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Serum GFAP in multiple sclerosis: correlation with disease type and MRI markers of disease severity

Neurofilament light chain (NfL) has been demonstrated to correlate with multiple sclerosis disease severity as well as treatment response. Nevertheless, additional serum biomarkers are still needed to better differentiate disease activity from disease progression. The aim of our study was to assess...

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Detalles Bibliográficos
Autores principales: Ayrignac, Xavier, Le Bars, Emmanuelle, Duflos, Claire, Hirtz, Christophe, Maleska Maceski, Aleksandra, Carra-Dallière, Clarisse, Charif, Mahmoud, Pinna, Frédéric, Prin, Pauline, Menjot de Champfleur, Nicolas, Deverdun, Jérémy, Kober, Tobias, Marechal, Bénédicte, Fartaria, Mario Joao, Corredor Jerez, Ricardo, Labauge, Pierre, Lehmann, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331703/
https://www.ncbi.nlm.nih.gov/pubmed/32616916
http://dx.doi.org/10.1038/s41598-020-67934-2
Descripción
Sumario:Neurofilament light chain (NfL) has been demonstrated to correlate with multiple sclerosis disease severity as well as treatment response. Nevertheless, additional serum biomarkers are still needed to better differentiate disease activity from disease progression. The aim of our study was to assess serum glial fibrillary acid protein (s-GFAP) and neurofilament light chain (s-NfL) in a cohort of 129 multiple sclerosis (MS) patients. Eighteen primary progressive multiple sclerosis (PPMS) and 111 relapsing remitting MS (RRMS) were included. We showed that these 2 biomarkers were significantly correlated with each other (R = 0.72, p < 0.001). Moreover, both biomarkers were higher in PPMS than in RRMS even if multivariate analysis only confirmed this difference for s-GFAP (130.3 ± 72.8 pg/ml vs 83.4 ± 41.1 pg/ml, p = 0.008). Finally, s-GFAP was correlated with white matter lesion load and inversely correlated with WM and GM volume. Our results seem to confirm the added value of s-GFAP in the context of multiple sclerosis.