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Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
White and gray matter damage in primary progressive MS: The chicken or the egg?
Benedetta Bodini1, Declan Chard2, Daniel R Altmann2
1From the Department of Neuroinflammation (B.B., D.C., D.R.A., D.T., D.H.M., A.J.T., C.W.-K., O.C.), Queen Square MS Centre, University College of London Institute of Neurology; Department of Neuroimaging (B.B.), Institute of Psychiatry, King's College London; London School of Hygiene and Tropical Medicine (D.R.A.), University of London; NIHR UCL/UCLH Biomedical Research Centre (D.H.M., A.J.T., O.C.), London, UK. benedetta.bodini@icm-institute.org.
Objective:
The temporal relationship between white matter (WM) and gray matter (GM) damage in vivo in early primary progressive multiple sclerosis (PPMS) was investigated testing 2 hypotheses: (1) WM tract abnormalities predict subsequent changes in the connected cortex ("primary WM damage model"); and (2) cortical abnormalities predict later changes in connected WM tracts ("primary GM damage model").
Methods:
Forty-seven patients with early PPMS and 18 healthy controls had conventional and magnetization transfer imaging at baseline; a subgroup of 35 patients repeated the protocol after 2 years. Masks of the corticospinal tracts, genu of the corpus callosum and optic radiations, and of connected cortical regions, were used for extracting the mean magnetization transfer ratio (MTR). Multiple regressions within each of 5 tract-cortex pairs were performed, adjusting for the dependent variable's baseline MTR; tract lesion load and MTR, spinal cord area, age, and sex were examined for potential confounding.
Results:
The baseline MTR of most regions was lower in patients than in healthy controls. The tract-cortex pair relationships in the primary WM damage model were significant for the bilateral motor pair and right visual pair, while those in the primary GM damage model were only significant for the right motor pair. Lower lesion MTR at baseline was associated with lower MTR in the same tract normal-appearing WM at 2 years in 3 tracts.
Conclusion:
These results are consistent with the hypothesis that in early PPMS, cortical damage is for the most part a sequela of normal-appearing WM pathology, which, in turn, is predicted by abnormalities within WM lesions.
Insights
In early primary progressive multiple sclerosis (PPMS), white matter (WM) lesions predict gray matter (GM) damage. This suggests WM pathology drives cortical changes in PPMS.
Area of Science:
- Neuroimaging
- Neurology
- Multiple Sclerosis Research
Background:
- Primary progressive multiple sclerosis (PPMS) is characterized by progressive neurological decline.
- Understanding the temporal relationship between white matter (WM) and gray matter (GM) damage is crucial for PPMS progression.
- Existing models propose either primary WM or GM damage initiating the disease cascade.
Purpose of the Study:
- To investigate the temporal sequence of WM and GM damage in vivo in early PPMS.
- To test the hypothesis that WM tract abnormalities precede cortical changes.
- To test the hypothesis that cortical abnormalities precede WM tract changes.
Main Methods:
- Magnetization transfer imaging (MTI) was used to assess WM and GM integrity in 47 early PPMS patients and 18 controls.
- Imaging was performed at baseline and after 2 years in a subgroup of patients.
- Tract-based and region-of-interest analyses were conducted to evaluate relationships between WM and GM damage.
Main Results:
- Patients with PPMS showed lower MTR values in most regions compared to controls.
- WM damage significantly predicted subsequent GM damage in motor and visual pathways.
- Normal-appearing WM MTR at 2 years was associated with baseline lesion MTR in affected tracts.
Conclusions:
- Findings support a primary WM damage model in early PPMS.
- Cortical damage appears to be a consequence of underlying WM pathology.
- Abnormalities within WM lesions are predictive of subsequent normal-appearing WM changes and downstream cortical damage.
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