Mestinon Clinical Trial

  • Wenzhong Xiao, PhD
  • Peng Li, PhD
  • David Systrom, MD
  • Ron Tompkins, MD/ScD (passed away in 2022)
  • There is an enhanced pro-inflammatory cytokine response between the pulmonary and radial arteries in ME/CFS patients compared to symptomatic controls.
  • Plasma proteomics analyses revealed that ~170 proteins were significantly changed in ME/CFS patients compared to controls. Key proteins involved in inflammation, cellular energy metabolism, and Vitamin B12 deficiency were identified.
  • Performing comparison analyses with results from other studies in ME/CFS and Long COVID and with organ aging data.
  • A manuscript is in preparation.

STUDY HYPOTHESIS AND DESCRIPTION

Dr. Systrom has consistently found that some people with ME/CFS suffering from fatigue have Preload Failure (PLF). In this instance, PLF is thought to come from an imbalance in the autonomic nervous system and results in reduced filling of the heart during exertion.

Prior studies have shown that treatment with Mestinon results in symptomatic improvement in patients with PLF. Dr. Systrom intends to evaluate the short-term effects of Mestinon on the autonomic nervous system and neurovascular control in people with ME/CFS with PLF. Studying these features will improve our understanding of ME/CFS and this trial may lead to new therapeutic options for some people with ME/CFS.

More details of this trial can be found here.

OBJECTIVES

David M. Systrom, MD, seated in his office.

  1. Select potential candidates for the study.
  2. Enroll subjects and conduct evaluation at Brigham and Women’s Hospital.
  3. Assign subjects in a 1:1 ratio to receive a 60 mg dose of oral pyridostigmine or placebo after an invasive cardiopulmonary exercise test (iCPET). Perform a second iCPET was 50 minutes later.
  4. Conduct biostatistical analysis to assess:
    • the difference in peak exercise oxygen uptake (VO2)
    • exercise pulmonary and systemic hemodynamics and gas exchange.