What is Chronic Inflammatory Response Syndrome (CIRS)?

 

Chronic Inflammatory Response Syndrome (CIRS) is a multisystem, multi-symptom illness triggered by biotoxin exposure. A biotoxin is any living toxin. When exposed, the immune system can become stuck in an inflammatory state even when the exposure is removed.

 

24% of the population is genetically at risk to develop CIRS, due to alterations in their Human Leukocyte Antigen genes (HLA). There are specific HLA genes involved in CIRS and you only need to have one gene to be predisposed. For those genetically at risk for CIRS, chronic exposure to external infections, toxins, or inflammatory signals from within the body causes an ongoing innate immune response in the immune system.

 

The innate immune system, which is the non-specific first line of immune defense, turns on, as it should in response to any exposure. However, having one or more of the HLA genes will prevent a handover to the adaptive immune system. This means there is no antibody created and the innate immune system is never told to shutoff. As a result cytokines, the proteins produced by the immune system are over produced, and inflammation is triggered, regardless of whether the exposure is still there or not.

 

You have these genes your whole life, but they are only expressed when you have a combination of biotoxin exposures (one or many) and other stresses on the system, such as toxin exposures, stress, and food triggers. These environmental inputs will trigger the gene expression at different times – you can first be diagnosed as a child, or in your later years.

 

This dysregulation and inflammation can lead to damaged tissues and cells, alter gene expression, autoimmunity, and disrupt hypothalamic hormones (hormones produced in the brain), downstream hormones (hormones downstream from the brain), and peptides (small chains of amino acids). This causes many debilitating symptoms, which can affect every body system. Chronic Inflammatory Response Syndrome is a progressive illness that if left untreated can rob patients of their quality of life.

 

Triggers of Chronic Inflammatory Response Syndrome

 

CIRS is the result of downstream abnormalities that occur in the body from biotoxin exposure. A biotoxin is a toxic substance produced by living organisms.

 

A patient may be exposed to biotoxins from the mold and bacteria in water-damaged buildings, from diseases caused by tick bites, by consuming tropical fish, or even exposure to certain algae.

 

Knowing whether your Chronic Inflammatory Response Syndrome trigger is current is critical for proper recovery. That is why it is so important for physicians to get a thorough history from you before diagnosing or treating CIRS. In some cases we may not be able to figure out the exact trigger (or when it occurred), but we are most interested in ruling out current external exposures and internal infections.

 

CIRS triggers can be from any of the following:

 

  • Microbes, toxins and inflammagens from Water Damaged Buildings (WDB). The main 3 are mold, actinobacteria and endotoxin. We typically test for these inside the home.
  • Lyme disease and co-infections
  • Cyanobacteria (blue grey algae), often from freshwater exposures such as lakes
  • Apicomplexans like Babesia (parasite)
  • Pfiesteria, from exposure to ill fish – swimming
  • Ciguatera, from eating tropical fish
  • Red tide
  • Recluse spider bites
  • Mycobacteria
  • Traumatic brain injury can trigger similar downstream effects as CIRS

 

Symptoms of CIRS

 

Due to varied environmental stimuli and each individual’s unique genes, patients with Chronic Inflammatory Response Syndrome can present with wildly different symptoms. Because of the wide range of symptoms a CIRS diagnosis can be easily missed at family doctor visits, mostly because it is not looked for. Patients with CIRS are often misdiagnosed with allergies, anxiety, depression, PTSD, Alzheimer’s, Parkinsonism, Chronic Fatigue Syndrome, and many other conditions.

 

When CIRS is suspected, an easy screening symptom questionnaire & visual contrast sensitivity test can accurately delineate who may be at risk. This will then alert us to test further. Our Functional Medicine Physicians at Linden & Arc get to the root cause of your symptoms, so you can be sure you are receiving proper treatment.

