Dr. Jordan Peterson introduces Dr. Richie Shoemaker and Dr. Scott McMahon, experts in chronic inflammatory response syndrome (CIRS).
CIRS is linked to conditions like sick building syndrome, fibromyalgia, chronic fatigue syndrome, Alzheimer's, and other degenerative neurological conditions.
Exposure to biotoxins in water-damaged buildings, especially those with anti-fungal paints, can trigger an immunological response with various neurological and behavioral consequences.
The military faces a particular problem with low-grade military housing often suffering from water damage and mold infestation.
Dr. Shoemaker explains CIRS and its widespread prevalence.
Over 95% of CIRS patients have defective antigen processing, leading to reduced or absent antibody production.
CIRS involves both inflammation and metabolic abnormalities, resulting in molecular hypometabolism in 95% of chronic fatigue patients.
Genetic mechanisms underlie defective antigen presentation and inflammation, and therapies have been developed to correct gene activation and suppression.
CIRS research aims to correct dieback central nervous system degeneration, including conditions like Alzheimer's, Parkinson's, and ALS.
Dr. McMahon discusses the link between CIRS and living in water-damaged buildings.
Inhalation of microbial growth from molds, bacteria, or actinobacteria triggers the innate immune system, leading to overproduction of cytokines and symptoms similar to the flu.
What percentage of buildings are affected? (11m18s)
Many buildings harbor airborne pathogens, with mold being the most common, especially in water-damaged buildings.
Chronic exposure to these pathogens can trigger an immune response, leading to flu-like symptoms, pain, and chronic inflammation in susceptible individuals.
The percentage of affected buildings in North America and worldwide is significant, with estimates ranging from 50% to 85% according to the United States Environmental Protection Agency (EPA).
Water intrusion is a common factor in affected buildings.
How natural selection created super toxins (17m55s)
Natural selection favored molds and other biohazards that could tolerate exposure to antifungal chemicals in paints and sealants.
As a result, these organisms became more toxic in order to survive, producing more potent toxins.
Fungi respond to environmental hazards by activating genes that produce toxins for predation, not defense.
Actino bacteria thrive in alkaline environments created by substances that kill fungi, changing the pH of drywall over time.
Different groups of fungi and bacteria colonize water-damaged buildings at different stages, depending on the water saturation level.
Certain architectural features make buildings more likely to become water damaged, such as flat roofs, basements, and crawl spaces.
Drywall is more prone to problems compared to plaster on lathe.
The widespread use of drywall in the latter half of the 20th century, combined with the use of fungicides in paints, has contributed to the contamination of a significant number of buildings.
What level of contamination constitutes a critical issue? (22m48s)
Individual susceptibility plays a crucial role in determining who gets sick from exposure to contaminated buildings.
Studies have shown that around 95% of individuals with a specific immune response gene (HLA-DR) develop symptoms when exposed to contaminated environments.
Long COVID and chronic inflammatory and metabolic response syndrome can be triggered by an initial priming event, such as COVID-19 infection, in individuals living in contaminated buildings.
Common illnesses and conditions that may actually be CIRS (56m52s)
CIRS may be associated with a higher risk of Alzheimer's in Finland due to architectural designs that make houses more susceptible to biotoxins.
CIRS symptoms can be detected decades before Alzheimer's develops, as seen in studies of nuns' writing samples.
Verbal fluency tests may be useful markers for cognitive interference in CIRS.
CIRS can cause various neurological degenerative conditions, including tremors, metallic taste, dizziness, vertigo, and cognitive deficits.
Neuroquant, a brain imaging technique, can detect abnormalities in CIRS patients and can be used to monitor treatment progress.
Different patterns of brain damage are associated with CIRS caused by water-damaged buildings (enlarged forebrain parenchyma, enlarged cortical gray matter, and atrophied caudate nucleus) and Lyme disease (enlarged putamen and atrophied caudate nucleus).
VIP (vasoactive intestinal polypeptide) therapy has been shown to stop or reverse caudate nucleus and multinuclear atrophy in CIRS patients.
Leptin resistance, associated with obesity, can lead to decreased production of MSH, resulting in fatigue, pain, and weight gain.
CIRS can contribute to obesity through molecular hypometabolism and weight storage mechanisms.
Research has found that activating brown fat and increasing energy consumption can help combat weight storage and fat storage.
The GOV found their research credible, then ignored them (1h22m38s)
The researchers presented their findings to the House and Senate Armed Services Committee, resulting in a $300 million appropriation for investigating military housing.
The report highlighted the presence of mold and infestations in military housing, potentially affecting troop readiness and the mental and physical health of service members and their families.
25% of people are susceptible to CIRS due to physiological and genetic reasons.
Genetic markers can indicate susceptibility to CIRS.
Ribosomes, the structures that make proteins, can be affected by toxins, leading to impaired protein production and cell dysfunction.
Mitochondrial dysfunction occurs, with glucose being broken down into lactic acid instead of being used for energy production.
Metabolic acidosis, lack of regulatory T cells, gray matter nuclear atrophy, pulmonary hypertension, obesity, and insulin resistance are complications of metabolic abnormalities.
Insulin receptor substrate 2 (IRS2) can affect glucose uptake and metabolism, impacting the effectiveness of diets like the keto diet and the carnivore diet.
Defective apoptosis (programmed cell death) leads to an increased antigen load in the bloodstream, contributing to inflammation.
Genetic markers associated with defective apoptosis, such as RPK1, can indicate an endogenous source of CIRS.
Upregulation of coagulation factors can bind to TA and T beta in the brain, creating microclots and contributing to Alzheimer's disease.
Increased cytokines and specific markers for endotoxins, such as TGFBR1 and MAP3K8, indicate actinobacteria injury.