Chen J T, Narayanan S, Collins D L, Smith S M, Matthews P M, Arnold D L
Montreal Neurological Institute and Hospital, McConnell Brain Imaging Centre, 3801 University, WB 321, Montreal, Quebec, Canada H3A 2B4.
Neuroimage. 2004 Nov;23(3):1168-75. doi: 10.1016/j.neuroimage.2004.07.046.
Cortical grey matter (cGM) develops a substantial burden of pathology in multiple sclerosis (MS). Previous cross-sectional studies have suggested a relationship between measures of cortical atrophy and disability. Our objective was to develop a method for automatically measuring the apparent cGM thickness as well as the integrity of the interface between cGM and subcortical white matter (GM/WM) both globally and regionally on T(1)-weighted MRI, and use this method in a longitudinal investigation of how these measures differed between patients with stable MS and patients with progressing disability. Measurements were made over the whole brain and for anatomically specified cortical regions, both cross-sectionally at baseline and longitudinally on two MRI scans performed on average 1 year apart. We found a higher average rate of apparent loss of cGM thickness across the whole brain in the group that progressed over the interscan interval compared to the group that remained stable (progressing = -3.13 +/- 2.88%/year, stable = 0.06 +/- 2.31%/year, P = 0.002). This difference was detected with regional measures in parietal and precentral cortex. In contrast, change in the GM/WM interface integrity did not show detectable regional differences, although the group of MS patients whose disability progressed showed a significant decrease in GM/WM interface integrity compared to the stable group (P = 0.003). Regional measures of apparent loss of cGM thickness enhance sensitivity to cortical pathological changes. A measure of integrity offers a new index of disease-associated cortical changes at the GM/WM interface. The results suggest that progression of disability in MS is associated with the progression of MRI-detectable cortical pathology.
皮质灰质(cGM)在多发性硬化症(MS)中会出现大量病理负担。以往的横断面研究表明皮质萎缩测量值与残疾之间存在关联。我们的目标是开发一种方法,用于在T(1)加权磁共振成像(MRI)上自动测量全脑及局部的cGM表观厚度以及cGM与皮质下白质(GM/WM)之间界面的完整性,并在一项纵向研究中使用该方法,以探究这些测量值在病情稳定的MS患者和残疾进展患者之间有何差异。在基线时进行横断面测量,并在平均相隔1年进行的两次MRI扫描上进行纵向测量,测量范围涵盖全脑以及解剖学上特定的皮质区域。我们发现,与病情保持稳定的组相比,在两次扫描间隔期内病情进展的组全脑cGM厚度表观损失的平均速率更高(进展组 = -3.13 +/- 2.88%/年,稳定组 = 0.06 +/- 2.31%/年,P = 0.002)。在顶叶和中央前回皮质的局部测量中也检测到了这种差异。相比之下,GM/WM界面完整性的变化未显示出可检测到的局部差异,尽管与稳定组相比,残疾进展的MS患者组GM/WM界面完整性显著降低(P = 0.003)。cGM厚度表观损失的局部测量提高了对皮质病理变化的敏感性。界面完整性测量提供了一个与疾病相关的GM/WM界面皮质变化的新指标。结果表明,MS中残疾的进展与MRI可检测到的皮质病理进展相关。