Ayrignac, XavierLe Bars, EmmanuelleDuflos, ClaireHirtz, ChristopheMaceski, Aleksandra MaleskaCarra-Dalliere, ClarisseCharif, MahmoudPinna, FredericPrin, Paulinede Champfleur, Nicolas MenjotDeverdun, JeremyKober, TobiasMarechal, BenedicteFartaria, Mario JoaoJerez, Ricardo CorredorLabauge, PierreLehmann, Sylvain2020-08-052020-08-052020-08-052020-07-0210.1038/s41598-020-67934-2https://infoscience.epfl.ch/handle/20.500.14299/170622WOS:000550002500031Neurofilament 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<plus/minus>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.Multidisciplinary SciencesScience & Technology - Other Topicscerebrospinal-fluidneuronal markersneurofilamentbiomarkerdamagetext::journal::journal article::research article