Impact of COVID-19 on myalgic encephalomyelitis/chronic fatigue syndrome-like illness prevalence: A cross-sectional survey

PLoS One. 2024 Sep 18;19(9):e0309810. doi: 10.1371/journal.pone.0309810. eCollection 2024.

Abstract

Background: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) can be triggered by infectious agents including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However, the impact of the coronavirus disease 2019 (COVID-19) pandemic on ME/CFS prevalence is not well characterized.

Methods: In this population-based cross-sectional study, we enrolled a stratified random sample of 9,825 adult participants in the Kaiser Permanente Northern California (KPNC) integrated health system from July to October 2022 to assess overall ME/CFS-like illness prevalence and the proportion that were identified following COVID-19 illness. We used medical record and survey data to estimate the prevalence of ME/CFS-like illness based on self-reported symptoms congruent with the 2015 Institute of Medicine ME/CFS criteria. History of COVID-19 was based on a positive SARS-CoV-2 nucleic acid amplification test or ICD-10 diagnosis code in the medical record, or self-report of prior COVID-19 on a survey.

Results: Of 2,745,374 adults in the eligible population, an estimated 45,892 (95% confidence interval [CI]: 32,869, 58,914) or 1.67% (CI 1.20%, 2.15%) had ME/CFS-like illness. Among those with ME/CFS-like illness, an estimated 14.12% (CI 3.64%, 24.6%) developed the illness after COVID-19. Among persons who had COVID-19, those with ME/CFS-like illness after COVID-19 were more likely to be unvaccinated and to have had COVID-19 before June 1, 2021. All persons with ME/CFS-like illness had significant impairment in physical, mental, emotional, social, and occupational functioning compared to persons without ME/CFS-like illness.

Conclusions: In a large, integrated health system, 1.67% of adults had ME/CFS-like illness and 14.12% of all persons with ME/CFS-like illness developed it after COVID-19. Though COVID-19 did not substantially increase ME/CFS-like illness in the KPNC population during the study time period, ME/CFS-like illness nevertheless affects a notable portion of this population and is consistent with estimates of ME/CFS prevalence in other populations. Additional attention is needed to improve awareness, diagnosis, and treatment of ME/CFS.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • COVID-19* / epidemiology
  • California / epidemiology
  • Cross-Sectional Studies
  • Fatigue Syndrome, Chronic* / epidemiology
  • Fatigue Syndrome, Chronic* / virology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Prevalence
  • SARS-CoV-2* / isolation & purification
  • Surveys and Questionnaires
  • Young Adult

Grants and funding

This work was supported by the Centers for Disease Control and Prevention via a cooperative agreement with the California Emerging Infections Program [6NU50CK000452-04-05] for Project Surveillance to Optimize Protocols for Early Identification and Subgrouping of ME/CFS (STOP ME/CFS) and the COVID Standardized Evaluation of Long-term Effects (COVID-SELECT) and a sub-contract with Kaiser Permanente Northern California (JS), National Cancer Institute of the National Institutes of Health under Award Number U01CA260584 as part of the Serological Sciences Network (SeroNet) (JS) and the Physician Researcher Program of The Permanente Medical Group Delivery Science and Applied Research Program (JS).