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. 2023 Dec 11;81(2):143–153. doi: 10.1001/jamaneurol.2023.4737

Table. Demographic and Clinical Characteristics.

MS (n = 550) CIS (n = 49) AQP4-positive NMOSD (n = 19) Seronegative-NMOSD (n = 22) MOGAD (n = 17) Migraine (n = 96) Inflammatory vasculopathies (n = 29) Cerebrovascular disease (n = 63) Fabry disease (n = 57) Healthy control individuals (n = 149)
Male, No. (%) 198 (36) 15 (31) 3 (16) 3 (14) 11 (65) 20 (21) 10 (34) 29 (46) 26 (46) 48 (32)
Female, No. (%) 352 (64) 34 (69) 16 (84) 19 (86) 6 (35) 76 (79) 19 (66) 34 (54) 31 (54) 101 (68)
Age, mean (SD), y 41.9 (12.5) 37.2 (9.8) 47.3 (14.1) 47.3 (13.9) 39.8 (11.7) 42.3 (11.9) 51.9 (15.7) 63.2 (13.3) 42.3 (12.5) 51.4 (12.4)
Disease duration, median (IQR), y 6.0 (1.5-13.5) 0.4 (0.3-0.9) 3.6 (1.9-5.0) 7.0 (2.0-11.0) 4.3 (0.6-7.8) NA NA NA NA NA
EDSS score, median (IQR) 2.0 (1.5-3.5) 2.0 (1.0-2.5) 3.25 (2.0-6.0) 3.0 (2.0-5.0) 1.5 (1.0-2.0) NA NA NA NA NA
Disease subgroups, No. (%) RRMS: 462 (84); SPMS: 62 (11); PPMS: 26 (5) NA NA NA NA NA Sjögren syndrome: 19 (66); SLE: 4 (14); Behçet disease: 3 (10); AAV: 2 (7); Susac syndrome: 1 (3) CSVD: 53 (84); PFO: 10 (16) NA NA

Abbreviations: AAV, anti-neutrophil cytoplasmic antibody-associated vasculitis; AQP4, aquaporin-4 antibody; CIS, clinically isolated syndrome; CSVD, cerebral small vessel disease; MOGAD, myelin oligodendrocyte glycoprotein antibody-associated disease; MS, multiple sclerosis; NA, not applicable; NMOSD, neuromyelitis optica spectrum disorder; PFO, patent foramen ovale; PPMS, primary progressive multiple sclerosis; RRMS, relapsing-remitting multiple sclerosis; SLE, systemic lupus erythematosus; SPMS, secondary progressive multiple sclerosis.