectly reduce mycotoxins, as it is reducing the producers of mycotoxins including zearalenone, enniatin b, OTA, gliotoxin, and aflatoxins. Mannan oligosaccharides (MOS) are prebiotics derived from the outer cell wall of S. cerevisiae. This prebiotic has been shown to bind to citrinin, which a wide variety of molds produce.  Using a variety of these strains will round out not only your gut treatment but also the detoxification process.


All in all, binding agents are an integral part of mycotoxin illness detoxification. Whether someone has 1 or 10 mycotoxins populate on the MycoTOX Profile, having the correct binders can be a challenge. Hopefully, this can be used as a resource to guide you in planning toxin binder regimens to best help your clients. Using a combination of binding agents will allow for well-rounded binding capacity in any mycotoxin toxicity case. View a wide variety of binding agents at New Beginnings Nutritionals to support you in choosing the best biotoxin binders.

This is a table matching mycotoxin with binders that have research to their binding affinity

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References

1. Agawane, S. B., and P. Lonkar. “Effect of Probiotic Containing Saccharomyces Boulardii on Agawane, S. B., and P. Lonkar. “Effect of Probiotic Containing Saccharomyces Boulardii on Experimental Ochratoxicosis in Broilers: Hematobiochemical Studies.: Semantic Scholar.” Undefined, 1 Jan. 1970, SOURCE. 
2. Ardeshir Mohaghegh,Mohammad Chamani,Mahmoud Shivazad,Ali Asghar Sadeghi &Nazar Afzali. “Effect of Esterified Glucomannan on Broilers Exposed to Natural Mycotoxin-Contaminated Diets.” Taylor & Francis, SOURCE. 
3. Armando, M.R., et al. “Adsorption of Ochratoxin A and Zearalenone by Potential Probiotic Saccharomyces Cerevisiae Strains and Its Relation with Cell Wall Thickness.” Journal of Applied Microbiology, vol. 113, no. 2, 2012, pp. 256–264., doi:10.1111/j.1365-2672.2012.05331.x. 
4. “Chlorophyll and Chlorophyllin.” Linus Pauling Institute, 1 Jan. 2021, SOURCE. 
5. D. Lloyd-Jones, R. Adams, et al. “Impact of Daily Chlorella Consumption on Serum Lipid and Carotenoid Profiles in Mildly Hypercholesterolemic Adults: a Double-Blinded, Randomized, Placebo-Controlled Study.” Nutrition Journal, BioMed Central, 1 Jan. 1970, SOURCE. 
6. De Mil, Thomas, et al. “Characterization of 27 Mycotoxin Binders and the Relation with in Vitro Zearalenone Adsorption at a Single Concentration.” Toxins, MDPI, 5 Jan. 2015, SOURCE. 
7. Devreese M;Girgis GN;Tran ST;De Baere S;De Backer P;Croubels S;Smith TK; “The Effects of Feed-Borne Fusarium Mycotoxins and Glucomannan in Turkey Poults Based on Specific and Non-Specific Parameters.” Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association, U.S. National Library of Medicine, SOURCE. 
8. El Khoury, Rhoda, et al. “OTA Prevention and Detoxification by Actinobacterial Strains and Activated Carbon Fibers: Preliminary Results.” MDPI, Multidisciplinary Digital Publishing Institute, 24 Mar. 2018, SOURCE. 
9. Garcia Diaz, Tatiana, et al. “Use of Live Yeast and Mannan-Oligosaccharides in Grain-Based Diets for Cattle: Ruminal Parameters, Nutrient Digestibility, and Inflammatory Response.” PloS One, Public Library of Science, 14 Nov. 2018, SOURCE. 
10. Guo M;Hou Q;Waterhouse GIN;Hou J;Ai S;Li X; “A Simple Aptamer-Based Fluorescent Aflatoxin B1 Sensor Using Humic Acid as Quencher.” Talanta, U.S. National Library of Medicine, SOURCE. 
11. Hamidi, Adel, et al. “The Aflatoxin B1 Isolating Potential of Two Lactic Acid Bacteria.” Asian Pacific Journal of Tropical Biomedicine, vol. 3, no. 9, 2013, pp. 732–736., doi:10.1016/s2221-1691(13)60147-1. 
12. Hope, Janette. “A Review of the Mechanism of Injury and Treatment Approaches for Illness Resulting from Exposure to Water-Damaged Buildings, Mold, and Mycotoxins.” The Scientific World Journal, Hindawi, 18 Apr. 2013, SOURCE. 
