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AQP4-IgG autoimmunity in Japan and Germany: differences in clinical profiles and prognosis in seropositive neuromyelitis optica spectrum disorders

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Item Type:Article
Title:AQP4-IgG autoimmunity in Japan and Germany: differences in clinical profiles and prognosis in seropositive neuromyelitis optica spectrum disorders
Creators Name:Asseyer, S., Masuda, H., Mori, M., Bellmann-Strobl, J., Ruprecht, K., Siebert, N., Cooper, G., Chien, C., Duchow, A., Schließeit, J., Liu, J., Sugimoto, K., Uzawa, A., Ohtani, R., Paul, F., Brandt, A.U., Kuwabara, S. and Zimmermann, H.G.
Abstract:BACKGROUND: Clinical outcomes in neuromyelitis optica spectrum disorders (NMOSD) vary across different regions. OBJECTIVE: To describe clinical profiles in Japanese and German NMOSD patients. METHODS: Medical records of aquaporin-4-immunoglobulin G (AQP4-IgG) positive NMOSD patients from Japan (n = 54) and Germany (n = 38) were retrospectively analyzed. RESULTS: The disability status was similar between both cohorts, although Japanese patients had a longer disease duration (13.3 ± 11.1 vs. 8.1 ± 6.9 years, p = 0.018) but similar relapse rates. Optic neuritis and myelitis were the most frequent attacks in both cohorts. Brain attacks occurred more frequently in Japanese patients (40.7% vs. 15.8%, p = 0.020). The time from disease onset (median [interquartile range] 2.3 [0.3-10.1] vs. 0.6 [0.2-1.9] years, p = 0.009) and the number of attacks (2.5 [1-7] vs. 2 [1-3], p = 0.047) until start of the first immunotherapy were higher in the Japanese cohort. Rituximab was the most common drug in the German cohort (52.6%) and not given in the Japanese cohort (p < 0.001), where oral prednisolone was the most common drug (92.6% vs. 15.8%, p < 0.001). The frequency of autoimmune comorbidities was higher in the German cohort (39.5% vs. 18.5%, p = 0.047). CONCLUSION: Compared with Japanese NMOSD patients, German patients presented with similar disability despite shorter disease duration and earlier and more frequent immunosuppressive therapy.
Keywords:Anti-Aquaporin 4 Antibodies, Autoimmune Diseases, Ethnicity, Immunotherapy, Neuromyelitisoptica Spectrum Disorders
Source:Multiple Sclerosis Journal Experimental Translational and Clinical
ISSN:2055-2173
Publisher:Sage Publications
Volume:7
Number:2
Page Range:205521732110068
Date:1 April 2021
Official Publication:https://doi.org/10.1177/20552173211006862
PubMed:View item in PubMed

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