A magnetic resonance imaging voxel-based morphometry study of regional gray matter atrophy in patients with benign multiple sclerosis

被引:60
|
作者
Mesaros, Sarlota [1 ]
Rovaris, Marco [1 ,2 ]
Pagani, Elisabetta [1 ]
Pulizzi, Annalisa [2 ]
Caputo, Domenico [3 ,4 ]
Ghezzi, Angelo [5 ]
Bertolotto, Antonio [6 ]
Capra, Ruggero [7 ]
Falautano, Monica [2 ]
Martinelli, Vittorio [2 ]
Comi, Giancarlo [2 ]
Filippi, Massimo [1 ,2 ]
机构
[1] Inst Sci, Neuroimaging Res Unit, I-20132 Milan, Italy
[2] Inst Sci, Dept Neurol, I-20132 Milan, Italy
[3] Univ Osped San Raffaele, San Rafael, CA USA
[4] Sci Inst Don Gnocchi, Dept Neurol, I-20132 Milan, Italy
[5] Osped Gallarate, Multiple Sclerosis Ctr, Gallarate, Italy
[6] Osped Orbassano, Orbassano, Italy
[7] Osped Richiedei, Gussago, Italy
关键词
D O I
10.1001/archneur.65.9.1223
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Evidence is accumulating that indicates that a selected assessment of gray matter (GM) damage is able to provide strong paraclinical correlates of multiple sclerosis (MS) severity. Objective: To investigate the pattern of regional GM atrophy in patients with benign MS (BMS) vs those with secondary progressive MS (SPMS) to better elucidate the factors associated with a favorable status in patients with MS. Design: Cross-sectional survey from January 2006 to August 2007. Setting: Referral, hospital-based MS clinics. Patients: Sixty patients with BMS, 35 patients with SPMS, and 21 healthy volunteers. Main Outcome Measures: Neuropsychological tests exploring memory, attention, and frontal lobe cognitive domains were administered to BMS patients. A voxel-based morphometry analysis of GM concentration was performed using statistical parametric mapping and a threshold of 0.05, corrected for multiple comparisons. Results: Twelve BMS patients(20%) hadan abnormal performance on 3 or more neuropsychological tests. Compared with healthy individuals, BMS patients had a reduced GM volume in the subcortical and frontoparietal regions. Compared with BMS patients, those with SPMS had a significant GM loss in the cerebellum. No differences between BMS and SPMS patients were found when only BMS patients with cognitive impairment or those with shorter disease duration (15-19 years) and higher Expanded Disability Status Scale scores (>2.0) were considered. Conclusions: Cerebellar GM atrophy seems to be a major determinant of irreversible locomotor disability in MS. The absence of cognitive impairment and a longer disease duration or lower Expanded Disability Status Scale score may identify those BMS patients with the potential for a favorable disease evolution.
引用
收藏
页码:1223 / 1230
页数:8
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