 

CIRS is often suspected if:

 

  1. You have a complex multi system, multi symptom illness.
  2. You are not responding as expected to basic treatments, such as gut, hormone and nutrient treatments.
  3. You have atypical presentation of illness that may not necessarily fit into a clear diagnostic box in the conventional medical system
  4. You have multiple chemical sensitivities
  5. You have a known infective exposure, or home exposure

 

CIRS Symptoms:

 

  • Abdominal pain/diarrhea
  • Disorientation/confusion
  • Teary eyes
  • Metallic taste
  • Congested sinuses
  • Shortness of breath
  • Memory loss
  • Body aches/weakness
  • Headache/light Sensitivity
  • Brain fog/ difficulty concentrating
  • Skin sensitivities
  • Red eyes/blurred vision
  • Mood swings
  • Joint pain/cramps/stiffness
  • Numbness
  • Fatigue
  • Vertigo
  • Excessive thirst
  • Cough
  • Difficulty regulating body temperature
  • Increased urinary frequency
  • Appetite changes

 

Many Patients struggling with Chronic Inflammatory Response Syndrome may also deal with:

 

  • Histamine issues and Mast Cell Activation Syndrome (MCAS)
  • Electromagnetic / EMF sensitivity
  • Limbic system dysfunction
  • Over reactive nervous system (from Neuroinflammation)
  • Poor detoxification
  • Issues with gut health, hormones, nutrient imbalances, neurotransmitter imbalances

 

As discussed, CIRS is an inflammatory illness. However, we also now know that it causes significant disruption in the metabolism of the cell, including energy and protein production. It has transcriptomic effects, meaning it can also turn genes on and off. We see a specific pattern of gene dysregulation in CIRS at baseline, vs. after treatment. This is an extremely important part of correcting CIRS, as our goal is to prevent some of the complications that occur as a result of gene dysregulation.

 

Complications of Gene dysregulation include:

 

  • Insulin dysregulation
  • Metabolic acidosis
  • Low metabolism and energy production
  • Low protein production
  • Pulmonary hypertension
  • Effects on brain structure/ volume

 

Chronic Inflammatory Response Syndrome Diagnosis

 

The presentation of Chronic Inflammatory Response Syndrome varies between different people. That is why it is extremely important to have a thorough workup done when you are suffering with a wide range of symptoms. An in depth history of your entire ‘timeline”, your life story, your exposure history, and detailed lab investigations are needed. The various tests are necessary for a firm CIRS diagnosis and to properly track the success of treatments. We want to be sure we are on the right track and that you are responding to treatment and will continuously trouble shoot your individual illness. In complex illness, there is no room for guessing!

 

At Linden & Arc Vitality Institute the following Testing is done at baseline and repeatedly throughout the protocol:

 

1. Proteomic Lab Testing

 

Proteomic testing is how we make the diagnosis of CIRS, as per published literature. Below is a list of the labs, with short description of what they indicate:

 

  • Visual contrast sensitivity (VCS) test – this is an eye test measuring contrast, which decreases in people with CIRS
  • HLA testing tells us about your susceptibility to CIRS – are you one of the 24% of people with defective antigen presentation?
  • MSH – melanocyte stimulating hormone, is a key regulator of many important body functions
  • Capillary hypoperfusion: VEGF
  • Innate Inflammatory markers: MMP 9, C4a, C3a and TGF beta 1
  • Disruption of hormone feedback loops: ACTH/ cortisol; ADH or Copeptin/osmolality
  • Androgens and sex hormones
  • Leptin (leptin resistance)
  • Autoimmunity: Antigliadin antibodies and anti-cardiolipin antibodies
  • Abnormal clotting profiles: PAI I; vWF; D dimer; ESR
  • MARCONS nasal swabbing, for a resistant bacteria that sits in the sinus

 

2. GENIE (Genetic Expression, Inflammation Explained)

 

GENIE is a study of the transcriptome developed by James Ryan PhD at ProgeneX labs. Transcriptomic testing tells us how your genes are being expressed in response to environmental inputs. GENIE can tell us about your exposures, hypometabolism and insulin signaling, VIP (Vaso-Active Intestinal Peptide) and Ikaros function, coagulation risks, histamine production, brain and cognitive risks, and confirm a CIRS diagnosis. This test has proven to give us absolutely astonishing insights into your individual expression of the complex illness that is CIRS. It is used at baseline and in follow up to ensure resolution of the illness.

