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LYME Voice - 103 Inflammatory Mechanisms And Biomarkers In The Chronic Manifestations of Lyme Disease-Alaedini, Armin

103 Inflammatory Mechanisms And Biomarkers In The Chronic Manifestations of Lyme Disease-Alaedini, Armin

LYME Voice

05/13/20 • 72 min

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Ep.103

Dr. Armin Alaedini is a professor at Columbia University, where he leads a research laboratory focused on studying the role of the immune system, host-microbe interaction, and diet in complex disorders. His team’s research on Lyme disease in the past 15 years has focused on the chronic and post-treatment manifestations of the infection, leading to seminal findings that provide molecular evidence of a biological basis for the patient’s symptoms. He is currently a member of the Scientific Advisory Board of Global Lyme Alliance and a Working Group Member of the NIH Advisory Council on Chronic Fatigue Syndrome.

Key Takeaways:

  • How does inflammation become permanent?
  • Could there be abnormalities in the immune response system because of Lyme disease?
  • Could there be a biological basis for persistent inflammation?
  • There is a biological basis for the symptoms Lyme patients are facing. This is not trivial, because there wasn’t scientific evidence to say it wasn’t psychosomatic.
  • The infection causes inflammation. Inflammation then becomes chronic.
  • Why do some patients recover and others don’t?
  • Remove the infection, and then you still have to remove the inflammation. Borrelia components could remain.
  • Even after treatment with antibiotics, you can still have Borrelia in the body. (Animal studies)
  • The inflammation that patients have early on in the infection is different than the persistent inflammation that patients have in the later stages of infection. (12:00)
  • Biological markers to demonstrate that patients have chronic persistence of inflammation. This is really important because it gives us a handle to study these patients.
  • There is basically no federal funding for Lyme disease. The NIH gives out a minuscule amount of funding for Lyme disease. Lack of funding is a major reason we haven’t made strides.
  • We know a lot about Borrelia (about the infection itself) but the chronic symptoms that persist after having Lyme disease haven’t been properly studied.
  • We need more support from the NIH and other federal agencies.
  • Chronic Fatigue Syndrome (working group that counsels the NIH)
  • NIH is slowly starting to be more supportive of research around CFS.
  • CFS is a heterogeneous condition. It’s a spectrum disorder, making it very hard to study.
  • There is now a study section at the NIH dedicated to studying CFS.
  • We need funding to entice new researchers in these underfunded areas.
  • Testing for Lyme that is “accepted” as mainstream relies on the immune response to the infection itself.
  • We need to be able to find biomarkers in patients early on in the infection and later post-treatment Lyme disease syndrome. (30:00)
  • We are still at the early stages of understanding (funding, research, clinical trials) these persistent symptoms.
  • We can’t focus only on antibiotics and antibacterial agents. (We need to think more broadly about treatment strategies)
  • Borrelia moves out of the bloodstream very quickly. From the blood, it goes to joints, nervous system and organs.
  • Clinicians and researchers process the information that they have differently.
  • There is a very real psychological toll of unresolved symptoms on the patients.
  • The GUT has its own immune system and nervous system. (53:00)
  • Neuroimmunology-The role of the immune system in neurologic and psychiatric symptoms.
  • The gut interacts heavily with the brain.
  • “I was initially interested in Lyme disease because the laboratory I was working in became interested in patients who were basically experiencing symptoms in response to vaccination from Lyme disease back in the 90’s.” LYMErix
  • There is currently no vaccine for Lyme disease.
  • The early research that I did indicated that there may be some cross-reactivity of the immune response to the vaccine, against the nervous system. That was early research that we did, that we didn’t continue with for lack of funding.
  • What will treatment look like in the year 2040 for Lyme disease? Quick diagnosis, treatment, and resolution of symptoms. Better diagnostics and treatment for various symptoms.
  • The microbiome is a huge factor in health and recovery. (a.k.a diet)
  • Patients are trying everything because that is what they have to do.
  • “60%-70% of chronic fatigue syndrome patients also have gastrin intestinal symptoms. Which is significantly higher than the general population.” (1:02)

Connect with my guest: Dr. Armin Alaedini

Columbia University Institute of Human Nutrition-

630 West 168 Street

PH1512E, New York, NY 10032

  • 212-305-4808

https://www.ihn.cumc.columbia.edu/profile/ar...

05/13/20 • 72 min

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