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. 2018 Feb 13;141(4):1063–1074. doi: 10.1093/brain/awy010

Table 1.

Clinical characteristics of patients with NMOSD

Patient number Age at sampling Sex Ethnicity Disease localization Time since first event (days) Time since last relapse (days) Duration of IT (days) Current IT (daily dose) Serum AQP4-IgG level (ΔMFI)
1 41 F Caucasian TM 1741 664 1199 Pred 15 mg 26 610
2 67 F Caucasian TM 1224 1141 1218 AZA 125 mg 15 267
3 36 F Asian ON and TM 7653 72 1442 Pred 20 mg; MMF 3 g 6126
4 50 F African TM 433 433 413 Pred 25 mg; MMF 1.5 g 3080
5 44 M Caucasian TM 2364 93 2344 Pred 10 mg; MMF 2.5 g 1863
6 55 F Caucasian ON 1728 1671 1708 MMF 2.5 g 1742
7 67 F Caucasian TM 3411 1798 1788 Pred 10 mg; MMF 2 g 1350
8 75 F Caucasian TM 688 688 668 Pred 10 mg; MMF 2 g 422
9 52 F Caribbean ON and TM 1125 667 1120 Pred 15 mg; MMF 2 g 209
10 18 F African Brain, TM 12 12 12 Pred 40 mg 91
11 57 F Caucasian TM 8589 2958 3108 RTX 402
12 37 F Caribbean Brain, ON and TM 3609 47 3243 Pred 20 mg; RTX 235

Serum AQP4-IgG levels determined by flow cytometry as described in Fig. 3 (ΔMFI, as defined in Methods). AZA = azathioprine; IT = immunotherapy; MMF = mycophenolate mofetil; ON = optic neuritis; Pred = prednisolone; TM = transverse myelitis; RTX = rituximab. Only Patients 11 and 12 ever received rituximab. Lymphocyte subsets are presented in Supplementary Table 1.