13. J;, Santos RR;Vermeulen S;Haritova A;Fink-Gremmels. “Isotherm Modeling of Organic Activated Bentonite and Humic Acid Polymer Used as Mycotoxin Adsorbents.” Food Additives & Contaminants. Part A, Chemistry, Analysis, Control, Exposure & Risk Assessment, U.S. National Library of Medicine, SOURCE. 
14. Jay Y. Jacela, DVM; Joel M. DeRouchey, PhD; Mike D. Tokach, PhD; Robert D. Goodband, PhD; Jim L. Nelssen, PhD; David G. Renter, DVM, PhD; Steve S. Dritz, DVM, PhD. Fact Sheet: Mold Inhibitors, Mycotoxin Binders, and Antioxidants, SOURCE. 
15. Jubert, Carole, et al. “Effects of Chlorophyll and Chlorophyllin on Low-Dose Aflatoxin B(1) Pharmacokinetics in Human Volunteers.” Cancer Prevention Research (Philadelphia, Pa.), U.S. National Library of Medicine, Dec. 2009, SOURCE. 
16. Kerkadi A;Barriault C;Tuchweber B;Frohlich AA;Marquardt RR;Bouchard G;Yousef IM; “Dietary Cholestyramine Reduces Ochratoxin A-Induced Nephrotoxicity in the Rat by Decreasing Plasma Levels and Enhancing Fecal Excretion of the Toxin.” Journal of Toxicology and Environmental Health. Part A, U.S. National Library of Medicine, SOURCE. 
17. Kraljević Pavelić, Sandra, et al. “Critical Review on Zeolite Clinoptilolite Safety and Medical Applications in Vivo.” Frontiers in Pharmacology, Frontiers Media S.A., 27 Nov. 2018, SOURCE. 
18. Kumar, C. B. ; Reddy, B. S. V. ; Gloridoss, R. G. ; Prabhu, T. M. ; Suresh, B. N. “ Effect of MOS Based Toxin Binder on Low Level Citrinin Toxicity in Commercial Broilers.” Mysore Journal of Agricultural Sciences, vol. 48, no. 1, 2014, pp. 75–82. 
19. L,Haus M;Žatko D;Vašková J;Vaško. “The Effect of Humic Acid in Chronic Deoxynivalenol Intoxication.” Environmental Science and Pollution Research International, U.S. National Library of Medicine, SOURCE. 
20. Lauterburg BH, Dickson ER, Pineda AA, Carlson GL, Taswell HF. “Removal of Bile Acids and Bilirubin by Plasmaperfusion of U.S.P. Charcoal-Coated Glass Beads.” Europe PMC, 30 Sept. 1979, SOURCE. 
21. Li, Yan, et al. “Research Progress on the Raw and Modified Montmorillonites as Adsorbents for Mycotoxins: A Review.” Applied Clay Science, Elsevier, 30 July 2018, SOURCE. 
22. Naumann, Susanne, et al. “In Vitro Interactions of Dietary Fibre Enriched Food Ingredients with Primary and Secondary Bile Acids.” Nutrients, vol. 11, no. 6, 2019, p. 1424., doi:10.3390/nu11061424. 
23. Riaz, Sana. “Cholestyramine Resin.” StatPearls [Internet]., U.S. National Library of Medicine, 25 May 2020, SOURCE. 
24. Rotter, R G, et al. “Influence of Dietary Charcoal on Ochratoxin A Toxicity in Leghorn Chicks.” Canadian Journal of Veterinary Research = Revue Canadienne De Recherche Veterinaire, U.S. National Library of Medicine, Oct. 1989, SOURCE. 
25. Vahouny, George V., et al. “Dietary Fibers: V. Binding of Bile Salts, Phospholipids and Cholesterol from Mixed Micelles by Bile Acid Sequestrants and Dietary Fibers.” Lipids, vol. 15, no. 12, 1980, pp. 1012–1018., doi:10.1007/bf02534316. 
26. “Verrucarin A (T3D3720).” T3DB, SOURCE. 
27. S,Baker; W,Shaw. “Case Study: Rapid Complete Recovery From An Autism Spectrum Disorder After Treatment of Aspergillus With The Antifungal Drugs Itraconazole And Sporanox.” Integrative Medicine (Encinitas, Calif.), U.S. National Library of Medicine, SOURCE. 
28. Wang JS;Luo H;Billam M;Wang Z;Guan H;Tang L;Goldston T;Afriyie-Gyawu E;Lovett C;Griswold J;Brattin B;Taylor RJ;Huebner HJ;Phillips TD; “Short-Term Safety Evaluation of Processed Calcium Montmorillonite Clay (NovaSil) in Humans.” Food Additives and Contaminants, U.S. National Library of Medicine, SOURCE. 
29. Yang, Hsin-Ling, et al. “Humic Acid Induces Apoptosis in Human Premyelocytic Leukemia HL-60 Cells.” Life Sciences, Pergamon, 25 June 2004, SOURCE. 
30. Zhao ZY;Liang L;Fan X;Yu Z;Hotchkiss AT;Wilk BJ;Eliaz I; “The Role of Modified Citrus Pectin as an Effective Chelator of Lead in Children Hospitalized with Toxic Lead Levels.” Alternative Therapies in Health and Medicine, U.S. National Library of Medicine, SOURCE.

