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Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
Published on: July 28, 2013
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Gray matter integrity predicts white matter network reorganization in multiple sclerosis
Angela Radetz1, Nabin Koirala1, Julia Krämer2
1Department of Neurology and Neuroimaging Center (NIC) of the Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Human Brain Mapping
|February 7, 2020
Summary
In multiple sclerosis (MS), deep gray matter atrophy drives white matter network changes, not the other way around. Deep gray matter volume predicts future disability and cognitive decline in MS patients.
Area of Science:
- Neuroscience
- Radiology
- Neurology
Background:
- Multiple sclerosis (MS) is a chronic inflammatory and neurodegenerative disease.
- MS leads to gray matter atrophy and brain network reconfiguration.
- The relationship between white matter and gray matter changes in MS is not fully understood.
Purpose of the Study:
- To investigate whether white matter network reconfiguration follows gray matter damage or vice versa in early MS.
- To assess the predictive value of gray matter integrity for clinical outcomes.
Main Methods:
- MRI data from 83 patients with early MS were analyzed over a 1-year follow-up.
- White matter network integrity was assessed using graph theoretical analyses of diffusion-weighted data.
- Gray matter integrity was evaluated by measuring cortical thickness and deep gray matter volume.
Main Results:
- Significant atrophy was observed in the middle temporal cortex, thalamus, caudate, putamen, and brain stem.
- Deep gray matter volume changes predicted white matter network dynamics (modularity and distance measures).
- Initial white matter properties did not predict atrophy; however, baseline gray matter integrity predicted physical disability and cognitive performance.
Conclusions:
- Deep gray matter atrophy appears to drive white matter network adaptations in MS.
- Deep gray matter volume is a strong predictor of disability progression and cognitive impairment in early MS.

