4.6 Article

Herpesviruses Serology Distinguishes Different Subgroups of Patients From the United Kingdom Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Biobank

Journal

FRONTIERS IN MEDICINE
Volume 8, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmed.2021.686736

Keywords

disease trigger; cutoff value; stratification; Epstein-Barr virus; human cytomegalovirus; varicella-zoster virus; human herpesvirus-6; herpes simplex virus 1 and 2

Funding

  1. Fundacao para a Ciencia e a Tecnologia, Portugal [UIDB/00006/2020, UIDB/04561/2020]
  2. ME Research UK (SCIO Charity) [SC036942]
  3. EUROMENE Cost Action [CA15111]
  4. Spanish State Research Agency (AEI) - European Regional Development Fund (ERDF) [MTM201676969-P]
  5. Competitive Reference Groups 2017-2020 from the Xunta de Galicia through the ERDF [ED431C 2017/38]
  6. National Institutes of Health (NIH) [2R01AI103629]
  7. Fred and Joan Davies Bequest
  8. ME Association
  9. ME Research UK
  10. Action for ME

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The study investigated the association between ME/CFS and chronic herpesvirus infections, analyzing serological data from different subgroups of patients. While the data suggested a potential differentiation of patient subgroups based on herpesvirus serology, this finding may be limited by the issue of multiple testing.
The evidence of an association between Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and chronic herpesviruses infections remains inconclusive. Two reasons for the lack of consistent evidence are the large heterogeneity of the patients' population with different disease triggers and the use of arbitrary cutoffs for defining seropositivity. In this work we re-analyzed previously published serological data related to 7 herpesvirus antigens. Patients with ME/CFS were subdivided into four subgroups related to the disease triggers: S-0-42 patients who did not know their disease trigger; S-1-43 patients who reported a non-infection trigger; S-2-93 patients who reported an infection trigger, but that infection was not confirmed by a lab test; and S-3-48 patients who reported an infection trigger and that infection was confirmed by a lab test. In accordance with a sensitivity analysis, the data were compared to those from 99 healthy controls allowing the seropositivity cutoffs to vary within a wide range of possible values. We found a negative association between S-1 and seropositivity to Epstein-Barr virus (VCA and EBNA1 antigens) and Varicella-Zoster virus using specific seropositivity cutoff. However, this association was not significant when controlling for multiple testing. We also found that S-3 had a lower seroprevalence to the human cytomegalovirus when compared to healthy controls for all cutoffs used for seropositivity and after adjusting for multiple testing using the Benjamini-Hochberg procedure. However, this association did not reach statistical significance when using Benjamini-Yekutieli procedure. In summary, herpesviruses serology could distinguish subgroups of ME/CFS patients according to their disease trigger, but this finding could be eventually affected by the problem of multiple testing.

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