Louapre Céline, Govindarajan Sindhuja T, Giannì Costanza, Madigan Nancy, Nielsen A Scott, Sloane Jacob A, Kinkel Revere P, Mainero Caterina
A. A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, USA; Harvard Medical School, Boston, MA, USA.
A. A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, USA.
Neuroimage Clin. 2016 Nov 3;12:879-886. doi: 10.1016/j.nicl.2016.11.001. eCollection 2016.
Using quantitative T* at 7 Tesla (T) magnetic resonance imaging, we investigated whether impairment in selective cognitive functions in multiple sclerosis (MS) can be explained by pathology in specific areas and/or layers of the cortex. Thirty-one MS patients underwent neuropsychological evaluation, acquisition of 7 T multi-echo T* gradient-echo sequences, and 3 T anatomical images for cortical surfaces reconstruction. Seventeen age-matched healthy subjects served as controls. Cortical T* maps were sampled at various depths throughout the cortex and juxtacortex. Relation between T*, neuropsychological scores and a cognitive index (CI), calculated from a principal component analysis on the whole battery, was tested by a general linear model. Cognitive impairment correlated with T* increase, independently from white matter lesions and cortical thickness, in cortical areas highly relevant for cognition belonging to the default-mode network (p < 0.05 corrected). Dysfunction in different cognitive functions correlated with longer T* in selective cortical regions, most of which showed longer T* relative to controls. For most tests, this association was strongest in deeper cortical layers. Executive dysfunction, however, was mainly related with pathology in juxtameningeal cortex. T* explained up to 20% of the variance of the CI, independently of conventional imaging metrics (adjusted-R: 52-67%, p < 5.10). Location of pathology across the cortical width and mantle showed selective correlation with impairment in differing cognitive domains. These findings may guide studies at lower field strength designed to develop surrogate markers of cognitive impairment in MS.
利用7特斯拉(T)磁共振成像中的定量T*,我们研究了多发性硬化症(MS)中选择性认知功能障碍是否可由皮质特定区域和/或层的病理学来解释。31例MS患者接受了神经心理学评估、7T多回波T梯度回波序列采集以及用于皮质表面重建的3T解剖图像采集。17名年龄匹配的健康受试者作为对照。在整个皮质和皮质旁的不同深度对皮质T图进行采样。通过一般线性模型测试T*、神经心理学评分与认知指数(CI)之间的关系,该认知指数是通过对整个测试组进行主成分分析计算得出的。认知障碍与属于默认模式网络的、与认知高度相关的皮质区域中T的增加相关,与白质病变和皮质厚度无关(校正后p<0.05)。不同认知功能的功能障碍与选择性皮质区域中较长的T相关,其中大多数区域相对于对照组显示出较长的T*。对于大多数测试,这种关联在皮质较深层最为明显。然而,执行功能障碍主要与软脑膜旁皮质的病理学有关。T*可解释CI变异的20%,独立于传统成像指标(调整R:52 - 67%,p<5.10)。皮质宽度和皮质层中病理学的位置与不同认知领域的损伤存在选择性相关性。这些发现可能会指导在较低场强下开展的研究,旨在开发MS认知障碍的替代标志物。