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Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Regional brain atrophy in children with multiple sclerosis
B Aubert-Broche1, V Fonov, R Ghassemi
1McConnell Brain Imaging Center, Montreal Neurological Institute, McGill University, Montreal, Canada.
Insights
Pediatric multiple sclerosis (MS) patients show reduced brain volume, particularly in the thalamus and corpus callosum. Lesions correlate with splenium volume loss, while optic pathway degeneration links to disease duration.
Area of Science:
- Neuroimaging
- Pediatric Neurology
- Multiple Sclerosis Research
Background:
- Pediatric multiple sclerosis (MS) involves complex neuroinflammatory processes affecting brain structure.
- Accurate volumetric assessment in children requires accounting for age- and sex-related brain development.
Purpose of the Study:
- To quantify regional brain volume differences in pediatric MS patients compared to healthy controls.
- To investigate the relationship between lesion load, disease duration, and specific brain volume changes.
Main Methods:
- Cross-sectional tensor-based morphometry (TBM) was employed.
- Jacobian determinant normalized for age and sex was used to measure local volume differences.
- Voxel-wise analysis compared pediatric MS patients to age- and sex-matched controls.
Main Results:
- Pediatric MS patients exhibited reduced volumes in the thalamus and splenium of the corpus callosum, alongside ventricular expansion.
- T2-weighted lesion volume correlated with reduced splenium volume but not thalamic volume.
- Optic pathway volumes (tracts and radiations) showed reduced volume correlated with disease duration.
Conclusions:
- Brain volume reduction in specific regions is evident in pediatric MS.
- Focal inflammatory lesions may contribute to degeneration in white matter tracts.
- Optic pathway degeneration is associated with disease duration, suggesting transsynaptic effects.
Abstract:
We used cross-sectional tensor-based morphometry to visualize reduced volume in the whole brains of pediatric patients with multiple sclerosis, relative to healthy controls. As a marker of local volume difference, we used the Jacobian determinant of the deformation field that maps each subject to a standard space. To properly assess abnormal differences in volume in this age group, it is necessary to account for the normal, age-related differences in brain volume. This was accomplished by computing normalized z-score Jacobian determinant values at each voxel to represent the local volume difference (in standard deviations) between an individual subject and an age- and sex-matched healthy normal population. Compared with healthy controls, pediatric patients with multiple sclerosis exhibited significantly reduced volumes within the thalamus and the splenium of the corpus callosum and significant expansions in the ventricles. While T2-weighted lesion volume was correlated with reduced splenium volume, no correlation was found between T2-weighted lesion volume and reduced thalamic volume. Reduced volumes of the optic pathways, including that of the optic tracts and optic radiations, correlated with disease duration. Our results suggest that focal inflammatory lesions may play an important role in tract degeneration, including transsynaptic degeneration.
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