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| Item Type: | Article |
|---|---|
| Title: | Time to disability milestones and annualized relapse rates in NMOSD and MOGAD |
| Creators Name: | Duchow, A. and Bellmann-Strobl, J. and Friede, T. and Aktas, O. and Angstwurm, K. and Ayzenberg, I. and Berthele, A. and Dawin, E. and Engels, D. and Fischer, K. and Flaskamp, M. and Giglhuber, K. and Grothe, M. and Havla, J. and Hümmert, M.W. and Jarius, S. and Kaste, M. and Kern, P. and Kleiter, I. and Klotz, L. and Korporal-Kuhnke, M. and Kraemer, M. and Krumbholz, M. and Kümpfel, T. and Lohmann, L. and Ringelstein, M. and Rommer, P. and Schindler, P. and Schubert, C. and Schwake, C. and Senel, M. and Bergh, F.T. and Tkachenko, D. and Tumami, H. and Trebst, C. and Vardakas, I. and Walter, A. and Warnke, C. and Weber, M.S. and Wickel, J. and Wildemann, B. and Winkelmann, A. and Paul, F. and Stellmann, J.P. and Häußler, V. |
| Abstract: | OBJECTIVE: To investigate accumulation of disability in neuromyelitis optica spectrum disorder (NMOSD) and myelin oligodendrocyte glycoprotein-antibody-associated disease (MOGAD) in a changing treatment landscape. We aimed to identify risk factors for the development of disability milestones in relation to disease duration, number of attacks, and age. METHODS: We analyzed data from individuals with NMOSD and MOGAD from the German Neuromyelitis Optica Study Group registry. Applying survival analyses, we estimated risk factors and computed time to disability milestones as defined by the EDSS. RESULTS: We included 483 patients: 298 AQP4-IgG(+) NMOSD, 52 AQP4-IgG(-)/MOG-IgG(-) NMOSD patients, and 133 patients with MOGAD. Despite comparable annualized attack rates, disability milestones occurred earlier and after less attacks in NMOSD patients than MOGAD patients (median time to EDSS 3: AQP4-IgG+ NMOSD 7.7 (95%CI 6.6 - 9.6) years, AQP4-IgG(-)/MOG-IgG(-) NMOSD 8.7) years, MOGAD 14.1 (95%CI 10.4 - 27.6) years; EDSS 4: 11.9 (95%CI 9.7 - 14.7), 11.6 (95% lower CI 7.6) and 20.4 (95% lower CI 14.1) years; EDSS 6: 20.1 (95%CI 16.5 - 32.1), 20.7 (95% lower CI 11.6), and 37.3 (95% lower CI 29.4) years; and EDSS 7: 34.2 (95% lower CI 31.1) for AQP4-IgG(+) NMOSD). Higher age at onset increased the risk for all disability milestones, while risk of disability decreased over time. INTERPETATION: AQP4-IgG(+) NMOSD, AQP4-IgG(-)/MOG-IgG(-) NMOSD and MOGAD patients show distinctive relapse-associated disability progression, with MOGAD having a less severe disease course. Investigator-initiated research has led to increasing awareness and improved treatment strategies appearing to ameliorate disease outcomes for NMOSD and MOGAD. |
| Keywords: | Aquaporin 4, Autoantibodies, Immunoglobulin G, Myelin-Oligodendrocyte Glycoprotein, Neuromyelitis Optica, Recurrence |
| Source: | Annals of Neurology |
| ISSN: | 0364-5134 |
| Publisher: | Wiley |
| Volume: | 95 |
| Number: | 4 |
| Page Range: | 720-732 |
| Date: | April 2024 |
| Official Publication: | https://doi.org/10.1002/ana.26858 |
| PubMed: | View item in PubMed |
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