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. 2022 Dec 24;270(4):2048–2058. doi: 10.1007/s00415-022-11529-6

Table 1.

Patient demographics and clinical characteristics

Clinical/Epidemiological Factor Patients, n (%) (Total N = 542)
Median length of follow-up (years) 2.22 (0.22–6.26)
Female sex 469 (86.5)
Race/ethnicity
 Asian 47 (8.7)
 Black or African American 124 (22.9)
 Hispanic or Latino 60 (11.1)
 White 311 (57.4)
Anti–AQP4-IgG +  455 (83.9)
Age at disease onset
 < 30 years 151 (27.9)
 30–49 years 260 (48)
 ≥ 50 years 131 (24.2)
Disease duration before study entrance
 < 1 year 98 (18.1)
 1–5 years 186 (34.3)
 > 5 years 258 (47.6)
Pre-study ARR (self-reported)
 Rate < 0.25 249 (45.9)
 Rate 0.25–0.75 166 (30.6)
 Rate > 0.75 127 (23.4)
Disease onset phenotype
 ON only and ON + BR 177 (32.7)
 TM only and TM + BR 193 (35.6)
 ON + TM and ON + TM + BR 58 (10.7)
 BR only 35 (6.4)
 Confirmed through symptoms 79 (14.6)
Comorbidities
 Any other autoimmune comorbidity 153 (28.2)
  Lupus 37 (6.8)
  Sjögren syndrome 34 (6.3)
  Rheumatoid arthritis 15 (2.8)
  Myasthenia gravis 11 (2.0)
Treatment at study starta
 Rituximab 230 (42.4)
 Mycophenolate mofetil 92 (17.0)
 Maintenance steroids 67 (12.4)
 Azathioprine 64 (11.8)
 Tocilizumab 4 (0.7)

Anti–AQP4-IgG, aquaporin 4 autoantibody; ARR, annualized relapse rate; BR, brain involvement; ON, optic neuritis; TM, transverse myelitis

aTreatment categories are not mutually exclusive. Each is a binary yes/no variable (“yes” level is summarized in this table). It is possible that patients were not on any treatment, multiple treatments, or other treatments on Day 1