Comparative efficacy of rituximab versus azathioprine in the treatment of MOG antibody-associated disease (MOGAD)

dc.authorid0000-0001-8048-6845
dc.authorid0000-0003-3286-2652
dc.authorid0000-0003-4395-5141
dc.authorid0000-0003-4241-0908
dc.authorid0000-0002-9851-7002
dc.authorid0000-0002-9035-8537
dc.authorid0000-0003-4148-2539
dc.contributor.authorUzunköprü, Cihat
dc.contributor.authorTütüncü, Melih
dc.contributor.authorDemirel Özbek, Ezgi
dc.contributor.authorGündüz, Tuncay
dc.contributor.authorDemir, Serkan
dc.contributor.authorKürtüncü, Murat
dc.contributor.authorŞen, Sedat
dc.contributor.authorTepe, Nermin
dc.date.accessioned2026-03-31T11:33:22Z
dc.date.issued2025
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
dc.descriptionTepe, Nermin (Balikesir Author)
dc.description.abstractBackground: 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 ΔEDSS 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
dc.identifier.doi10.1016/j.jneuroim.2025.578686
dc.identifier.endpage7
dc.identifier.issn0165-5728
dc.identifier.issn1872-8421
dc.identifier.pmid40694990
dc.identifier.scopus2-s2.0-105010881618
dc.identifier.scopusqualityQ1
dc.identifier.startpage1
dc.identifier.urihttps://doi.org/10.1016/j.jneuroim.2025.578686
dc.identifier.urihttps://hdl.handle.net/20.500.12462/23619
dc.identifier.volume407
dc.identifier.wos001539571200001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElseiver
dc.relation.ispartofJournal of Neuroimmunology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectMyelin Oligodendrocyte Glycoprotein
dc.subjectAssociated Disease
dc.subjectMogad
dc.subjectAzathioprine
dc.subjectRituximab
dc.subjectDisability
dc.titleComparative efficacy of rituximab versus azathioprine in the treatment of MOG antibody-associated disease (MOGAD)
dc.typeArticle

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