Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Department of Neurology, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Hum Brain Mapp. 2017 Nov;38(11):5648-5665. doi: 10.1002/hbm.23755. Epub 2017 Aug 9.
In this longitudinal study, we investigated the regional patterns of focal lesions accumulation, and gray (GM) and white matter (WM) atrophy progression over a five-year follow-up (FU) in multiple sclerosis (MS) patients and their association with clinical and cognitive deterioration. Neurological, neuropsychological and brain MRI (dual-echo and 3D T1-weighted sequences) assessments were prospectively performed at baseline (T0) and after a median FU of 4.9 years from 66 MS patients (including relapse-onset and primary progressive MS) and 16 matched controls. Lesion probability maps were obtained. Longitudinal changes of GM and WM volumes and their association with clinical and cognitive deterioration were assessed using tensor-based morphometry and SPM12. At FU, 36/66 (54.5%) MS patients showed a significant disability worsening, 14/66 (21.2%) evolved to a worse clinical phenotype, and 18/63 (28.6%) developed cognitive deterioration. At T0, compared to controls, MS patients showed a widespread pattern of GM atrophy, involving cortex, deep GM and cerebellum, and atrophy of the majority of WM tracts, which further progressed at FU (P < 0.001, uncorrected). Compared to stable patients, those with clinical and cognitive worsening showed a left-lateralized pattern of GM and WM atrophy, involving deep GM, fronto-temporo-parieto-occipital regions, cerebellum, and several WM tracts (P < 0.001, uncorrected).GM and WM atrophy of relevant brain regions occur in MS after 5 years. A different vulnerability of the two brain hemispheres to irreversible structural damage may be among the factors contributing to clinical and cognitive worsening in these patients. Hum Brain Mapp 38:5648-5665, 2017. © 2017 Wiley Periodicals, Inc.
在这项纵向研究中,我们研究了多发性硬化症 (MS) 患者在五年随访 (FU) 期间焦点病变积累的区域模式,以及灰质 (GM) 和白质 (WM) 萎缩的进展情况,及其与临床和认知恶化的关系。在基线 (T0) 时,前瞻性地对 66 名 MS 患者 (包括复发型和原发性进展型 MS) 和 16 名匹配的对照组进行了神经学、神经心理学和脑 MRI(双回波和 3D T1 加权序列)评估,随访中位数为 4.9 年。获得了病变概率图。使用基于张量的形态测量法和 SPM12 评估 GM 和 WM 体积的纵向变化及其与临床和认知恶化的关系。在 FU 时,66 名 MS 患者中有 36 名 (54.5%) 出现明显的残疾恶化,14 名 (21.2%) 发展为更差的临床表型,18 名 (28.6%) 出现认知恶化。在 T0 时,与对照组相比,MS 患者的 GM 萎缩广泛,包括皮质、深部 GM 和小脑,以及大多数 WM 束的萎缩,在 FU 时进一步进展 (P < 0.001,未校正)。与稳定的患者相比,那些出现临床和认知恶化的患者出现了 GM 和 WM 萎缩的左侧偏侧化模式,涉及深部 GM、额颞顶枕叶区域、小脑和几个 WM 束 (P < 0.001,未校正)。在 MS 患者中,5 年后 GM 和 WM 萎缩发生。两个大脑半球对不可逆结构损伤的不同易损性可能是导致这些患者临床和认知恶化的因素之一。人脑映射 38:5648-5665, 2017. Wiley Periodicals, Inc.