Genetics & Mycotoxins: Learn From the Experts

The Great Plains Laboratory has been educating practitioners for over 15 years on how to help patients heal through cutting-edge testing, research and protocols. In our recent 3-Day Environmental Toxin Summit, speakers focused on the epidemics of environmental toxins and pathogen exposure after a foundation of the OAT is presented. Speakers reviewed patient cases and present testing and treatment protocols for toxin and mold-induced illnesses.

The following Q+A is a grouping of responses from a distinguished pool of speakers who participated in the Environmental Toxin Summit with their own unique topics

The material contained within this article is not intended to replace the services and/or medical advice of a licensed healthcare practitioner, nor is it meant to encourage diagnosis and treatment of disease. It is for educational purposes only. Any application of suggestions set forth in the following portions of this article is at the reader's discretion and sole risk. Implementation or experimentation with any supplements, herbs, dietary changes, medications, and/or lifestyle changes, etc., is done so at your sole risk and responsibility.


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MARK FILIDEI, DO

The Hidden Threat of Mycotoxins

Dr. Mark Filidei is an Internal Medicine physician who completed training in General Internal Medicine at Brown University. He is the Director of Integrative Medicine for the Amen Clinics. Dr. Filidei is an officially trained member of ILADS and treats Lyme disease and mold illness with both natural and conventional treatments. He specializes in Hormone Replacement Therapy and the treatment of Mental Health disorders.

Q: Do you see these mycotoxins eliminated with binders on follow up? What do you suggest for patients with constipation?

A: Yes. Plenty of fluids, and magnesium powder if needed.

Q: Has the level and/or distribution of mold and mycotoxins in food changed with climate changes and soil depletion?

A: I do not know, but it would not surprise me at all if that was the case.

Q: What is an example of nasal anti-fungals?

A: Nystatin, itraconazole (compounding pharmacy)

Q: Have you seen any good data with foot detox?

A: No. None. I keep asking them to provide some.

Q: Antifungal nasal spray, more info?

A: Comounding pharmacies like hopkinton do this.

Q: What is your rx for high Citrin levels? What are your main concerns about this?

A: Nothing special for that mycotoxin. Same treatment protocols.

Q: Are you treating with antifungals orally?

A: Yes, when indicated.

Q: After you have remediated and taken binders when do you treat with anti fungal?

A: When there is evidence/concern for systemic mold/yeast.

Q: After you remediate and take binders when you treat with antifungals. what is the rtinale for the various medications?

A: Fluconazole has a lot of resistance so not used often, voriconazole has cns penetration if indicated.

Register now for our upcoming events and workshops.


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Ben Lynch, ND

Genetics and the Impact of Environmental Exposures

Dr. Ben Lynch is the best-selling author of Dirty Genes and President of Seeking Health, a company that helps educate both the public and health professionals on how to overcome genetic dysfunction. He received his doctorate in naturopathic medicine from Bastyr University. He lives in Seattle, WA with his wife and three sons.

Q: Will StrateGene be available in Canada?

A: StrateGene is available internationally and NY via 23andme and Ancestry raw data. Rules and regulations prevent us from offering the StrateGene DNA Kit internationally and in NY. There are many rules surrounding the export of DNA material.

Q: When it says increased copper, are we talking about the relative levels or absolute?  Zn and Moly possibly generating a relatively different level vs an absolute level of copper that may be higher.

