Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia: PR3-versus MPO-ANCA-associated

Charmaine van Eeden1,2, Naima Mohazab1,2, Desiree Redmond1,2

  • 1Division of Rheumatology, Department of Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.

Abstract

Insights

Many patients with ANCA-vasculitis (AAV) experience fatigue meeting criteria for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Fatigue differs between PR3- and MPO-ANCA types, suggesting distinct mechanisms and potential for tailored treatments.

Area of Science:

  • Rheumatology
  • Immunology
  • Neurology

Background:

  • Persistent fatigue significantly impacts the quality of life for patients with ANCA-associated vasculitis (AAV).
  • Fatigue symptoms in AAV patients often resemble those seen in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia.
  • Existing research has not fully explored the differences in fatigue manifestations between PR3-ANCA and MPO-ANCA disease subtypes.

Purpose of the Study:

  • To compare fatigue and its associated factors in healthy controls, AAV patients, and fibromyalgia controls.
  • To investigate potential differences in fatigue between PR3-ANCA and MPO-ANCA patients.
  • To explore the relationship between fatigue and clinical factors in AAV.

Main Methods:

  • Utilized Canadian consensus criteria for ME/CFS diagnosis and American College of Rheumatology criteria for fibromyalgia diagnosis.
  • Assessed patient-reported outcomes including cognitive failure, depression, anxiety, and sleep disturbances.
  • Collected clinical data such as Birmingham Vasculitis Activity Score (BVAS), vasculitis damage index, C-reactive protein (CRP), and body mass index (BMI).

Main Results:

  • Over half of the 52 AAV patients met diagnostic criteria for ME/CFS, with a significant portion also having comorbid fibromyalgia.
  • MPO-ANCA patients reported higher rates of fatigue with symptoms more akin to fibromyalgia controls compared to PR3-ANCA patients.
  • Fatigue in PR3-ANCA patients was correlated with inflammatory markers, suggesting different underlying pathophysiologies.

Conclusions:

  • A substantial number of AAV patients experience fatigue severe enough to meet ME/CFS criteria.
  • The distinct fatigue associations between PR3-ANCA and MPO-ANCA patients indicate potentially different underlying mechanisms.
  • Future research should stratify by ANCA serotype to inform personalized treatment strategies for AAV patients with ME/CFS.