Evidence map›Paper›PMID 41252657›Full record

ArticleNeurology(R) neuroimmunology & neuroinflammation2026

Spinal Cord Leptomeningeal Enhancement as a Marker of Extensive Spinal Cord Involvement in Children With MOGAD.

Serenella Bartiromo, Cesar Alves, Julia O'Mahony, E Ann Yeh, Ruth Ann Marrie, Sridar Narayanan, Patrick J Waters, Alberto Gajofatto, Amit Bar-Or, Brenda L Banwell and 2 more

Abstract read
In one paragraph

Article in Neurology(R) neuroimmunology & neuroinflammation, 2026. 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

12 authors.

Serenella BartiromoDepartment of Medicine, University of Ottawa, Ottawa Hospital Research Institute, Canada.
Cesar AlvesDepartment of Radiology, Division of Neuroradiology, Boston Children's Hospital- BCH, Harvard Medical School, MA.ORCID 0000-0001-5877-9086
Julia O'MahonyMellen Center for Multiple Sclerosis, Cleveland Clinic Foundation, OH.ORCID 0000-0001-8338-1133
E Ann YehDivision of Neurology, Department of Pediatrics, Hospital for Sick Children, Program in Neurosciences and Mental Health, SickKids Research Institute, University of Toronto, ON, Canada.ORCID 0000-0002-5393-7417
Ruth Ann MarrieDepartment of Medicine, Dalhousie University, Halifax, Canada.ORCID 0000-0002-1855-5595
Sridar NarayananMcConnell Brain Imaging Centre, Montreal Neurological Institute-Hospital, McGill University, Montreal, Canada.ORCID 0000-0002-6283-150X
Patrick J WatersNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, United Kingdom.ORCID 0000-0003-4142-2667
Alberto GajofattoDepartment of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Italy.ORCID 0000-0001-6539-0458
Amit Bar-OrCenter for Neuroinflammation and Neurotherapeutics, and Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia; and.ORCID 0000-0001-7179-0335
Brenda L BanwellDepartment of Pediatrics, Johns Hopkins University, Baltimore, MD.ORCID 0000-0001-6354-6770
Giulia FaddaDepartment of Medicine, University of Ottawa, Ottawa Hospital Research Institute, Canada.
Canadian Pediatric Demyelinating Disease Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesSpinal cord leptomeningeal enhancement (LME) can be observed in children with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and with seronegative myelitis. We investigated whether the presence of spinal cord LME in MOGAD and seronegative myelitis is associated with distinct clinical, CSF, and MRI findings.

methodsStudy participants were identified among the 490 children and adolescents recruited to the Canadian Pediatric Demyelinating Disease study following an incident attack of CNS demyelination. Inclusion criteria for this study were: (1) evidence of spinal cord lesions on MRI, (2) available postgadolinium MRI sequences, and (3) available MOG and aquaporin-4 (AQP4) antibody results. None of the AQP4 antibody-positive participants met our inclusion criteria and only 1 participant with multiple sclerosis exhibited LME. We therefore focused the study on children with MOGAD and seronegative myelitis and compared the clinical, CSF, and MRI features between participants with and without LME.

resultsOur cohort included 33 participants with MOGAD (median age 5.9 years, 55% women) and 45 with seronegative myelitis (median age 11.9 years, 33% women). Spinal cord LME was detected in 20/33 (61%) participants with MOGAD and 14/45 (31%) with seronegative myelitis. Among children with MOGAD, those with LME were more likely than those without LME to have longitudinally extensive myelitis ([LETM], 19/20 vs 8/13, DISCUSSION: The presence of spinal cord LME is associated with more extensive spinal cord abnormalities on MRI in children with MOGAD and to a lesser extent in those with seronegative myelitis. The biological underpinnings of this finding and its clinical implications should be assessed in further studies.

Indexed as

Demyelinating Autoimmune Diseases, CNSMeningesMyelin-Oligodendrocyte GlycoproteinMyelitisSpinal CordAdolescentAutoantibodiesChildChild, PreschoolFemaleHumansMagnetic Resonance ImagingMaleMyelin Oligodendrocyte Glycoprotein Antibody-Associated DiseaseAutoantibodiesMyelin-Oligodendrocyte Glycoprotein

Identifiers

PMID41252657
PMCPMC12631794

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LicenceCC BY-NC-ND
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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.