Evidence map›Paper›PMID 40924955›Full record

ArticleNeurology(R) neuroimmunology & neuroinflammation2025

Relation of Visual Function, Retinal Thickness by Optical Coherence Tomography, and MRI Brain Volume in Pediatric-Onset Multiple Sclerosis.

Anna Sosa, Kimberly A O'Neill, Ruben Jauregui, Ugo Nwigwe, Thibo Billiet, Rachel Kenney, Lauren B Krupp, Steven L Galetta, Laura J Balcer, Scott N Grossman

Abstract read
In one paragraph

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

10 authors.

Anna SosaDepartment of Neurology, NYU Grossman School of Medicine, NY.ORCID 0009-0008-7752-2532
Kimberly A O'NeillDepartment of Neurology, NYU Grossman School of Medicine, NY.
Ruben JaureguiDepartment of Neurology, NYU Grossman School of Medicine, NY.ORCID 0000-0002-2367-7298
Ugo NwigweDepartment of Neurology, NYU Grossman School of Medicine, NY.ORCID 0009-0005-6485-1386
Thibo BillietIcometrix, Leuven, Belgium.ORCID 0000-0002-3248-5044
Rachel KenneyDepartments of Neurology and Population Health, NYU Grossman School of Medicine, NY.ORCID 0000-0003-1311-5520
Lauren B KruppDepartment of Neurology, NYU Grossman School of Medicine, NY.ORCID 0000-0001-7003-807X
Steven L GalettaDepartments of Neurology and Ophthalmology, NYU Grossman School of Medicine, NY; and.ORCID 0000-0003-3781-7324
Laura J BalcerDepartments of Neurology, Ophthalmology and Population Health, NYU Grossman School of Medicine, NY.ORCID 0000-0002-5136-4539
Scott N GrossmanDepartments of Neurology and Ophthalmology, NYU Grossman School of Medicine, NY; and.ORCID 0000-0001-7033-5226

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesWhile reductions in optical coherence tomography (OCT) pRNFL and ganglion cell-inner plexiform layer thicknesses have been shown to be associated with brain atrophy in adult-onset MS (AOMS) cohorts, the relationship between OCT and brain MRI measures is less established in pediatric-onset MS (POMS). Our aim was to examine the associations of OCT measures with volumetric MRI in a cohort of patients with POMS to determine whether OCT measures reflect CNS neurodegeneration in this patient population, as is seen in AOMS cohorts.

methodsThis was a cross-sectional study with retrospective ascertainment of patients with POMS evaluated at a single center with expertise in POMS and neuro-ophthalmology. As part of routine clinical care, patients with POMS are evaluated by a POMS expert and undergo volumetric brain MRI, including whole-brain (WB), subregional, and gray matter (GM) volume analyses. Patients with POMS are routinely referred to neuro-ophthalmology for evaluation that includes high-contrast visual acuity, color vision testing, and OCT. Generalized estimating equation (GEE) models, accounting for within-patient, intereye correlations (both eyes of each patient were included), MS disease duration, and disease-modifying therapy efficacy, were used to determine the relationship between visual pathway structure and function and volumetric MRI measures.

resultsAmong 61 patients (122 eyes) with POMS, the mean age at the time of the volumetric MRI scan was 19.2 (SD = 3.7, range 10-27) years, with a median disease duration of 2.8 (range 0-14) years. Lower (worse) pRNFL thicknesses (mean 87.4 [17.2] µm) were associated with reduced volume percentiles of WB ( DISCUSSION: Our results demonstrate that changes in visual pathway structures are associated with reductions in overall brain volume and GM volumes, as well as greater lesion and black hole burden. Collectively, our results emphasize the importance of visual assessment in POMS and suggest that OCT reflects overall CNS neurodegeneration in this cohort.

Indexed as

BrainMultiple SclerosisRetinaAdolescentAdultChildCross-Sectional StudiesFemaleHumansMagnetic Resonance ImagingMaleRetrospective StudiesTomography, Optical CoherenceVisual AcuityYoung Adult

Identifiers

PMID40924955
PMCPMC12424074

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