Evidence map›Paper›PMID 42632831›Full record

SynthesisJournal of neurology2026

Central vein sign and paramagnetic rim lesions in pediatric-onset multiple sclerosis: a systematic review and meta-analysis.

Anna de Mauro, Rosa Cortese, Giulia Fadda, Nicola De Stefano, Ludwig Kappos, Maria Pia Sormani, Brenda Banwell, Cristina Granziera, Alessandro Cagol

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis 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.

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

9 authors.

Anna de MauroTranslational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Faculty of Medicine, University Hospital Basel and University of Basel, Basel, Switzerland.
Rosa CorteseTranslational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Faculty of Medicine, University Hospital Basel and University of Basel, Basel, Switzerland.
Giulia FaddaDepartment of Medicine, University of Ottawa, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Nicola De StefanoDepartment of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.
Ludwig KapposTranslational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Faculty of Medicine, University Hospital Basel and University of Basel, Basel, Switzerland.
Maria Pia SormaniDipartimento Di Scienze Della Salute, Università Degli Studi Di Genova, Genoa, Italy.
Brenda BanwellDepartment of Pediatrics, Johns Hopkins University, Baltimore, MD, USA.
Cristina Granziera *Translational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Faculty of Medicine, University Hospital Basel and University of Basel, Basel, Switzerland. cristina.granziera@usb.ch.ORCID http://orcid.org/0000-0002-4917-8761
Alessandro Cagol *Translational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Faculty of Medicine, University Hospital Basel and University of Basel, Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSusceptibility-based MRI biomarkers, including paramagnetic rim lesions (PRLs) and central vein sign (CVS), were incorporated into the 2024 McDonald criteria because they improve diagnostic specificity in adult-onset MS; however, their role in pediatric-onset MS (POMS) remains incompletely defined.

objectiveTo synthesize current evidence on the prevalence and diagnostic value of PRLs and CVS in POMS.

methodsWe conducted a PRISMA-compliant systematic review and random-effects meta-analysis of studies reporting PRLs and/or CVS in POMS. Outcomes included the proportion of patients with ≥1 PRL, the mean proportion of CVS-positive lesions, and fulfillment of CVS-based thresholds.

resultsEleven studies were included. Across seven studies, the pooled proportion of POMS patients with ≥1 PRL was 71.6% (95% CI 61.1-80.2; n=149), with low between-study heterogeneity. Across six studies, the pooled mean proportion of CVS-positive lesions was 57.9% (95% CI 39.7-76.2; n=99), and 66.2% (95% CI 10.5-97.0; n=219) of patients fulfilled the 40%-CVS rule, with substantial variability across studies. In comparative analyses, PRLs showed high specificity for POMS, while CVS was more prevalent than in mimics; however, limited data precluded quantitative evaluation.

conclusionPRLs are frequent in POMS. Limited comparative data suggest that PRLs may have high diagnostic specificity, whereas CVS appears more variable; however, pediatric diagnostic accuracy evidence remains scarce. Further pediatric-specific studies are needed to define the optimal diagnostic use of these biomarkers in POMS.

Indexed as

Magnetic Resonance ImagingMultiple SclerosisChildHumans2024 McDonald criteriaCVSDifferential diagnosisPOMSPRL

Identifiers

PMID42632831
PMCPMC13499817

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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.