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Circulating FGF-21 as a Disease-Modifying Factor Associated with Distinct Symptoms and Cognitive Profiles in Myalgic
Ghazaleh Azimi1,2,3,4, Wesam Elremaly1,3,4, Mohamed Elbakry1,3,4,5
1Viscogliosi Laboratory in Molecular Genetics of Musculoskeletal Diseases, Office 2.17.027, Azrieli Research Center, CHU Sainte-Justine, 3175 Cote-Ste-Catherine Road, Montreal, QC H3T 1C5, Canada.
Fibroblast growth factor 21 (FGF-21) may help identify subtypes in Myalgic Encephalomyelitis (ME) and Fibromyalgia (FM). Stratifying patients by FGF-21 levels revealed distinct symptom and cognitive profiles, suggesting its potential as a biomarker for personalized treatment.
Area of Science:
- Biochemistry
- Immunology
- Neurology
Background:
- Myalgic encephalomyelitis (ME) and fibromyalgia (FM) are complex syndromes lacking objective diagnostic biomarkers.
- Fibroblast growth factor 21 (FGF-21), a metabolic hormone, is being investigated for its potential role in these conditions.
Purpose of the Study:
- To investigate plasma FGF-21 levels as a potential biomarker for distinguishing subtypes within ME and FM patient populations.
- To explore the correlation between FGF-21 levels and symptom burden, cognitive function, and post-exertional malaise (PEM).
Main Methods:
- Cross-sectional study measuring plasma FGF-21 in 250 ME/FM patients and 54 healthy controls.
- Categorization of participants into low, normal, and high FGF-21 groups.
- Assessment of symptoms and cognition using validated questionnaires and a cognitive testing platform, with a mechanical maneuver to induce PEM.
Main Results:
- Elevated FGF-21 levels were common in ME and ME + FM groups but showed wide variation.
- Stratification by FGF-21 levels, not diagnosis alone, revealed distinct clinical profiles.
- Specific FGF-21 levels correlated with varied symptom severity, cognitive performance, and PEM perception across ME and FM subtypes.
Conclusions:
- FGF-21 shows promise as a biomarker for identifying clinically relevant ME and FM subtypes.
- Findings support the development of personalized treatment strategies (precision medicine) for ME and FM.
- Highlights the need for objective tools to assess post-exertional malaise (PEM).

