Evidence map›Paper›PMID 42307802›Full record

ArticleJournal of neurology2026

Spinal cord reserve is associated with multi-dimensional clinical resilience in multiple sclerosis.

Stien Willems, Marie B D'hooghe, Jaume Sastre-Garriga, Deborah Pareto, Diana M Sima, Neus Mongay-Ochoa, Laetitia Della Faille, Arno Liseune, Guy Nagels, Ann Van Remoortel and 2 more

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Article 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

12 authors.

Stien WillemsNational Multiple Sclerosis Center, Vanheylenstraat 16, 1820, Melsbroek, Belgium.ORCID http://orcid.org/0009-0002-1144-0944
Marie B D'hoogheNational Multiple Sclerosis Center, Vanheylenstraat 16, 1820, Melsbroek, Belgium.
Jaume Sastre-GarrigaCentre d'Esclerosi Múltiple de Catalunya (Cemcat), Department of Neurology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Deborah ParetoNeuroradiology Section, Department of Radiology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Diana M SimaIcometrix, Leuven, Belgium.
Neus Mongay-OchoaCentre d'Esclerosi Múltiple de Catalunya (Cemcat), Department of Neurology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Laetitia Della FailleNational Multiple Sclerosis Center, Vanheylenstraat 16, 1820, Melsbroek, Belgium.
Arno LiseuneIcometrix, Leuven, Belgium.
Guy NagelsDepartment of Neurology, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Ann Van RemoortelNational Multiple Sclerosis Center, Vanheylenstraat 16, 1820, Melsbroek, Belgium.
Jeroen Van SchependomNEUR Research Group, Center for Neurosciences, Vrije Universiteit Brussel, Brussels, Belgium.
Miguel D'HaeseleerNational Multiple Sclerosis Center, Vanheylenstraat 16, 1820, Melsbroek, Belgium. miguel.dhaeseleer@mscenter.be.ORCID http://orcid.org/0000-0003-4378-0089

Funding

Innovative Health Initiative 101112153Merck Donation for Patient Benefit
6 · The paper itself

Abstract

objectiveSpinal canal area (SCaA)-a proxy for maximal lifetime spinal cord growth-has recently been associated with concurrent disability and future worsening in multiple sclerosis (MS). Prior studies focused mainly on the Expanded Disability Status Scale (EDSS). This study evaluates whether SCaA also relates to broader clinical outcomes.

methodsWe performed a retrospective longitudinal study at the Belgian National MS Center. SCaA and spinal cord area (SCoA) were quantified on 714 brain MRI scans from 426 patients with MS using newly developed deep learning models. Two approaches were applied at C2-C3: averaging values across the entire spinal segment (method 1) or across 10 slices centered on the intervertebral disc (method 2). Disability measures included the EDSS, Timed 25‑Foot Walk Test (T25FWT), 9‑Hole Peg Test (9HPT), and Symbol Digit Modalities Test (SDMT). Associations of SCaA with concurrent disability and longitudinal change were assessed using multivariable regression.

resultsMean SCaA and SCoA were 209.6 ± 32.9 mm

conclusionSmaller SCaA is associated with greater clinical disability and future deterioration across multiple functional domains in MS. Our findings support the emerging concept of spinal cord reserve.

Indexed as

Multiple SclerosisSpinal CordAdultDisability EvaluationDisease ProgressionFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMiddle AgedRetrospective StudiesMagnetic resonance imagingMultiple sclerosisReserveSpinal canal area

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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.