Evidence map›Paper›PMID 42005248›Full record

ArticleCureus2026

Highly Aggressive Relapsing Course of Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-Associated Disease Requiring Intensive Care Unit Treatment and Quadruple Immunotherapy.

Deepak Sharma, Wiebke Böhmer, Christian P Kamm, Lara Diem

Abstract readCase Reports
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Deepak SharmaNeurology, Luzerner Kantonsspital, Luzern, CHE.
Wiebke BöhmerNeurology, Klinik Lengg, Zürich, CHE.
Christian P KammNeurology, Luzerner Kantonsspital, Luzern, CHE.
Lara DiemNeurology, Luzerner Kantonsspital, Luzern, CHE.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an autoimmune-mediated demyelinating disorder of the central nervous system (CNS). Clinical manifestations and disease courses range from involvement of the optic nerve, spinal cord, or brainstem to acute disseminated encephalomyelitis (ADEM), and from monophasic to relapsing or progressive forms. Diagnosis can be challenging; repeated testing is sometimes required to establish the diagnosis, particularly in atypical clinical presentations. First-line therapy in the acute setting consists of corticosteroids, whereas steroid-sparing agents are used for long-term management in relapsing cases. Various therapeutic strategies, particularly in aggressive courses, have been described in case reports. We report a challenging case of a 34-year-old woman with a severe relapsing disease course requiring intensive care unit (ICU) support. Anti-myelin oligodendrocyte glycoprotein-immunoglobulin G (anti-MOG IgG) was detected only after repeated testing using different assays. Brain biopsy identified an unidentified viral pathogen of uncertain clinical relevance. The disease demonstrated marked refractoriness to standard therapies.

Indexed as

delayed seroconversioniviglive-cell binding assaymogadmog antibody-associated diseasequadruple immunotherapyrituximabtocilizumabtreatment-refractory demyelination

Identifiers

PMID42005248
PMCPMC13086862

What OpenQuestion holds

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Registered trials

None linked

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.