Christopher Larrimore: Difference between revisions
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After matriculation into medical school, he began pursuing ME research on a one-year research fellowship at NSU-KPCOM.<ref name=":0" /> | After matriculation into medical school, he began pursuing ME research on a one-year research fellowship at NSU-KPCOM.<ref name=":0" /> | ||
His current ME research examines genetics and a hypothesized role of 5-MTHF (active [[folate]], methylfolate, or Vitamin B9) in people with ME.<ref name=":0" /> [[Methylation]] is a mechanism central to the functioning of numerous biochemical pathways, including in cardiovascular, neurological, reproductive, energy production and detoxification biochemical systems.<ref name=":0" /> If a genetic variant reducing available 5-MTHFR is present, it reduces the body's ability to activate these systems, possibly producing fatigue such as seen in the clinical presentation of ME.<ref name=":0" /> To examine this possible link to ME, Larrimore used a genetic database developed by Dr. [[Nancy Klimas]]’s team at the NSU [[Institute of Neuro-Immune Medicine]] to identify persons with a MTHFR gene mutation and recruit for a small, proof-of-concept study of the role of folate in ME.<ref name=":0" /> Over three months in a double-blinded study, subjects took either daily methylfolate supplement or a placebo and outcomes were measured both by serum biomarkers and self-reported symptoms. In July 2019, he was awarded a Blue Ribbon Fellowship from [[MEAction]] to continue this project.<ref name=":0" /> | His current ME research examines genetics and a hypothesized role of 5-MTHF (active [[folate]], [[methylfolate]], or [[Vitamin B9]]) in people with ME.<ref name=":0" /> [[Methylation]] is a mechanism central to the functioning of numerous biochemical pathways, including in cardiovascular, neurological, reproductive, energy production and detoxification biochemical systems.<ref name=":0" /> If a genetic variant reducing available 5-MTHFR is present, it reduces the body's ability to activate these systems, possibly producing fatigue such as seen in the clinical presentation of ME.<ref name=":0" /> To examine this possible link to ME, Larrimore used a genetic database developed by Dr. [[Nancy Klimas]]’s team at the NSU [[Institute of Neuro-Immune Medicine]] to identify persons with a MTHFR gene mutation and recruit for a small, proof-of-concept study of the role of folate in ME.<ref name=":0" /> Over three months in a double-blinded study, subjects took either daily methylfolate supplement or a placebo and outcomes were measured both by serum biomarkers and self-reported symptoms. In July 2019, he was awarded a Blue Ribbon Fellowship from [[MEAction]] to continue this project.<ref name=":0" /> | ||
==Publications== | ==Publications== | ||
Revision as of 07:36, July 27, 2019
Christopher Larrimore, BS, MS, is an osteopathic medical student at Nova Southeastern University and conducts research examining the hypothesized role of folate in myalgic encephalomyelitis (ME).
Early life and education[edit | edit source]
Larrimore, who is from Maryland, US, served four years in the US Coast Guard before enrolling in the University of Maryland, where he earned a Bachelor of Science. He next earned a Master in Science from Johns Hopkins University.[1] He next conducted research for two years before beginning medical school at Dr. Kiran C. Patel College of Osteopathic Medicine (NSU-KPCOM) at Nova Southeastern University. In 2019, he begins his fourth year of medical school.[1]
Research[edit | edit source]
On a two-year research fellowship from the Johns Hopkins University, Larrimore investigated blood vessel growth in response to tumor formation.[1]
After matriculation into medical school, he began pursuing ME research on a one-year research fellowship at NSU-KPCOM.[1]
His current ME research examines genetics and a hypothesized role of 5-MTHF (active folate, methylfolate, or Vitamin B9) in people with ME.[1] Methylation is a mechanism central to the functioning of numerous biochemical pathways, including in cardiovascular, neurological, reproductive, energy production and detoxification biochemical systems.[1] If a genetic variant reducing available 5-MTHFR is present, it reduces the body's ability to activate these systems, possibly producing fatigue such as seen in the clinical presentation of ME.[1] To examine this possible link to ME, Larrimore used a genetic database developed by Dr. Nancy Klimas’s team at the NSU Institute of Neuro-Immune Medicine to identify persons with a MTHFR gene mutation and recruit for a small, proof-of-concept study of the role of folate in ME.[1] Over three months in a double-blinded study, subjects took either daily methylfolate supplement or a placebo and outcomes were measured both by serum biomarkers and self-reported symptoms. In July 2019, he was awarded a Blue Ribbon Fellowship from MEAction to continue this project.[1]
Publications[edit | edit source]
- 2019, Understanding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and the Emerging Osteopathic Approach: A Narrative Review.[2]
References[edit | edit source]
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 "Announcing #MEAction's Blue Ribbon Fellow: Investigating the Role of Folate in ME". #MEAction. July 24, 2019. Retrieved July 27, 2019.
- ↑ Larrimore, Christopher; Ramnot, Amanda; Jaghab, Annmarie; Sarduy, Sofia; Guerrero, George; Troccoli, Peter; Hilton, Kelly; Bested, Alison (July 1, 2019). "Understanding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and the Emerging Osteopathic Approach: A Narrative Review". The Journal of the American Osteopathic Association. 119 (7): 446. doi:10.7556/jaoa.2019.081. ISSN 0098-6151.