A: I do not remember the specifics. We do have a bibliography which will help identify the specifics.

Q: Do you have a pharmacogenetic list in StrateGene?

A: We do not. Pharmacogenetics requires FDA approval. If any genetic reports offer pharmacogenetics without FDA approval, I would steer clear of it due to potential serious misinformation and bad clinical information.

Q: Which air filter do you recommend?

A: I like Alen Air. And here are other products I use and recommend as well:

Q: How do we get this information/reports?

A: There is a lot of education available on strategene.me which requires a login. Access is provided once a test kit is purchased. You may purchase the genetic test HERE.

Q: Cost-effective genetic testing options?

A: Cost-effective or effective? StrateGene is both if you look at the quality of research behind it, the haplotypes offered, detail of epigenetic information on each gene, and the mapping of how genes work together giving you a more comprehensive approach to treatment – and more accurate.

Q: How do we even get started with researching genes for the most conditions that we see?

A: Rephrasing the question is important.

How do we begin understanding the genetic and epigenetic mechanisms of actions behind various conditions so we can better make strategic treatment plans for our patients? StrateGene will help you do it. We have lots of training available in our Education center. The training is included with your purchase of StrateGene.

Q: Can you give some recommendations to dealing with COMT and MAO along with MTHFR genetic deficiencies?

A: In the book, Dirty Genes, I have entire chapters dedicated to each of these genes. I highly recommend picking up that book to give you lots of recommendations, lab testing direction, patient history intake questions, examples and lifestyle, diet, environment and supplement recommendations.

StrateGene also provides this information along with your patient’s specific genetic findings for these genes – including the COMT haplotype which is more clinically relevant than just looking at COMT SNPs alone.

Q: Disulfiram is working against borrelia very well but blocks many Cyp40-enzymes. Any recommendations?

A: Depends on the specific CYP450 enzyme. Anytime supporting Phase 1 detox like CYP450’s, one must be sure to also support Phase 2 and 3 otherwise significant side effects will be created. Sauna is also highly recommended here as that’s fantastic Phase 3 basically.

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Bob Miller, CTN

IL-6, The Good, the Bad and the Ugly

Bob Miller is a Traditional Naturopath specializing in the field of genetic-specific nutrition. He earned his traditional naturopathic degree from Trinity School of Natural Health and is board certified through the ANMA. In 1993, he opened the Tree of Life practice and he has served as a traditional naturopath for 27 years. For the past several years, he has been engaged exclusively with functional nutritional genetic variants and related research, specializing in nutritional support for those with chronic Lyme disease.

Q: How many different protein-coding genes and how many SNP's are tested in the YGR saliva test?

A: 220,000 SNPS.

Q: Can you talk about how Estriol increases IL-6 production?

A: I don’t know the exact mechanism, but if you search for IL-6 and Estriol, the literature will be there.

Q: I am looking into Hyperoxaluria Type 1,2,3. My sons OAT revealed all three markers Oxalic, Glyceric, Glucolic are high. Looks like this test will help clarify the genetic variations, correct?

A: Yes, it looks at several enzymes related to the inability to degrade oxalates.

Q: Is there a particular Gene that causes increased seizures or inability to take or utilize N-Aceytl-Carnitine?

A: Seizure are very complex, and likely not one mutation, but I have observed higher seizure activity when there are NQO1 mutations.

SLC22A5 is the carnitine transporter. Mutations here may make carnitine transportation more difficult.

Q: So for MCAS patients, anxiety and COMT variants, quercetin can worsen anxiety?

A: Yes, as Quercetin may inhibit comment.

I have seen poor response to quercetin.  Interesting - I just looked this patient up and there are many COMT mutations.  Thanks.

Glad that was helpful.

Q: Can you please go over oxidized glutathione inhibiting sulfation. When you take liposomal GSH, what form are you getting?

A: Liposomal to the best of my knowledge, is reduced. I am not aware of the mechanism, but oxidized glutathione inhibits the SULT enzyme, which is responsible for sulfation.

Q: Do the ATG13 mutations up or downregulate?

A: We have not seen any literature on this yet.

Q: This patient's family ages very slowly and has multiple homogenous mutations ATG13 - so would that indicate upregulation?

A: It’s really hard to know, as there are so many variables that could impact aging.

Q: Diamine Oxidase /DAO is another alias for ABP1 gene. Its approved name is AOC1: Amine Oxidase Copper Containing 1.

