Evidence map›Paper›PMID 41870604›Full record

ArticleJournal of neurology2026

Prediction of relapse in myelin oligodendrocyte glycoprotein antibody-associated disease: external validation of the MOG-AR score.

Wei Zhen Yeh, Anna Francis, Helmut Butzkueven, Ruth Geraldes, Maria Isabel Leite, Jacqueline Palace

Abstract readValidation Study
In one paragraph

Article in Journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Wei Zhen YehNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK. wei.yeh@monash.edu.ORCID http://orcid.org/0000-0002-5335-6612
Anna FrancisNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Helmut ButzkuevenDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Australia.
Ruth GeraldesNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Maria Isabel LeiteNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Jacqueline PalaceNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK. jacqueline.palace@ndcn.ox.ac.uk.

Funding

Multiple Sclerosis Australia 24-PDF-0166
6 · The paper itself

Abstract

backgroundPredicting relapses in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) when disability is relapse-dependent is crucial to guide treatment decisions including whether to treat from onset. MOG-AR, a relapse risk score, was recently developed in a Chinese cohort from disease onset. This study aimed to externally validate the MOG-AR score.

methodsMOGAD patients seen through the Oxford National NMO Service with ≥ 1-year disease duration and available data for MOG-AR score calculation (variables of age, sex, onset attack phenotype, treatment) were included. MOG-AR score and grade were calculated. Relapse occurrence at 3 years from onset was used as the primary outcome. MOG-AR performance was assessed by measures of discrimination and calibration.

resultsWe included 284 MOGAD patients with a 4.7-year median disease duration. Relapse occurred in 38% within 3 years of onset. Median MOG-AR score and grade were 11 (IQR 10-12) and 3 (3-3) for those who relapsed and 9 (8-11) and 3 (2-3) for those who did not. Observed proportion with relapse was 27%, 26%, 41%, and 53% for grades 1, 2, 3, and 4, respectively. Discrimination assessment by grade showed an area under the receiver operating characteristic curve of 0.58 (95% CI 0.52-0.63). Calibration assessment was consistent with overestimation of relapse probabilities.

conclusionIn a UK-MOGAD cohort, MOG-AR score showed suboptimal performance in predicting relapse over a 3-year period from onset. Further work to find clinically accessible predictive biomarkers and tools for a relapsing course would facilitate better treatment strategies near disease onset.

Indexed as

Myelin-Oligodendrocyte GlycoproteinMyelin Oligodendrocyte Glycoprotein Antibody-Associated DiseaseAdultFemaleHumansMaleMiddle AgedRecurrenceSeverity of Illness IndexMyelin-Oligodendrocyte GlycoproteinMOGADMyelin oligodendrocyte glycoprotein antibody-associated diseasePredictionRelapseRisk scoreValidation

Identifiers

PMID41870604
PMCPMC13009136

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.