Table 1.
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