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
相关论文
共 36 条
[1]   The clinico-radiological paradox in multiple sclerosis revisited [J].
Barkhof, F .
CURRENT OPINION IN NEUROLOGY, 2002, 15 (03) :239-245
[2]   Imaging outcomes for neuroprotection and repair in multiple sclerosis trials [J].
Barkhof, Frederik ;
Calabresi, Peter A. ;
Miller, David H. ;
Reingold, Stephen C. .
NATURE REVIEWS NEUROLOGY, 2009, 5 (05) :256-266
[3]  
Bendfeldt K, 2011, HUM BRAIN MAP 0429, DOI [10.1002/hbm.21279, DOI 10.1002/HBM.21279.]
[4]   Spatiotemporal Distribution Pattern of White Matter Lesion Volumes and Their Association With Regional Grey Matter Volume Reductions in Relapsing-Remitting Multiple Sclerosis [J].
Bendfeldt, Kerstin ;
Blumhagen, Jan Ole ;
Egger, Hanspeter ;
Loetscher, Patrick ;
Denier, Niklaus ;
Kuster, Pascal ;
Traud, Stefan ;
Mueller-Lenke, Nicole ;
Naegelin, Yvonne ;
Gass, Achim ;
Hirsch, Jochen ;
Kappos, Ludwig ;
Nichols, Thomas E. ;
Radue, Ernst-Wilhelm ;
Borgwardt, Stefan J. .
HUMAN BRAIN MAPPING, 2010, 31 (10) :1542-1555
[5]   Effect of immunomodulatory medication on regional gray matter loss in relapsing-remitting multiple sclerosis-A longitudinal MRI study [J].
Bendfeldt, Kerstin ;
Egger, Hanspeter ;
Nichols, Thomas E. ;
Loetscher, Patrick ;
Denier, Niklaus ;
Kuster, Pascal ;
Traud, Stefan ;
Mueller-Lenke, Nicole ;
Naegelin, Yvonne ;
Gass, Achim ;
Kappos, Ludwig ;
Radue, Ernst-Wilhelm ;
Borgwardt, Stefan J. .
BRAIN RESEARCH, 2010, 1325 :174-182
[6]   Association of regional gray matter volume loss and progression of white matter lesions in multiple sclerosis - A longitudinal voxel-based morphometry study [J].
Bendfeldt, Kerstin ;
Kuster, Pascal ;
Traud, Stefan ;
Egger, Hanspeter ;
Winklhofer, Sebastian ;
Mueller-Lenke, Nicole ;
Naegelin, Yvonne ;
Gass, Achim ;
Kappos, Ludwig ;
Matthews, Paul M. ;
Nichols, Thomas E. ;
Radue, Ernst-Wilhelm ;
Borgwardt, Stefan J. .
NEUROIMAGE, 2009, 45 (01) :60-67
[7]   A voxel-based morphometry study of grey matter loss in MS patients with different clinical phenotypes [J].
Ceccarelli, Antonia ;
Rocca, Maria A. ;
Pagani, Elisabetta ;
Colombo, Bruno ;
Martinelli, Vittorio ;
Comi, Giancarlo ;
Filippi, Massimo .
NEUROIMAGE, 2008, 42 (01) :315-322
[8]   Brain atrophy in clinically early relapsing-remitting multiple sclerosis [J].
Chard, DT ;
Griffin, CM ;
Parker, GJM ;
Kapoor, R ;
Thompson, AJ ;
Miller, DH .
BRAIN, 2002, 125 :327-337
[9]   Statistical mapping analysis of lesion location and neurological disability in multiple sclerosis: application to 452 patient data sets [J].
Charil, A ;
Zijdenbos, AP ;
Taylor, J ;
Boelman, C ;
Worsley, KJ ;
Evans, AC ;
Dagher, A .
NEUROIMAGE, 2003, 19 (03) :532-544
[10]   Brain lesion location and clinical status 20 years after a diagnosis of clinically isolated syndrome suggestive of multiple sclerosis [J].
Dalton, C. M. ;
Bodini, B. ;
Samson, R. S. ;
Battaglini, M. ;
Fisniku, L. K. ;
Thompson, A. J. ;
Ciccarelli, O. ;
Miller, D. H. ;
Chard, D. T. .
MULTIPLE SCLEROSIS JOURNAL, 2012, 18 (03) :322-328