Table 1.
Healthy controls | MS patients | NMOSD patients | |
---|---|---|---|
Number of individuals | 31 | 86 | 41 |
Age (median, IQR) | 31 (27–34) | 45 (34–52) | 57 (45–64) |
Sex (n female) | 15 (48.4%) | 53 (61.6%) | 37 (90.2%) |
Subtype (n) | – |
RRMS: 63 (73.3%) SPMS: 15 (17.4%) PPMS: 5 (5.9%) |
AQP4+: 23 (56.1%) MOG+: 7 (17.1%) Seronegative: 3 (7.3%) Unknown: 8 (19.5%) |
Additional immune-mediated diseases (n) | Autoimmune thyroiditis (2), asthma bronchiale (1) | Autoimmune thyroiditis (10), asthma bronchiale (2), psoriasis (1), idiopathic myocarditis (1), celiac disease (1) | Autoimmune thyroiditis (3), myasthenia gravis (1), Sjögren syndrome (1), MCTD (1) |
Immunosuppressive medication (n) | – |
None: 24 (27.9%) Dimethyl fumarate: 15 (17.4%), glatiramer acetate: 14 (16.3%), interferon beta: 13 (15.1%), fingolimod: 7 (8.1%), teriflunomide: 5 (5.8%), methylprednisolone: 2 (2.3%), daclizumab: 2 (2.3%), rituximab: 1 (1.2%), ocrelizumab: 1 (1.2%), natalizumab 1 (1.2%) |
Rituximab: 19 (46.3%) Azathioprine: 9 (22.0%) None: 6 (14.6%) Prednisolone: 3 (7.3%) Mycophenolate: 2 (4.9%) Glatiramer acetate: 1 (2.4%) Unknown: 1 (2.4%) |
IQR interquartile range, RRMS relapse-remitting multiple sclerosis, SPMS secondary progressive multiple sclerosis, PPMS primary progressive multiple sclerosis, AQP4+ aquaporin-4 antibody positive, MOG+ myelin oligodendrocyte glycoprotein antibody positive, MCTD mixed connective tissue disease).