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. 2022 Apr 12;62:103800. doi: 10.1016/j.msard.2022.103800

Table 1.

Clinical and demographic characteristics of the study cohort.

MS patients (N = 96) Healthy Controls (N = 21)
Gender, n (%)
▒Female 57 (59.4) 11 (52.4)
▒Male 39 (40.6) 10 (47.6)
Age, years
▒Mean age (±SD) 40.7 (±10.5) 48.3 (±10.8)
▒IQR (25–75) 14.5 20.5
EDSS, mean (range) 1.9 (0–6.5)
DMTs duration, mean (months ± SD) 50.2 (±41.5)
MS type, n (%)
▒RRMS 91 (94.8)
▒PPMS 1 (1.04)
▒SPMS 4 (4.2)
DMTs, n (%)
▒Interferon -β 1a 19 (19.8)
▒Natalizumab 14 (14.6)
▒Dimethyl fumarate 14 (14.6)
▒Ocrelizumab 13 (13.5)
▒Fingolimod 13 (13.5)
▒Teriflunomide 8 (8.3)
▒Cladribine 8 (8.3)
▒Glatiramer acetate 7 (7.4)

DMTs: Disease modifying therapy; EDSS: Expanded disability status scale; IQR: Interquartile range; MS: Multiple sclerosis; PPMS: Primary progressive multiple sclerosis; RRMS: Relapsing remitting multiple sclerosis; SPMS: Secondary progressive multiple sclerosis.