 

3. NeuroQuant Volumetric Brain MRI

 

Volumetric brain imaging is extremely useful in diagnosing the cause of CIRS and establishing the effect of CIRS on the brain. The function of the immune system is intricately linked with that of the nervous system, so we expect to see some changes in the brain in CIRS. Unlike a conventional MRI, it measures volumes of different brain areas with tremendous accuracy. The pattern of change in the volumes of different brain structures will vary depending on what the specific trigger is and if we can see a ‘fingerprint’ for CIRS on the brain. The volume changes, for example, will look very different if mold was your trigger, vs. endotoxin vs. Lyme disease. NeuroQuant will help to determine specifics of treatment and what the end point of treatment is for CIRS.

 

The combination of Proteomic labs, GENIE and NeuroQuant leaves us with solid objective data. You will know that you have a diagnosis of CIRS, without question. You will know what your individual trigger is, and you will have a baseline to track changes and evaluate the success of treatment using accurate data.

 

CIRS Treatment

 

Depending on how quickly we remove you from your exposures and how you respond to each treatment, it can take a year or more to show improvements. The goals of Chronic Inflammatory Response Syndrome treatment are to lower inflammagens, correct hormonal dysregulation, deal with autoimmunity, improve capillary hypoperfusion, eradicate commensal Staph in the nasal cavity, correct cellular immunity, and get you back to enjoying your life.

 

Once CIRS is diagnosed we follow the 12-step Shoemaker protocol as the core of therapy. It is important to follow this peer reviewed protocol for success of treatment. We may also suggest completing other therapies, which support your system and help with repair and possible side effects of the treatments. The most important part of the protocol initially is to remove you from the exposure/trigger for CIRS. This might involve referral to an Indoor Environmental Professional (IEP), who is the expert in home health as it relates to CIRS. They will individualize home testing and remediation based on your results and response to treatment. Removing from exposure also includes removing internal exposures, like infections. We treat Lyme and Lyme co-infections, virus, parasites for example, so that there is no ongoing trigger inside the system. This is individualized based on your testing.

 

Once we have ticked this first important box, we can begin to remove biotoxins from the system with binding therapy, which acts like an antibody and removes biotoxin from the system through the stool. The VCS test is used to track readiness for the next step, which is to eradicate MARCONS from the nasal cavity. Once we have done this we are able to assess progress through repeat testing and manage any ongoing inflammation where necessary.

 

The ultimate goal is to get you taking VIP, which is an important peptide used to calm inflammation, correct gene dysregulation and correct the brain changes associated with CIRS, amongst many other important functions. Management of other related issues and differential diagnoses occur alongside this core approach where needed. For example, Mast Cell Activation Syndrome can be treated, EMF remediation done and detoxification supported.

 

We have a strong focus on the limbic system, which is our emotional brain, as this is commonly an area affected by CIRS. In fact, many patients with CIRS suffer concomitantly with PTSD and other trauma related issues. As the brain-immune connection is so strong, it is important to manage both of these side by side.

 

We find the most successful healing journeys embrace a team approach that includes Indoor Environmental Professionals (IEP), a Health Coach, a Lymphatic Drainage Therapist, and a CIRS literate Physician. At Linden & Arc Vitality Institute, Dr. Murfin is a Chronic Inflammatory Response Syndrome Proficiency Diplomat. We encourage you to ask questions, get support where you can, and to trust that this evidence based treatment plan works, even though it may be challenging.

 

Contact Linden & Arc Vitality Institute

 

At the Institute we understand it can be very overwhelming to deal with the unpredictable and fluctuating symptoms caused by CIRS. That is why we are here to help you every step of the way. It’s time to break the cycle of unnecessary suffering with pro-active treatments that will change the arc of your life.

 

At Linden & Arc we can help you find freedom from pain, fatigue, memory loss, illness, and depression! If you are struggling with persistent health challenges contact us HERE to get started on your transformative health journey.

 

Author

Dr. Michelle Van Der Westhuizen, MD & CIRS Proficiency Diplomat

To understand why we would run certain lab tests, it is important to understand how a person acquires CIRS. First, a genetically susceptible person (more on this later) is exposed to a biotoxin source. The crux of CIRS illness is dysregulated communication between the two arms of the immune system -the innate and adaptive immune system. Normally the innate immune system would flag the biotoxin and present it to the adaptive immune system that would get rid of it and create an antibody towards it for subsequent exposures.

