胼胝体
医学
白质
部分各向异性
脾
磁共振弥散成像
光辐射
磁共振成像
上纵束
穹窿
神经科学
解剖
心理学
内科学
放射科
海马体
作者
Lorenzo Conti,Paolo Preziosa,Alessandro Meani,Elisabetta Pagani,Paola Valsasina,Olga Marchesi,Carmen Vizzino,Maria A. Rocca,Massimo Filippi
摘要
Abstract Background Cognitive impairment frequently affects multiple sclerosis (MS) patients. However, its neuroanatomical correlates still need to be fully explored. We investigated the contribution of structural and functional magnetic resonance imaging (MRI) abnormalities in explaining cognitive impairment in MS. Methods Brain dual‐echo, diffusion tensor, 3D T1‐weighted and resting‐state (RS) MRI sequences were acquired from 276 MS patients and 102 healthy controls. Using random forest analysis, the contribution of regional white matter (WM) lesions, WM fractional anisotropy (FA) abnormalities, gray matter (GM) atrophy and RS functional connectivity (FC) alterations to cognitive impairment in MS patients was investigated. Results Eighty‐four MS patients (30.4%) were cognitively impaired. The best MRI predictors of cognitive impairment (relative importance [%]) (out‐of‐bag area under the curve [AUC] = 0.795) were (a) WM lesions in the right superior longitudinal fasciculus (100%), left anterior thalamic radiation (93.4%), left posterior corona radiata (78.5%), left medial lemniscus (74.2%), left inferior longitudinal fasciculus (70.4%), left optic radiation (68.7%), right middle cerebellar peduncle (60.6%) and right optic radiation (53.5%); (b) decreased FA in the splenium of the corpus callosum (64.3%), left optic radiation (61.0%), body of the corpus callosum (51.9%) and fornix (50.9%); and (c) atrophy of the left precuneus (91.4%), right cerebellum crus I (84.4%), right caudate nucleus (78.6%), left thalamus (76.2%) and left supplementary motor area (59.8%). The relevance of these MRI measures in explaining cognitive impairment was confirmed in a cross‐validation analysis (AUC =0.765). Conclusion Structural damage in strategic WM and GM regions explains cognitive impairment in MS patients more than RS FC abnormalities.
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