A: Unfortunately DAO is also an alias for D-Amino Acid Oxidase…which indeed does not break down histamine. It is a perfect storm of bad naming convention.

Yes, it is and confused often.

Q: Sometimes I see that giving Magnolia actually aggravates a person's sleep or doesn't help at all or stops working after a while.  Is there a pathway that would explain this?

A: I’ve seen this on rare occasions and don’t know why it happens.

Q: Given how many variants people have, I am concerned they will be needing to take too many supplements and that has its own issues. How can we decrease how many multi-ingredient supplements in our chronically ill patients with lots of pertinent genetic variances?

A: That’s a common problem with no easy answer. A good rule of thumb is to start with decreasing inflammation first.

Q: For mitigation of EMF effects do you need to take a combination of the Magnesium, K2, Resveratrol etc or take one of item listed individually?

A: A combination is best, check out the product EMF Support at www.functionalgenomicnutirtion.com.

Q: Any thoughts on elevated LDL particle number in patients with mold, Lyme, and MCAS? Could elevated IL-6 be an issue mediating elevated Lipids?

A: It’s quite possible, but really can’t say for sure.

Q: Can you say something about IL-18?

A: We have not researched this yet.

Q: Recommended testing for Hyperoxularia 1,2,3?

A: GPL Organic Acids Test.

Q: Can you do blood or urine tests for Il 6 or Il 8?

A: Blood tests, but it is cyclical during the day, and may be high in the tissue and not the blood.

Q: What was the product you referred to regarding GABA?

A: Excito Blox Clarity.

Contact Yvonne at director@tolhealth.com for information on how to order.

Q: Does your software support 23andme?

A: Yes, but the newer V5 has very limited data.


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Elena Villanueva, DC

Mycotoxins: Considerations, Case Studies and Protocols

Elena Villanueva is an internationally recognized health coach and crusader for ending the global mental health crisis and educating the public and other health professionals that mental health conditions are actually ‘brain health’ issues and when the underlying causes are found, the brain health conditions can be reversed.

Q: My problem is what to do with these test results?

A: Yes, this can be confusing if you don’t understand what to do with the results. 

The reason for ordering the mycotoxin and chemical toxins testing is to see if an individual has any of these toxins. These toxins in general all cause central nervous system dysfunction, GI dysfunction, immune system imbalances, inflammation, oxidative stress, kidney, and liver stress. As you research and learn more about the issues these various toxins because you will get a better understanding of why you want to test for these toxins in the first place. 

I would recommend you sign up for the GPL clinician courses and really dig into those to learn and get confident in how to use protocols, what to expect, etc. when working with these clients. 

We also offer a program that teaches our protocols and our approaches like how to identify ALL the underlying causes of disease and health conditions, realistic timeline expectations, frequency of re ordering labs and what to look for on the lab re orders, what protocols we use, how to trouble shoot, etc.

Q: Why do some patients get really constipated with addition of vitamin k?

A: If the patient is having issues with increased constipation with Vit K being added to their supplement regimen, it is most likely they already have dysbiosis to start with and most likely they already had or were borderline constipated before they started. A healthy gut microbiome will have bacteria that will naturally produce vitamin k. 

 It will be a good idea to find out what was going on with their gut, as a baseline, before you started adding the vitamin K…the constipation issues should be transient and supporting the gut motility while you are working with the patient may be necessary  for a short period of time.

Q: What coffee are you using for your coffee enemas? Wilson's is supposed to be mold free, but I question this based on MycoTOX testing.

A: We use Aussie Co which comes not only with a great quality coffee for the enema but also the entire coffee enema kit. Here is the link if you want to check them out.

Q: I notice you continue to say “client” how are you able to order tests across state line? Do you have a license in more than one state?

A: Good question. We have moved from a doctor-patient relationship with our patients over to a coaching relationship with them. We did this about 3 years ago. We now teach and coach our clients to understand and interpret their own labs and to learn how to use protocols to address their own issues. We can order labs because we are licensed practitioners.

We have chosen to educate our clients rather than ‘treat’ patients because we feel the ‘treatment’ approach is outdated and not sustainable. Yes, some of my coaches including myself are licensed in more than one state. Depending on the lab company you use, they have work - arounds for being able to order labs for client’s or patients that are in another state from where you practice… it just depends on your state rules too, and what license you have, and how you are approaching your work… i.e. are you a doctor or a coach? You will want to check with your state and scope of practice to be sure.

