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

被引:19
作者
Filli, Lukas [1 ]
Hofstetter, Louis [1 ]
Kuster, Pascal [1 ]
Traud, Stefan [1 ]
Mueller-Lenke, Nicole [1 ]
Naegelin, Yvonne [2 ]
Kappos, Ludwig [2 ]
Gass, Achim [2 ]
Sprenger, Till [2 ]
Nichols, Thomas E. [3 ,4 ]
Vrenken, Hugo
Barkhof, Frederik
Polman, Chris
Radue, Ernst-Wilhelm [1 ]
Borgwardt, Stefan J. [1 ]
Bendfeldt, Kerstin [1 ]
机构
[1] Univ Basel Hosp, Med Image Anal Ctr, CH-4031 Basel, Switzerland
[2] Univ Basel Hosp, Dept Neurol, CH-4031 Basel, Switzerland
[3] Univ Warwick, Dept Stat, Coventry CV4 7AL, W Midlands, England
[4] Univ Warwick, Warwick Mfg Grp, Coventry CV4 7AL, W Midlands, England
基金
英国医学研究理事会;
关键词
Multiple sclerosis; MRI; lesion probability maps; white matter; relapsing-remitting; secondary progressive; T1 hypointense lesions; T2 hyperintense lesions; VOXEL-BASED MORPHOMETRY; MEMORY PERFORMANCE; ATROPHY; BRAIN; MRI; HYPERINTENSITIES; ASSOCIATION; IMPAIRMENT; DISABILITY; DIAGNOSIS;
D O I
10.1177/1352458512442756
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:1577 / 1584
页数:8
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