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Detection of Cerebrospinal Fluid Neurofilament Light Chain as a Marker for Alpha-Synucleinopathies

Authors :
Canaslan, Sezgi
Schmitz, Matthias
Villar Piqué, Anna
Maass, Fabian
Gmitterová, Karin
Varges, Daniela
Lingor, Paul
Llorens Torres, Franc
Hermann, Peter
Zerr, Inga
Source :
Frontiers in aging neuroscience 13, 717930 (2021). doi:10.3389/fnagi.2021.717930, Frontiers in Aging Neuroscience, Dipòsit Digital de la UB, Universidad de Barcelona
Publication Year :
2021
Publisher :
Frontiers Research Foundation, 2021.

Abstract

Alpha-synucleinopathies, such as Parkinson's disease (PD), dementia with Lewy bodies (DLB), and multiple system atrophy (MSA), are a class of neurodegenerative diseases. A diagnosis may be challenging because clinical symptoms partially overlap, and there is currently no reliable diagnostic test available. Therefore, we aimed to identify a suitable marker protein in cerebrospinal fluid (CSF) to distinguish either between different types of alpha-synucleinopathies or between alpha-synucleinopathies and controls. In this study, the regulation of different marker protein candidates, such as alpha-synuclein (a-Syn), neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), and total tau (tau) in different types of alpha-synucleinopathies, had been analyzed by using an ultrasensitive test system called single-molecule array (SIMOA). Interestingly, we observed that CSF-NfL was significantly elevated in patients with DLB and MSA compared to patients with PD or control donors. To differentiate between groups, receiver operating characteristic (ROC) curve analysis resulted in a very good diagnostic accuracy as indicated by the area under the curve (AUC) values of 0.87-0.92 for CSF-NfL. Furthermore, we observed that GFAP and tau were slightly increased either in DLB or MSA, while a-Syn levels remained unregulated. Our study suggests NfL as a promising marker to discriminate between different types of alpha-synucleinopathies or between DLB/MSA and controls.

Details

Language :
English
Database :
OpenAIRE
Journal :
Frontiers in aging neuroscience 13, 717930 (2021). doi:10.3389/fnagi.2021.717930, Frontiers in Aging Neuroscience, Dipòsit Digital de la UB, Universidad de Barcelona
Accession number :
edsair.pmid.dedup....30111aa5dd4c939e628b6485754e3251
Full Text :
https://doi.org/10.3389/fnagi.2021.717930