Evidence map›Paper›PMID 41180519›Full record

ArticleFrontiers in neurology2025

Real-world brain volumetry in multiple sclerosis: importance of methodological consistency and clinical relevance of gray matter atrophy.

Joke Temmerman, Ann Vanremoortel, Maria Bjerke, Marie B D'Hooghe, Guy Nagels, Ayla Pauwels, Diana Sima, Dirk Smeets, Jeroen Van Schependom, Mandy M J Wittens and 2 more

Abstract read
In one paragraph

Article in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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

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.

Joke TemmermanVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Ann VanremoortelNationaal Multiple Sclerose Centrum, Melsbroek, Belgium.
Maria BjerkeVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Marie B D'HoogheVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Guy NagelsVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Ayla PauwelsVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Diana SimaVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Dirk SmeetsVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Jeroen Van SchependomVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Mandy M J WittensVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Sebastiaan EngelborghsVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.
Miguel D'haeseleerVrije Universiteit Brussel, Center for Neurosciences, NEUR and/or AIMS Research Groups, Brussels, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Brain volume loss (BVL) is a marker of neurodegeneration associated with clinical disability in multiple sclerosis (MS). However, its application in routine clinical practice is limited due to measurement errors introduced by the use of different magnetic resonance imaging (MRI) scanners across and within centers. Objective: To confirm the existence and clinical relevance of longitudinal BVL in a real-world MS cohort with scanner variability, employing a dedicated quantification pipeline combined with post-acquisition harmonization. Methods: We analyzed MRI data from 72 MS patients scanned across multiple Belgian centers over 48-60 months. Clinical disability was assessed using the Expanded Disability Status Scale, Timed 25-Foot Walk Test, 9-Hole Peg Test (9HPT), and Symbol Digit Modalities Test. Percentage volume change (PVC) in whole brain (WB), total gray matter (TGM), cortical gray matter (CGM), and deep gray matter was quantified using the icobrain ms pipeline. A similarity index was applied to account for scanner differences. Twenty-seven healthy volunteers served as controls. Results: No significant differences in annualized PVC were observed between MS patients and controls. Within the MS group, 9HPT performance correlated with TGM ( Conclusion: Using automated brain volumetry with post-acquisition harmonization to address scanner variability, we did not detect accelerated BVL in this real-world MS cohort compared to healthy individuals. Nonetheless, GM volume loss was found to be clinically relevant in MS.

Indexed as

brain volume lossdisability progressiongray mattermultiple sclerosispost-acquisition harmonizationreal-world

Identifiers

PMID41180519
PMCPMC12571658

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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.