Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14365/6362
Title: Comparative Efficacy of Rituximab Versus Azathioprine in the Treatment of MOG Antibody-Associated Disease (MOGAD)
Authors: Sen, Sedat
Kurtuncu, Murat
Demir, Serkan
Gunduz, Tuncay
Demirel, Ezgi
Tutuncu, Melih
Tuncer, Asli
Keywords: Myelin Oligodendrocyte Glycoprotein
Associated Disease
MOGAD
Azathioprine
Rituximab
Disability
Publisher: Elsevier
Abstract: Background: Azathioprine (AZA) and rituximab (RTX) are frequently used drugs in the treatment of Myelin Oligodendrocyte Glycoprotein Associated Disease (MOGAD). Objectives: The aim of this study was to evaluate the efficacy and safety data of AZA and RTX treatments in MOGAD. Methods: Patients diagnosed according to the 2023 MOGAD diagnostic criteria and receiving AZA or RTX treatment were included in the study. Results: In 142 patients included in the study, the female/male value was 1.2. The rate of OCB positivity in MOGAD patients was 22.6 %. Patients on RTX had higher EDSS values than patients on AZA. However, the RTX group demonstrated a more pronounced improvement in disability, reflected by a greater negative trend in the Delta EDSS values. The attack-free rate was 78 % in the RTX group and 68 % in the AZA group during their treatment period. Both groups had no difference in the time of the first attack. The main factor affecting the time to first attack was having a higher EDSS at the time of treatment initiation. The survival analysis found that EDSS scores improved significantly in patients treated with RTX. Conclusion: Although survival analyses for both treatments appear to be similar, using RTX provides better EDSS scores.
URI: https://doi.org/10.1016/j.jneuroim.2025.578686
https://hdl.handle.net/20.500.14365/6362
ISSN: 0165-5728
1872-8421
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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