Abstract
Background: Neurofilament light chain (NF-L) levels reflect axonal damage in different conditions, including demyelinating disorders. Objectives: We aimed to compare serum NF-L levels in patients with aquaporin-4 antibodies (AQP4- Ab), myelin oligodendrocyte antibodies (MOG-Ab) and seronegative cases with neuromyelitis optica spectrum disorders and related disorders. Methods: We analysed AQP4-Ab and MOG-Ab with cell-based assay and NF-L with ultrasensitive electrochemiluminescence immunoassay. Results: Median NF-L levels were increased in 25 AQP4-Ab-positive patients (59 pg/ml) as compared with 22 MOG-Ab-positive cases (25 pg/ml), 52 seronegative patients (18 pg/ml), 25 multiple sclerosis patients (12 pg/ml) and 14 healthy controls (12 pg/ml). Conclusions: Increased serum levels of NF-L in patients with AQP4-Ab or MOG-Ab might reflect an ongoing axonal damage and a more malignant disease course.
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Mariotto, S., Farinazzo, A., Monaco, S., Gajofatto, A., Zanusso, G., Schanda, K., … Ferrari, S. (2017). Serum neurofilament light chain in NMOSD and related disorders: Comparison according to aquaporin-4 and Myelin Oligodendrocyte glycoprotein antibodies status. Multiple Sclerosis Journal - Experimental, Translational and Clinical, 3(4). https://doi.org/10.1177/2055217317743098
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