 

However, in CIRS, the adaptive immune system doesn’t recognize the biotoxins the innate immune system is flagging, and this allows the biotoxins to stay in the body creating uncontrolled inflammation that never stops. The ongoing absence of protective antibodies to biotoxins is what causes CIRS. We can measure the immune response to this inflammation through “proteomics” which will be abnormal in almost every CIRS patient. Below are the proteomic labs we most often run at Linden & Arc Vitality Institute: 

 

HLA:

HLA is the biggie. HLA stands for Human Leukocyte Antigen, and these are a set of genes on chromosome 6 that encode proteins that regulate the immune system. HLA lets us know if you are genetically susceptible to inflammation provoked by biotoxins. And not everyone is! Approximately 25% of the population will be susceptible to CIRS. This is the core of why some people get sick, and others don’t – the predisposition is built into the DNA.

 

MSH:

MSH is a hormone made in the pituitary gland in the brain. MSH is the master regulator as it plays an important role in regulating hormones, inflammation, and defence against pathogens. MSH deficiency in CIRS patients is common and can lead to fatigue, chronic pain, insomnia and non-restorative sleep from disrupted circadian rhythms, increased intestinal permeability (IBS like symptoms), sexual dysfunction, and other hormonal irregularities.

 

MARCONS:

Lowered MSH also allows for MARCONS to colonize deep in the nasal sinuses. MARCONS thrives in the biofilm of your nasal mucous membranes and secrete neurotoxic substances into the central nervous system (brain) and worsens the clinical symptoms.

 

TGF beta-1:

TGF beta-1 may be the single most important lab finding. It is pleiotropic meaning it can either suppress or induce inflammation. It plays a key role in controlling the body’s response to biotoxin exposure by regulating immune pathways. Elevated TGF beta-1 indicates there is an overactive immune response occurring, and inflammation has become the dominant response.

 

MMP9:

This is an enzyme that allows inflammatory compounds to leave the blood stream and enter organs and tissues.  This causes widespread inflammation, especially in the lungs, brain, muscles, joints, and nerves.

 

C4a:

This is an inflammatory marker specific to the innate immune system – the first line of defense to immune threats. C4a is part of that sequence of events that occurs when a pathogen sparks the innate immune system response. High levels of C4a are often seen in CIRS and contributes to shortness of breath, fatigue, brain fog, and dysfunction in thinking and memory.

 

VEGF:

Vascular Endothelial Growth Factor is a protein that stimulates the growth of new blood vessels to increase oxygen supply to tissues when circulation is reduced. In CIRS, VEGF is usually low from inflammatory cytokines, and this leads to poor oxygen delivery to muscles. Reduced oxygen leads to cramping and fatigue especially occurring after exercise or physical activity.

 

ACTH/ CORTISOL:

ACTH is a hormone released by the pituitary gland in the brain that tells your adrenals -little hat shaped glands on top of your kidneys – to produce cortisol. ACTH and cortisol are in a delicately balanced feedback system. Cortisol is the steroid hormone responsible for the stress response also known as “fight or flight”.  Cortisol has many other roles including blood sugar balance, immune regulation, as well as response to physical/emotional stress. Chronic stress from ongoing inflammation in prolonged illness causes cortisol production to become dysregulated and this may appear as an inability to handle stress, sleep disturbances, blood sugar imbalances (dizziness, low blood sugar), and fatigue.

 

ADH/ OSMOLALITY:

Anti-diuretic hormone is made in the hypothalamus in the brain and regulates the body’s ability to hold water. Osmolality is the concentration of chemical solutes (sodium, potassium, calcium) that are found in the serum or liquid part of the blood. In CIRS, there is a lack of regulation of the balance of salt and water, and this happens when ADH is low (or too high) and osmolarity is too high (or too low). This will cause dehydration headaches (even migraines), excessive thirst, and frequent urination. With sodium levels increasing in the blood, sweat will also have additional salt in it and this can create increased susceptibility to electric static shocks. This is frequently seen as shocking light switches or seeing blue sparks when you rub your feet against the sheets when in bed. 

 

There is a lot to decipher in complex illnesses like CIRS. At Linden & Arc Vitality Institute, we can help you figure out your diagnosis and determine the best courses of action based on your health needs and case. To book an appointment or for more information, contact [email protected].

