Plasma Neurofilament Light Chain: A Potential Biomarker for Neurological Dysfunction in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Author:

Azcue Naiara1ORCID,Tijero-Merino Beatriz123,Acera Marian1,Pérez-Garay Raquel4,Fernández-Valle Tamara12,Ayo-Mentxakatorre Naia1,Ruiz-López Marta12,Lafuente Jose Vicente5ORCID,Gómez Esteban Juan Carlos1235ORCID,Del Pino Rocio1ORCID

Affiliation:

1. Neurodegenerative Diseases Group, Biobizkaia Health Research Institute, 48903 Barakaldo, Spain

2. Department of Neurology, Cruces University Hospital-OSAKIDETZA, 48903 Barakaldo, Spain

3. CIBERNED-CIBER, Institute Carlos III, 28029 Madrid, Spain

4. Clinical Analysis Service, Cruces University Hospital, 48903 Barakaldo, Spain

5. Department of Neurosciences, University of the Basque Country UPV/EHU, 48940 Leioa, Spain

Abstract

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex disorder characterized by heterogeneous symptoms, which lack specific biomarkers for its diagnosis. This study aimed to investigate plasma neurofilament light chain (NfL) levels as a potential biomarker for ME/CFS and explore associations with cognitive, autonomic, and neuropathic symptoms. Here, 67 ME/CFS patients and 43 healthy controls (HCs) underwent comprehensive assessments, including neuropsychological evaluation, autonomic nervous system (ANS) testing, and plasma NfL level analysis. ME/CFS patients exhibited significantly higher plasma NfL levels compared to HC (F = 4.30, p < 0.05). Correlations were observed between NfL levels and cognitive impairment, particularly in visuospatial perception (r = −0.42; p ≤ 0.001), verbal memory (r = −0.35, p ≤ 0.005), and visual memory (r = −0.26; p < 0.05) in ME/CFS. Additionally, higher NfL levels were associated with worsened autonomic dysfunction in these patients, specifically in parasympathetic function (F = 9.48, p ≤ 0.003). In ME/CFS patients, NfL levels explained up to 17.2% of the results in cognitive tests. Unlike ME/CFS, in HC, NfL levels did not predict cognitive performance. Elevated plasma NfL levels in ME/CFS patients reflect neuroaxonal damage, contributing to cognitive dysfunction and autonomic impairment. These findings support the potential role of NfL as a biomarker for neurological dysfunction in ME/CFS. Further research is warranted to elucidate underlying mechanisms and clinical implications.

Funder

Instituto de Salud Carlos III

European Union

Basque Government

Publisher

MDPI AG

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