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

Authors :
Azcue, Naiara
Tijero-Merino, Beatriz
Acera, Marian
Pérez-Garay, Raquel
Fernández-Valle, Tamara
Ayo-Mentxakatorre, Naia
Ruiz-López, Marta
Lafuente, Jose Vicente
Gómez Esteban, Juan Carlos
Del Pino, Rocio
Source :
Biomedicines; Jul2024, Vol. 13 Issue 7, p1539, 13p
Publication Year :
2024

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22279059
Volume :
13
Issue :
7
Database :
Complementary Index
Journal :
Biomedicines
Publication Type :
Academic Journal
Accession number :
178697539
Full Text :
https://doi.org/10.3390/biomedicines12071539