Evidence map›Paper›PMID 41100780›Full record

Observational studyNeurology2025

Multiple Sclerosis Relapse Treatment During Pregnancy and Offspring Functional and Structural Neurodevelopment: A Cross-Sectional Study.

Valeska Kozik, Michelle Dreiling, Denise Müller, Oliver Tiedge, Ruth Schneider, Sandra Thiel, Barbara Bellenberg, Britta Krieger, Carsten Lukas, Hans-Joachim Mentzel and 4 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Neurology, 2025. 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

14 authors.

Valeska KozikDepartment of Neurology, Jena University Hospital, Germany.ORCID 0000-0002-7895-6788
Michelle DreilingDepartment of Neurology, Jena University Hospital, Germany.
Denise MüllerDepartment of Neurology, Jena University Hospital, Germany.
Oliver TiedgeNeuroZentrum Erfurt, Private Practice, Germany.
Ruth SchneiderDepartment of Neurology, St. Josef Hospital, Ruhr University Bochum, Germany.ORCID 0000-0002-0997-2725
Sandra ThielDepartment of Neurology, St. Josef Hospital, Ruhr University Bochum, Germany.ORCID 0000-0002-5113-8451
Barbara BellenbergInstitute of Neuroradiology, St. Josef Hospital, Ruhr University Bochum, Germany.ORCID 0000-0001-7484-6787
Britta KriegerInstitute of Neuroradiology, St. Josef Hospital, Ruhr University Bochum, Germany.ORCID 0000-0002-6364-2743
Carsten LukasInstitute of Neuroradiology, St. Josef Hospital, Ruhr University Bochum, Germany.ORCID 0000-0002-8562-9697
Hans-Joachim MentzelDepartment of Diagnostic and Interventional Radiology, Jena University Hospital, Germany.
Christian GaserDepartment of Neurology, Jena University Hospital, Germany.
Kerstin HellwigDepartment of Neurology, St. Josef Hospital, Ruhr University Bochum, Germany.ORCID 0000-0003-4467-9011
Matthias SchwabDepartment of Neurology, Jena University Hospital, Germany.
Florian RakersDepartment of Neurology, Jena University Hospital, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesHigh-dose methylprednisolone (MP) is the global standard for treating pregnancy-associated relapses in multiple sclerosis (MS). Given that glucocorticoids cross the placenta and may interfere with fetal brain development, concerns remain about their long-term safety. This study assessed whether in utero MP exposure as part of MS relapse therapy affects neurodevelopment in school-aged children.

methodsIn this cross-sectional, 2-center study, term-born children with prenatal exposure to MP due to maternal MS relapse treatment were compared with a nonexposed reference group of children, all born to mothers with MS. Participants were primarily identified using the German MS and Pregnancy Registry and assessed at tertiary MS centers. The primary outcome was global cognitive ability, measured using a standardized intelligence test. Secondary outcomes included attention, behavior, motor performance, and electrocortical activity at rest. Structural brain development was assessed using high-resolution MRI, including voxel-based and surface-based morphometry. Deviations from chronological brain age were quantified using a machine learning-based framework. Statistical associations were examined using linear regression models.

resultsThe MP-exposed group (n = 30; mean age 9.6 years; 37% female) and the reference group (n = 30; mean age 10.0 years; 40% female) were comparable with respect to demographic and perinatal characteristics. The median cumulative MP dose was 5 g (Q1-Q3: 3-7.5), predominantly administered during the second trimester. Global IQ did not differ between groups (MP: 103.0; 95% CI: 99.2-106.8 vs reference: 101.5; 95% CI: 97.6-105.3). After correction for multiple comparisons, no group differences emerged in secondary neuropsychological outcomes or electrocortical parameters. MRI analyses revealed no differences in gray matter volume, cortical thickness, gyrification, or chronological brain age. DISCUSSION: In spite of theoretical concerns that MP exposure during pregnancy might lead to alterations in neurodevelopment, this was not found to be the case in this cohort, with most exposures occurring during the second trimester. However, this study was not powered to detect subtle associations in secondary analyses or to draw definitive conclusions regarding potential dose-response relationships. Given the remaining uncertainties, MP should be used with caution at the lowest effective dose until larger follow-up studies provide further clarity.

Indexed as

BrainChild DevelopmentMethylprednisoloneMultiple SclerosisPregnancy ComplicationsPrenatal Exposure Delayed EffectsAdultChildCross-Sectional StudiesFemaleHumansMagnetic Resonance ImagingMalePregnancyRecurrenceMethylprednisolone

Identifiers

PMID41100780
PMCPMC12533490

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Registered trials

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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.