 

References

Berndtson, K., McMahon, S., Ackerley, M., Rapaport, S., Gupta, S., & Shoemaker, R.C., (2008). Medically sound investigation and remediation of water-damaged buildings in cases of CIRS-WDB. Retrieved from https://www.survivingmold.com/MEDICAL_CONSENSUS_STATEMENT_10_30_15.PDF

 

Shoemaker, R.C. (2010). Surviving mold: Life in the era of dangerous buildings. Otter Bay Books.

 

Shoemaker, R.C., Andrew, H., Annalaura, M., Ryan, J. (2017). Inflammation induced chronic fatiguing illnesses: A steady march towards understanding mechanisms and identifying new biomarkers and therapies. Internal Medicine Review (3)11, 1-29. 

 

Shoemaker, R.C., Johnson, K., Lysander, J., Berry, Y., Dooley, M., Ryan, J., & McMahon, S. (2018). Diagnostic process for CIRS: A consensus statement report of the Consensus Committee of Surviving Mold. Internal Medicine Review, 4(5), 1-47.

 

Shoemaker, R.C., Mark, L., McMahon, S., Thrasher, J., Grimes, C. (2010). Research Committee Report on diagnosis and treatment of chronic inflammatory response syndrome caused by exposure to the interior environment of water-damaged buildings. Policyholders of America. Retrieved from https://www.survivingmold.com/docs/POA_MOLD_7_27_10_final.pdf

 

Shoemaker, R.C., McMahon, S., & Heyman, A. (2020). The art and science of CIRS medicine. Ebook retrieved from https://www.survivingmold.com/store1/books/art-and-science-of-cirs 

 

Shoemaker, R.C., Neil, V., Heyman, A., van der Westhuizen, M., McMahon, S., & Lark, D. (2001). Newer molecular methods bring new insights into human- and building- health risk assessments from water-damaged buildings: Defining exposure and reactivity, the two sides of causation of CIRS-WDB illness. Medical Research Archives (9)3, 1-36. DOI: https://doi.org/10.18103/mra.v9i3.2358   

 

For more information, go to: https://www.survivingmold.com

 

Author:

Dr. Ayla Lester, ND

Chronic Inflammatory Response Syndrome (CIRS) describes a group of symptoms and specific lab findings associated with biotoxin exposure in genetically susceptible individuals. When your doctor suspects you have CIRS, this is based initially on an eye test (Visual Contrast Sensitivity or VSC) and a set of specific symptoms.

 

The set of specific symptoms are outlined in something called the “CIRS Symptom Cluster Questionnaire” that is usually done on intake and during the first visit – it is that important!  Alongside a skilled medical history, this questionnaire statistically separates CIRS from all other diseases. No other illness to date will have a finding of 8/13 clusters of symptoms present! The likelihood of having a CIRS illness with a score of 8/13 or higher, is 95%!

 

The CIRS Symptom Cluster Questionnaire:

If one symptom or all symptoms are checked off in a category, this counts for one point for the category.

  1. Fatigue, weakness
  2. Headaches
  3. Joint aches, muscle aches, muscle cramps
  4. Unusual sharp, claw, electrical pain or ice pick pain
  5. Light sensitivity, eye redness, blurring of vision, tearing
  6. Shortness of breath, cough, sinus congestion or nasal drainage
  7. Abdominal tenderness or pain, secretory diarrhea
  8. Joint pain, morning stiffness
  9. Executive function difficulty, memory difficulty, poor concentration, difficulty with finding words, confusion, disorientation, difficulty assimilating new knowledge
  10. Mood changes; appetite swings, sweats, poor regulation of temperature
  11. Excessive thirst, frequent urination, static electric shocks
  12. Numbness, tingling, taste disturbance (metallic taste) 
  13. Vertigo, tremor, unusual skin sensations

CIRS

When we add a failed VCS test to a positive Symptom Cluster Questionnaire (8/13 or greater), the likelihood that we are dealing with a CIRS illness is 98.5%. The VCS test tells us if there are visual deficits from biotoxin exposure. Biotoxins are a dangerous mix of chemicals, mold, bacteria, and inflammation provoking compounds in water damaged buildings.

