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. 2019 Jul 25;16:154. doi: 10.1186/s12974-019-1521-5

Table 1.

Clinical characteristics of patients. Age (W = 370, p = 0.542) and sex (χ2 = 0.937, p = 0.333) did not differ between MOG-IgG-seropositive patients and HCs

HC MOG-IgG-seropositive patients
Subjects [N] 28 24
Number of eyes [N] 56 38
F/U [median years (min, max)] 1.9 (0.8–3.3) 1.9 (0.6–2.8)
Age [mean (SD)]; [range at baseline] 43.12 (9.76); [11–68] 40.66 (13.53); [15–68]
Sex [male (%)] 6 (21.4) 9 (37.5)
Clinical phenotypes (MOG-IgG-associated diseases) ON (N = 7), NMOSD (N = 12), MS (N = 3), meningoencephalomyelitis (N = 2)
EDSS at baseline [median (IQR)] 2.5 (2.0; 3.0)
Disease duration at baseline in years [median (IQR)] 3.0(1.1; 8.8)
Eyes with a history of ON [EyeON+, N (%)] 20 (52.6%)
Patients with a history of ON [N (%)] 15 (62.5%)
Number of ON in EyeON+ [median (range)] 2 (1–8)
Eyes without a history of ON [EyeON-, N (%)] 18 (47.4%)
Time since ON [years; median (range)] 2.2 (0.4–14.9)
Eyes with contralateral ON during F/U [N (%)] 5 (13.2)
Treatment at baseline [N] AZA [4], MTX [1], NAT [1], RIX [8], IVIG [1], PRED [2], NONE [7]

Abbreviations: HC healthy controls, N number, SD standard deviation, F/U follow-up, AZA azathioprine, MTX methotrexate, NAT natalizumab, RIX rituximab, IVIG intravenous immunoglobulins, PRED prednisone, TOC tocilizumab, MMF mycophenolate mofetil, NONE no treatment