Worse recovery from acute attacks and faster disability accumulation highlights the unmet need for improved treatment in patients with late-onset neuromyelitis optica spectrum disorders (COPTER-LO study).
作者信息
Kretschmer Julian Reza, Tkachenko Daria, Kümpfel Tania, Havla Joachim, Engels Daniel, Paul Friedemann, Schindler Patrick, Bellmann-Strobl Judith, Berthele Achim, Giglhuber Katrin, Zappe Clarissa, Klotz Luisa, Revie Lisa, Dawin Eva, Senel Makbule, Tumani Hayrettin, Bergh Florian Then, Warnke Clemens, Kraemer Markus, Walter Annette, Bayas Antonios, Zettl Uwe K, Lauenstein Ann-Sophie, Yalachkov Yavor, Etgen Thorleif, Kaste Matthias, Luessi Felix, Gingele Stefan, Passoke Sarah, Weber Martin S, Sieb Jörn Peter, Haarmann Axel, Oschmann Patrick, Rothhammer Veit, Geis Christian, Kowarik Markus C, Kern Peter, Grothe Matthias, Stephanik Heike, Angstwurm Klemens, Hoffmann Frank, Wallwitz Ulrike, Wildemann Brigitte, Jarius Sven, Stellmann Jan-Patrick, Pakeerathan Thivya, Schwake Carolin, Ayzenberg Ilya, Kleiter Ingo, Fischer Katinka, Aktas Orhan, Ringelstein Marius, Häußler Vivien, Trebst Corinna, Hümmert Martin W
机构信息
Department of Neurology, Hannover Medical School, Hannover, Germany.
Institute of Clinical Neuroimmunology, LMU University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
出版信息
Front Immunol. 2025 Apr 11;16:1575613. doi: 10.3389/fimmu.2025.1575613. eCollection 2025.
OBJECTIVE
This study analyzed clinical characteristics, attack recovery and long-term disability accumulation in late-onset (LO ≥ 50 years at onset) versus early-onset (EO < 50 years) NMOSD.
METHODS
This multicenter cohort study included demographic and clinical data from 446 NMOSD patients collected from 35 German Neuromyelitis Optica Study Group (NEMOS) centers. Time to disability milestones was estimated through Kaplan-Meier analysis and Cox proportional hazard regression models adjusted for sex, year of onset, immunotherapy exposure and antibody status. Generalized estimating equations (GEE) were used to compare attack outcomes.
RESULTS
Of the 446 NMOSD patients analyzed (83.4% female, 85.4% AQP4-IgG-positive, median age at disease onset = 43 years), 153 had a late-onset (34.3%). AQP4-IgG+ prevalence was higher in LO- than in EO-NMOSD (94.1% vs. 80.9%, <0.001). Optic neuritis at onset was more frequent in EO-NMOSD (27.4% vs. 42.6%, <0.002), whereas myelitis was more common in LO-NMOSD (58.4% vs. 37.9%, <0.001). Both groups had similar annualized attack rates (AAR, 0.51 vs. 0.54, =0.352), but attack recovery was poorer (complete remission in 15.6% vs. 27.4%, <0.001) and relapse-associated worsening (RAW) was higher in LO-NMOSD (RAW: 3 vs. 0.5, <0.001). Long-term immunotherapy use was comparable. LO-NMOSD exhibited faster progression to disability endpoints (EDSS 4: HR = 2.64, 95% CI=1.81-3.84).
INTERPRETATION
LO-NMOSD patients presented more often with myelitis, experienced worse attack outcomes and faster disability accumulation, despite comparable AAR, acute attack treatment and long-term treatment regimens. Accordingly, therapeutic strategies for attack and prophylactic treatment in LO-NMOSD have to be improved.
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