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Updated: Jun 2, 2026

08:51
Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla
Published on: February 19, 2021
Longitudinal gray matter changes in multiple sclerosis--differential scanner and overall disease-related effects
Kerstin Bendfeldt1, Louis Hofstetter, Pascal Kuster
1Medical Image Analysis Center, University Hospital Basel, CH-4031 Basel, Switzerland.
Human Brain Mapping
|May 4, 2011
Summary
Voxel-based morphometry (VBM) can reliably detect gray matter atrophy in multiple sclerosis (MS) across different MRI scanners. This study shows scanner variations have minimal impact, allowing data pooling for robust multi-center MS research.
Area of Science:
- Neuroimaging
- Neurology
- Medical Imaging Analysis
Background:
- Voxel-based morphometry (VBM) is crucial for studying gray matter (GM) atrophy in multiple sclerosis (MS).
- Multi-center studies face challenges with cross-scanner variations potentially hindering VBM's effectiveness in detecting disease-specific changes.
- Longitudinal VBM analysis requires understanding inter-site comparability.
Purpose of the Study:
- To evaluate longitudinal inter-site differences and comparability of regional GM in MS patients using VBM.
- To assess the impact of different MRI scanners on detecting GM volume changes over time.
- To determine if data from multiple centers can be pooled for combined analysis.
Main Methods:
- Longitudinal 3D T1-weighted MRI data from 248 relapsing-remitting MS patients across two centers were analyzed.
- Voxel-based morphometry (VBM) was used to assess regional gray matter (GM) volume changes between baseline and year 2.
- Analyses controlled for age, gender, disease duration, and global GM volume, comparing effects between two different 1.5T MR scanners.
Main Results:
- The main effect of time on regional GM volume was larger in center two compared to center one.
- Differential GM volume reductions were observed in fronto-temporal and limbic cortical regions.
- Overall disease-related effects were significant in the cerebellum, uncus, and several cortical/lobular regions, with differential effects being smaller.
Conclusions:
- Scanner-induced effects on longitudinal GM volume differences in MS patients are relatively small.
- The comparability of regional GM changes across different scanners is sufficient.
- Pooling MRI data from multiple centers for combined VBM analysis in MS research is feasible and recommended.

