Publication:
Impact of age at onset on relapse and disability in AQP4-IgG neuromyelitis optica spectrum disorder

dc.contributor.coauthorSiriratnam, Pakeeran
dc.contributor.coauthorJokubaitis, Vilija G.
dc.contributor.coauthorVan, Der Walt Anneke
dc.contributor.coauthorSanfilippo, Paul G.
dc.contributor.coauthorZhu, Chao
dc.contributor.coauthorEtemadifar, Masoud
dc.contributor.coauthorAl-Asmi, Abdullah
dc.contributor.coauthorLaureys, Guy
dc.contributor.coauthorMeca-Lallana, Jose E.
dc.contributor.coauthorFoschi, Matteo
dc.contributor.coauthorAlroughani, Raed
dc.contributor.coauthorGomez-Figueroa, Enrique
dc.contributor.coauthorHabek, Mario
dc.contributor.coauthorKhoury, Samia J.
dc.contributor.coauthorSimo, Magdolna
dc.contributor.coauthorSinghal, Bhim Sen G.
dc.contributor.coauthorJakob, Gregor Brecl
dc.contributor.coauthorFabis-Pedrini, Marzena J.
dc.contributor.coauthorSoysal, Aysun
dc.contributor.coauthorKermode, Allan G.
dc.contributor.coauthorShaygannejad, Vahid
dc.contributor.coauthorKubala, Havrdova Eva
dc.contributor.coauthorMillan-Pascual, Jorge
dc.contributor.coauthorRoos, Izanne
dc.contributor.coauthorMccombe, Pamela Ann
dc.contributor.coauthorNytrova, Petra
dc.contributor.coauthorBoz, Cavit
dc.contributor.coauthorSurcinelli, Andrea
dc.contributor.coauthorKalincik, Tomas
dc.contributor.coauthorPatti, Francesco
dc.contributor.coauthorHuda, Saif
dc.contributor.coauthorButzkueven, Helmut
dc.contributor.coauthorMonif, Mastura
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorAltıntaş, Ayşe
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2026-07-02T07:30:26Z
dc.date.issued2026
dc.description.abstractBackground and Objectives Previous studies have reported inconsistent findings regarding the impact of age at onset on relapse risk in aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder (AQP4-IgG NMOSD), although older disease onset has been linked to more rapid disability accrual. This is in contrast to multiple sclerosis, where advancing age and older onset are associated with reduced relapse activity, allowing for treatment de-escalation or discontinuation in some older patients. The aim of this study was to clarify the influence of age at onset on relapse risk as well as disability accrual in a large, international cohort of patients with NMOSD. Methods We conducted a retrospective, multicenter cohort study using the MSBase data registry to evaluate annualized relapse rates (ARRs), time to first relapse, and time to Expanded Disability Status Scale (EDSS) scores of 4 and 6. For inclusion, a diagnosis of AQP4-IgG NMOSD according to the latest iteration of the criteria and availability of the minimum data set were required. Patients were stratified as pediatric onset (<18 years of age), early onset (18-55 years inclusive) or late onset (>55 years of age). Analyses included patients on high-efficacy therapy (HET), those on low-efficacy therapy (LET), and an incident cohort with the first clinical visit within 12 months from disease onset. Predictors of first relapse and EDSS 4/6 thresholds were analyzed using Cox proportional models. Results Data from 539 patients (42 pediatric, 421 with early onset, 76 with late onset
dc.description.abstract85.2% female) with a median age at onset of 35 years (Q1 25.10, Q3 47.60) and a disease duration of 7.42 years (Q1 3.23, Q3 13.10) were analyzed. ARR and time to first relapse were not influenced by age at disease onset. Patients on HET had fewer relapses than those on LET (p < 0.001). Older age was linked to faster disability accumulation. In addition, higher baseline EDSS scores and delayed treatment were independent predictors of future disability. Discussion Our study demonstrates that while age at onset does not affect relapse risk, older patients experience more rapid disability accrual. These findings underscore the importance of early initiation of effective preventive immunotherapy in all age groups. The primary limitations of this study pertain to its retrospective design and the sole reliance on EDSS for disability assessment.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionPublished Version
dc.identifier.WoSQuartileQ1
dc.identifier.doi10.1212/WNL.0000000000214707
dc.identifier.eissn1526-632X
dc.identifier.embargoNo
dc.identifier.issn0028-3878
dc.identifier.issue7
dc.identifier.pubmed41785437
dc.identifier.scopus2-s2.0-105032342070
dc.identifier.urihttps://doi.org/10.1212/WNL.0000000000214707
dc.identifier.urihttps://hdl.handle.net/20.500.14288/33037
dc.identifier.volume106
dc.identifier.wos001707898300001
dc.keywordsAquaporin-4 antibody NMOSD
dc.keywordsAge at onset
dc.keywordsRelapse risk
dc.keywordsDisability accrual
dc.keywordsMSBase registry
dc.keywordsHigh-efficacy therapy
dc.keywordsLow-efficacy therapy
dc.keywordsExpanded Disability Status Scale
dc.languageeng
dc.publisherLippincott Williams and Wilkins
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofNeurology
dc.relation.openaccessN/A
dc.rightsN/A
dc.rights.uriN/A
dc.subjectClinical neurology
dc.titleImpact of age at onset on relapse and disability in AQP4-IgG neuromyelitis optica spectrum disorder
dc.typeJournal Article
dspace.entity.typePublication
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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