Stress-Induced Transcriptomic Changes in Females with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Reveal Disrupted Immune Signatures

Author:

Van Booven Derek J.1ORCID,Gamer Jackson23,Joseph Andrew23,Perez Melanie23,Zarnowski Oskar23,Pandya Meha45,Collado Fanny67,Klimas Nancy26,Oltra Elisa8ORCID,Nathanson Lubov2ORCID

Affiliation:

1. John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL 33136, USA

2. Institute for Neuro-Immune Medicine, Dr. Kiran C. Patel College of Osteopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL 33328, USA

3. Dr. Kiran C. Patel College of Osteopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL 33328, USA

4. Halmos College of Arts and Sciences, Nova Southeastern University, Fort Lauderdale, FL 33328, USA

5. Farquhar Honors College, Nova Southeastern University, Fort Lauderdale, FL 33328, USA

6. Department of Veterans Affairs, Miami VA Healthcare System, Research Service, Miami, FL 33125, USA

7. South Florida Veterans Affairs Foundation for Research and Education Inc., Fort Lauderdale, FL 33125, USA

8. School of Medicine, Universidad Católica de Valencia San Vicente Mártir, 46001 Valencia, Spain

Abstract

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a chronic, complex multi-organ illness characterized by unexplained debilitating fatigue and post-exertional malaise (PEM), which is defined as a worsening of symptoms following even minor physical or mental exertion. Our study aimed to evaluate transcriptomic changes in ME/CFS female patients undergoing an exercise challenge intended to precipitate PEM. Our time points (baseline before exercise challenge, the point of maximal exertion, and after an exercise challenge) allowed for the exploration of the transcriptomic response to exercise and recovery in female patients with ME/CFS, as compared to healthy controls (HCs). Under maximal exertion, ME/CFS patients did not show significant changes in gene expression, while HCs demonstrated altered functional gene networks related to signaling and integral functions of their immune cells. During the recovery period (commonly during onset of PEM), female ME/CFS patients showed dysregulated immune signaling pathways and dysfunctional cellular responses to stress. The unique functional pathways identified provide a foundation for future research efforts into the disease, as well as for potential targeted treatment options.

Funder

NIH

Nova Southeastern University

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference72 articles.

1. Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Essentials of Diagnosis and Management;Bateman;Mayo Clin. Proc.,2021

2. (2015). Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Redefining an Illness, The National Academies Collection: Reports funded by National Institutes of Health; National Institutes of Health.

3. Review of case definitions for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS);Lim;J. Transl. Med.,2020

4. Immune and hemorheological changes in chronic fatigue syndrome;Brenu;J. Transl. Med.,2010

5. Neuroendocrine correlates of chronic fatigue syndrome: A brief review;Demitrack;J. Psychiatr. Res.,1997

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