Evidence map›Paper›PMID 41254968›Full record

ArticleEuropean journal of neurology2025

Longitudinal Brain Atrophy Patterns in Early MOG-Antibody Associated Disease and Relapsing Multiple Sclerosis.

Theodoros Ladopoulos, David Bratek, Carolin Schwake, Ann-Kathrin Kogel, Barbara Bellenberg, Britta Krieger, Zainab Abbas, Ralf Gold, Carsten Lukas, Ilya Ayzenberg and 1 more

Abstract read
In one paragraph

Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Theodoros LadopoulosDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.ORCID 0009-0006-1735-4130
David BratekDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.
Carolin SchwakeDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.
Ann-Kathrin KogelDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.ORCID 0000-0002-8217-6063
Barbara BellenbergInstitute for Neuroradiology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.
Britta KriegerInstitute for Neuroradiology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.ORCID 0000-0002-6364-2743
Zainab AbbasDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.
Ralf GoldDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.
Carsten LukasDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.
Ilya AyzenbergDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.
Ruth SchneiderDepartment of Neurology, St Josef Hospital, Ruhr University Bochum, Bochum, Germany.

Funding

Bundesministerium für Bildung und Frauen 01GI0914KKNMS 01GI1601I
6 · The paper itself

Abstract

backgroundMyelin oligodendrocyte glycoprotein antibody-associated disease can manifest as a relapsing or monophasic condition. Although several MRI studies have shown evident gray and white matter atrophy compared to healthy controls, little is known about regional brain volume dynamics in myelin oligodendrocyte glycoprotein antibody-associated disease over time.

methodsIn this study, we performed an explorative voxel-based morphometry to detect brain volumetric differences between myelin oligodendrocyte glycoprotein antibody-associated disease (N = 27), relapsing multiple sclerosis (N = 40)-both in early disease stages-and healthy controls (N = 45). Furthermore, we investigated the longitudinal brain volume changes over a 2-year follow-up period in myelin oligodendrocyte glycoprotein antibody-associated disease (N = 15) and relapsing multiple sclerosis (N = 40).

resultsWe identified distinct patterns of regional brain volume loss in the patient subgroups compared to healthy controls. In multiple sclerosis patients, bilateral thalamic atrophy was observed, whereas patients with myelin oligodendrocyte glycoprotein antibody-associated disease showed atrophy of the bilateral fornix and stria terminalis. Our results confirmed longitudinal volume loss in thalamic and infratentorial regions in the relapsing multiple sclerosis group, which was partly related to clinical relapses during the 2-year follow-up period. In contrast, no longitudinal gray or white matter changes were found in the myelin oligodendrocyte glycoprotein antibody-associated disease group.

conclusionsTo our knowledge, this is the first MRI study demonstrating no evidence of regional brain volume loss over time in patients with myelin oligodendrocyte glycoprotein antibody-associated disease using voxel-based morphometry, suggesting a different-probably not progressive-pathophysiological background compared to relapsing multiple sclerosis.

Indexed as

BrainMagnetic Resonance ImagingMultiple Sclerosis, Relapsing-RemittingMyelin Oligodendrocyte Glycoprotein Antibody-Associated DiseaseAdultAtrophyCase-Control StudiesCross-Sectional StudiesDisease ProgressionFemaleFollow-Up StudiesHumansLongitudinal StudiesMaleOrgan SizeRetrospective Studiesbrain atrophyMOGADMRIprogressionRRMSvoxel‐based morphometry

Identifiers

PMID41254968
PMCPMC12627754

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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.