4.3 Article

Spatiotemporal distribution of white matter lesions in relapsing-remitting and secondary progressive multiple sclerosis

期刊

MULTIPLE SCLEROSIS JOURNAL
卷 18, 期 11, 页码 1577-1584

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/1352458512442756

关键词

Multiple sclerosis; MRI; lesion probability maps; white matter; relapsing-remitting; secondary progressive; T1 hypointense lesions; T2 hyperintense lesions

资金

  1. Medical Research Council [G0900908] Funding Source: researchfish
  2. MRC [G0900908] Funding Source: UKRI
  3. Medical Research Council [G0900908] Funding Source: Medline

向作者/读者索取更多资源

Background: Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system. MS lesions show a typical distribution pattern and primarily affect the white matter (WM) in the periventricular zone and in the centrum semiovale. Objective: To track lesion development during disease progression, we compared the spatiotemporal distribution patterns of lesions in relapsing-remitting MS (RRMS) and secondary progressive MS (SPMS). Methods: We used T1 and T2 weighted MR images of 209 RRMS and 62 SPMS patients acquired on two different 1.5 Tesla MR scanners in two clinical centers followed up for 25 (+/- 1.7) months. Both cross-sectional and longitudinal differences in lesion distribution between RRMS and SPMS patients were analyzed with lesion probability maps (LPMs) and permutation-based inference. Results: MS lesions clustered around the lateral ventricles and in the centrum semiovale. Cross-sectionally, compared to RRMS patients, the SPMS patients showed a significantly higher regional probability of T1 hypointense lesions (p <= 0.03) in the callosal body, the corticospinal tract, and other tracts adjacent to the lateral ventricles, but not of T2 lesions (peak probabilities were RRMS: T1 9%, T2 18%; SPMS: T1 21%, T2 27%). No longitudinal changes of regional T1 and T2 lesion volumes between baseline and follow-up scan were found. Conclusion: The results suggest a particular vulnerability to neurodegeneration during disease progression in a number of WM tracts.

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