Q: The 65-year-old with heavy long periods - did she have endometrial biopsies?

A: I do not recall that client having heavy long periods at 65. I would have to go back and look at that again, but I am pretty sure that was not one of her issues.

Q: Is the tinnitus referred to in patients the ringing or the pulsatile kind? Provided there is no vascular abnormality could mycotoxins cause or contribute to pulsatile tinnitus?

A: This is usually caused by an infection or inflammation of the middle ear or the accumulation of fluid there. Because infection /inflammation could be an underlying cause I would say that yes, mycotoxins or even heavy metals or chemical toxins could be an underlying cause -- because they DO cause inflammation in the body and can allow for co infections to occur as well.

Q: What was the kidney liver support you used?

A: The KL support from Cellcore. There are also others that work quite well like brands from Designs for Health to Standard Process, to Apex…so the exact one I use doesn’t have to be used. Because we see large volume of clients, we streamline our processes and use the Cellcore brand the most for the detox part of our protocols.

Q: What is your favorite biofilm buster - is it Interfase or Interfase plus or the CellCore products?

A: The Interfase and I. Plus are great, and we use those as well, in addition to the cellcore products, especially if we see in their history clues that lead us to believe they may have a lot of biofilm build up. Coffee enemas are also great at busting up biofilm.

Q: Explain Para 1, Para 2, para 3

A: Para 1 is mimosa pudica, which is a gelatenous, sticky type of plant that ‘grabs’ onto biofilm and parasites in the intestines. It is kind of like a ‘sticky tape’ that grabs on to the biofilm and carries out in the stool. 

Para 2 has ingredients in it that are anti-microbial

Para 3 also has ingredients in it that are antimicrobial and it is much stronger than the Para 2. 

You can go onto the Cellcore biosciences website to check out their products. 

I’m also happy to do an intro email to them if you’d like. My email is drv@modernholistichealth.com. If you want to email me I can do an intro email to any of you who are interested. Please do not put me on any email list!

Q: What do you suggest as the most effective way to address patients emotional issues?

A: The most effective way to address their emotional issues is to start with a good history and some baseline labs like the mycotoxin, heavy metals, chemical toxins, and OAT test, as well as an IgG food sensitivity test. These initial tests can reveal if any of these could be triggers affecting one’s mood, emotions, and brain chemistry. If any of these are found to be underlying causes, then these issues need to be addressed - to remove the barriers to healing. 

You will also want to find out if there are any other triggers like trauma, PTSD, or other heightened emotional experiences that have happened in their lifetime, in utero, or even in previous generations as traumas can be passed down in their genes. These can also be barriers to healing. You will also want to find out what their current situation is… i.e., are they in a stressful environment with their job, relationship, etc. These are all underlying causes that cannot be tested for like toxins but are a huge underlying factor in emotional disturbances and mental health issues and these need to be addressed. And they can be addressed very effectively. We teach trauma work in our certification courses if you are interested.

Q: Would a liver cleanse be helpful during the protocol? If so, when?

A: Yes, it would be. Between the dietary changes we make with our clients and the first month of detox we do with them, they get a good liver cleanse in the beginning of their program. The Standard Process 21 Day cleanse or 28 day are both great to detox the liver and reduce inflammation. I have seen huge decreased in liver enzymes with their detoxes in just a month (using before and after blood labs to see the changes). Also, even if you do not do that, the cellcore protocols will also detox the liver as well.

Q: Can you elaborate on Coffee enemas? Why and how?

A: Coffee enemas are great for stimulating the liver to dump glutathione and produce more of it. It gets absorbed through the hepatic portal vein and goes into the liver. It works great for detoxing, breaking up biofilm, and inflammation reduction.

Q: What brand nebulizer do you recommend?

A: There are many brands that work well. So, I don’t stick to a particular one. I will say that I prefer that one use the face mask attachment rather than just the mouthpiece because we want the C. Silver to also get up into the sinuses… btw, this also works great for sinus infections.

Q: Colloidal silver burns in the nose- how do you buffer since it can't be in saline.

A: Which colloidal silver are you using? The Argentyn shouldn’t burn the nose. I have never had anyone say that when they are using the Argentyn. Also, you can add distilled water to the C Silver to dilute it. 

Q: Would nebulized propolis be helpful in the protocol? If so, when?

A: I am not familiar with nebulized propolis.


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