Evidence map›Paper›PMID 40267375›Full record

Observational studyNeurology2025

Multiple Sclerosis-Specific Reference Curves for Brain Volumes to Explain Disease Severity.

David Rudolf van Nederpelt, Lonneke Bos, Rozemarijn M Mattiesing, Eva M M Strijbis, Bastiaan Moraal, Joost Kuijer, Jeroen Hoogland, Henk J M M Mutsaerts, Bernard Uitdehaag, Joep Killestein and 5 more

Erratum issuedAbstract readObservational 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. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

David Rudolf van NederpeltMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.
Lonneke BosMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.
Rozemarijn M MattiesingMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.
Eva M M StrijbisMS Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.ORCID 0000-0001-6705-5864
Bastiaan MoraalMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.
Joost KuijerMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.
Jeroen HooglandDepartment of Epidemiology and Data Science, Amsterdam UMC, the Netherlands.ORCID 0000-0002-2397-6052
Henk J M M MutsaertsMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.ORCID 0000-0003-0894-0307
Bernard UitdehaagMS Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.ORCID 0000-0002-9226-7364
Joep KillesteinMS Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.ORCID 0000-0002-6347-5957
Lizette HeineQuantib B.V., DeepHealth, Rotterdam, the Netherlands.ORCID 0000-0003-1369-8199
Bas JasperseMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.
Frederik BarkhofMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.ORCID 0000-0003-3543-3706
Menno M SchoonheimMS Center Amsterdam, Anatomy and Neurosciences, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.ORCID 0000-0002-2504-6959
Hugo VrenkenMS Center Amsterdam, Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands.ORCID 0000-0001-9106-1172

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesBrain atrophy is relevant for understanding disease progression and treatment response in people with multiple sclerosis (pwMS). Automatic brain volume-reporting tools often rely on healthy control (HC) reference curves to interpret brain volumes, whereas brain volume loss is different in pwMS. This observational study aimed to develop an MS-specific reference model for brain volumes and evaluate its performance compared with HC-based curves, as a proof-of-concept.

methodsParticipants, pwMS and HCs, from the Amsterdam MS cohort were included based on the availability of T1-weighted MR scans. Normalized brain volumes (NBVs) were obtained using commercially available software. The software program also provides NBV percentiles, based on age-specific and sex-specific HC curves, grouped into NBV quartiles, describing deviation from expected NBVs. Disease severity was determined with the MS severity score (MSSS), Symbol Digit Modalities Test (SDMT), and 9-Hole Peg Test (9HPT). An MS-specific model was developed by regressing NBVs against age, sex, disease duration, and MS phenotype. The resulting MS model was also used to classify pwMS into quartiles describing deviation from expected NBV, given the modeled patient characteristics, with leave-one-out predictions. Quartile classification from HC-based and MS-based reference curves was compared with MSSS using analysis of variance (ANOVA).

resultsRegressions for NBVs from 713 pwMS and 259 HCs (mean age: 49.1 ± 9.7 and 48.3 ± 10.1, %female: 70.4% and 67.2%, respectively) were significant for age, sex, disease duration, and phenotype, which were included in the MS-specific model. MS-specific model quartile designations significantly improved associations with MSSS values ( DISCUSSION: NBV values derived from an MS-specific reference model offer improved relevance for assessing disease severity compared with curves derived from age-specific and sex-specific HC reference models. Improving the model toward application in individual people could enhance clinical implementation.

Indexed as

BrainMultiple SclerosisAdultAtrophyCohort StudiesDisease ProgressionFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedOrgan SizeReference ValuesSeverity of Illness Index

Identifiers

PMID40267375
PMCPMC12012623

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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.