ArticleFrontiers in neurology2025
Real-world brain volumetry in multiple sclerosis: importance of methodological consistency and clinical relevance of gray matter atrophy.
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.
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.
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.
Who cites it
3 citing papers in PubMed.
- Clinical trials in non-ambulatory people with progressive multiple sclerosis: can the nine hole peg test step up as primary outcome measure?Journal of neurology · 2026Article
- Spinal cord reserve is associated with multi-dimensional clinical resilience in multiple sclerosis.Journal of neurology · 2026Article
- AI-Based Brain Volumetry Without MPRAGE? Evaluation of Synthetic T1-MPRAGE from 2D T2/FLAIR.Diagnostics (Basel, Switzerland) · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
Registered trials
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.