4.3 Article

Gray matter atrophy in relapsing-remitting multiple sclerosis is associated with white matter lesions in connecting fibers

Journal

MULTIPLE SCLEROSIS JOURNAL
Volume 28, Issue 6, Pages 900-909

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/13524585211044957

Keywords

Biomarkers; multiple sclerosis; outcome measurement; relapsing; remitting; T2 lesions; atrophy

Funding

  1. German Research Foundation [DFG SPP2177, 428223038]
  2. National Institutes of Health [1R01NS112161-01]
  3. Macroscale Hub of Munich Cluster for Systems Neurology (SyNergy)

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The study found a close association between brain gray matter atrophy and white matter lesions in connecting fibers in multiple sclerosis patients, indicating a significant correlation between the two. Longitudinal analysis demonstrated a close temporal relation between white matter lesion formation and gray matter atrophy.
Background: Lesions of brain white matter (WM) and atrophy of brain gray matter (GM) are well-established surrogate parameters in multiple sclerosis (MS), but it is unclear how closely these parameters relate to each other. Objective: To assess across the whole cerebrum whether GM atrophy can be explained by lesions in connecting WM tracts. Methods: GM images of 600 patients with relapsing-remitting MS (women = 68%; median age = 33.0 years, median expanded disability status scale score = 1.5) were converted to atrophy maps by data from a healthy control cohort. An atlas of WM tracts from the Human Connectome Project and individual lesion maps were merged to identify potentially disconnected GM regions, leading to individual disconnectome maps. Across the whole cerebrum, GM atrophy and potentially disconnected GM were tested for association both cross-sectionally and longitudinally. Results: We found highly significant correlations between disconnection and atrophy across most of the cerebrum. Longitudinal analysis demonstrated a close temporal relation of WM lesion formation and GM atrophy in connecting fibers. Conclusion: GM atrophy is associated with WM lesions in connecting fibers. Caution is warranted when interpreting group differences in GM atrophy exclusively as differences in early neurodegeneration independent of WM lesion formation.

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