 

Additionally, CIRS can have other triggers such as tick bites (with Lyme disease), brown recluse spider bites, and ingestion of contaminated reef fish. Biotoxins stir up inflammation by provoking immune cells to release cytokines that reduce blood flow to the retina and the optic nerve. The retina is the part of the eyes that enables vision, and the optic nerve is the nerve that carries impulses from the retina to the brain for visual information to be interpreted. With decreased blood flow to these areas, the ability to discriminate contrast is reduced. Contrast is the ability to see an edge/detect a visual pattern. 92% of CIRS patients will have a difficult time distinguishing contrast and will fail the VCS test.

 

There are additional tests that are important to run not only to confirm the diagnosis of CIRS but also for tracking the success of treatments. Clinically, we want you to be symptom free and living your best life, and, from a pathology perspective, we want certain lab markers – proteomics, GENIE, and NeuroQuant- to come back into a normal range. When these lab markers are dysregulated, the organs that get injured from uncontrolled inflammation are the brain, heart, and lungs.

 

At Linden & Arc Vitality Institute, we can help you figure out your diagnosis and determine the best courses of action based on your health needs and case. To book an appointment or for more information, contact [email protected].

 

References

Berndtson, K., McMahon, S., Ackerley, M., Rapaport, S., Gupta, S., & Shoemaker, R.C., (2008). Medically sound investigation and remediation of water-damaged buildings in cases of CIRS-WDB. Retrieved from https://www.survivingmold.com/MEDICAL_CONSENSUS_STATEMENT_10_30_15.PDF

 

Shoemaker, R.C. (2010). Surviving mold: Life in the era of dangerous buildings. Otter Bay Books.

 

Shoemaker, R.C., Andrew, H., Annalaura, M., Ryan, J. (2017). Inflammation induced chronic fatiguing illnesses: A steady march towards understanding mechanisms and identifying new biomarkers and therapies. Internal Medicine Review (3)11, 1-29. 

 

Shoemaker, R.C., Johnson, K., Lysander, J., Berry, Y., Dooley, M., Ryan, J., & McMahon, S. (2018). Diagnostic process for CIRS: A consensus statement report of the Consensus Committee of Surviving Mold. Internal Medicine Review, 4(5), 1-47.

 

Shoemaker, R.C., Mark, L., McMahon, S., Thrasher, J., Grimes, C. (2010). Research Committee Report on diagnosis and treatment of chronic inflammatory response syndrome caused by exposure to the interior environment of water-damaged buildings. Policyholders of America. Retrieved from https://www.survivingmold.com/docs/POA_MOLD_7_27_10_final.pdf

 

Shoemaker, R.C., McMahon, S., & Heyman, A. (2020). The art and science of CIRS medicine. Ebook retrieved from https://www.survivingmold.com/store1/books/art-and-science-of-cirs 

 

Shoemaker, R.C., Neil, V., Heyman, A., van der Westhuizen, M., McMahon, S., & Lark, D. (2001). Newer molecular methods bring new insights into human- and building- health risk assessments from water-damaged buildings: Defining exposure and reactivity, the two sides of causation of CIRS-WDB illness. Medical Research Archives (9)3, 1-36. DOI: https://doi.org/10.18103/mra.v9i3.2358   

 

For more information, go to: https://www.survivingmold.com

 

Author:

Dr. Ayla Lester, ND

This video is a presentation at a CIRS conference – I Dream of GENIE Webinar — CIRSx: Joining the Mission in October 2021. Former physician at Linden & Arc Vitality institute, Dr. Michelle van der Westhuizen, was featured at the conference with Dr. Ritchie Shoemaker and CIRS Academy Faculty.

 

This is the abstract from the video presentation at CIRSx:”PTSD is a prevalent condition, although very underdiagnosed. We now have a transcriptomic (gene expression) marker, called FKBP5 to further assess PTSD and other chronic stressors. The upregulation of this gene tells us that a patient has an altered response to stress and likely limbic system dysregulation. This activated gene may lead to chronic disease and psychiatric conditions down the line. This presentation dives deep into FKBP5 – what is it, how does its activation disrupt our physiology, what illnesses may occur as a result. Also discussed are potential ways for us to manage this. Currently, this marker is only screened for in our CIRS patients, but has promising future applications in mental health and other illness.”

 

Below you can watch the full 30-minute presentation for the CIRSx Conference: