Plasma Neurofilament Light Chain: A Potential Biomarker for Neurological Dysfunction in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
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Published:2024-07-11
Issue:7
Volume:12
Page:1539
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ISSN:2227-9059
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Container-title:Biomedicines
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language:en
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Short-container-title:Biomedicines
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
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