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. 2019 Nov 29;10:2725. doi: 10.3389/fimmu.2019.02725

Table 1.

Epidemiological information of the study population.

NMOSD (n = 20) MS (n = 17) HD (n = 23) SLE (n = 15)
Age (median and interquartile range) 48 (34.0–56.5) 47 (36.0–51.0) 29 (27.0–43.5) 40 (31.0–48.0)
Sex (n and percentage female) 17 (85.0) 5 (29.4) 15 (65.2) 14 (93.3)
Time since disease onset (in years, median and interquartile range) 7.0 (3.0–8.8) 9.7 (4.6–15.4) 13.0 (5.5–17.7)
Time since last relapse (in years, median and interquartile range) n.d. 3.4 (1.5–8.3) n.d.
Clinical severity (EDSS for MS and NMOSD, SLEDAI for SLE median and interquartile range) 3 (1.5–4.5) 4 (2.0–5.0) 5 (2.0 – 7.0)
Treatments (n, percentage) Rituximab n = 8 (40.0), Azathioprine and untreated each n = 4 (20.0), Mycophenolate n = 3 (15.0), Teriflunomide n = 1 (5.0) Dimethylfumarat n = 6 (35.3), Interferon beta n = 4 (23.4), untreated n = 3 (17.6), Daclizumab, intrathecal Steroids, Glatirameracetate and Fingolimod each n = 1 (5.9) Prednisolone n = 15 (100.0), Hydroxychloroquine n = 7 (46.7), Mycophenolate n = 3 (20.0), Azathioprine, Methotrexate and Cyclosporine A each n = 2 (13.3), Rituximab n = 1 (6.67)
Autoantibody Status (n, percentage) AQP-4 n = 8 (40.0)
MOG n = 4 (20.0)
% of LDGs (median and interquartile range) 2.1 (1.1–4.1) 0.9 (0.57–1.63) 0.2 (0.2–0.4) 4.3 (1.0–9.5)
% of CD16high LDGs (median and interquartile range) 91.2 (77.2–94.9) 87.8 (67.3–94.4) 65.6 (53.7–79.9) 84.6 (64.6–89.6)

n.d. no data.