ArticleJournal of neurology2025
MOG-IgG detection in serum and cerebrospinal fluid: diagnostic implications and clinical correlates in adult-onset Chinese MOGAD patients.
Article in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.
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Who cites it
3 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Global trends and research hotspots in autoimmune encephalitis: insights from a bibliometric and visualized analysis: 1971-2025.Frontiers in immunology · 2026Pooled it
- From the Optic Neuritis Treatment Trial to Antibody-Mediated Optic Neuritis: Four Decades of Progress and Unanswered Questions.Biomedicines · 2026Review
- The relationship between serum MOG-IgG titer status and titers and the prognosis of pediatric MOGAD: a retrospective cohort study.Frontiers in pediatrics · 2026Article
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveTo assess the diagnostic significance and clinical features of cerebrospinal fluid (CSF)-restricted MOG-IgG in Chinese adults with MOG-IgG-associated disease (MOGAD), and to compare phenotypes across MOG-IgG statuses and ethnicities.
methodsEighty-two adults with suspected inflammatory demyelinating diseases and positive MOG-IgG (serum and/or CSF) were retrospectively analyzed from 2014 to 2024. Patients were categorized into two groups based on MOG-IgG status: MOG-IgG Seropositive group (MOG-IgG Seropositive and CSF Negative) and CSF Positive group (MOG-IgG paired serum and CSF positive, CSF-restricted MOG-IgG). Clinical, radiological, and therapeutic features were evaluated. Logistic regression was used to identify predictors of poor prognosis. Literatures on CSF-restricted MOG-IgG in different ethnicities were reviewed.
resultsSix patients (7.3%) had CSF-restricted MOG-IgG, and 83.3% met MOGAD phenotypes. Optic neuritis was the most common presentation (54.8%), followed by cerebral cortical encephalitis and acute disseminated encephalomyelitis. Visual and motor impairments at onset were more frequent in the seropositive group. Independent risk factors for EDSS ≥ 3.0 included higher nadir EDSS score (OR: 2.39), visual impairment (OR: 10.94), and brainstem dysfunction (OR: 8.75).
conclusionsCSF-restricted MOG-IgG defines a distinct MOGAD subgroup, supporting its diagnostic relevance. Visual and brainstem involvement predict worse outcomes. Larger, multiethnic prospective studies are warranted to refine diagnostic thresholds and clarify the role of intrathecal antibody production.
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