帕金森病的脑灰质体积改变的VBM研究

目的 分析帕金森病(PD)患者的全脑灰质体积的变化,探讨PD患者的脑灰质结构异常模式.方法 选取符合入组标准的46例PD患者和19例年龄、性别与之相匹配的正常对照(NC)被试者作为研究对象.46例PD患者按改良的Hoehn-Yahr (H-Y)分级标准又分为2个亚组,25例早期PD(ePD)组和21例中晚期PD(maPD)组.所有受试者在3.0T超高场磁共振仪进行常规磁共振扫描,并获取三维高分辨T1WI数据,采用VBM-DARTEL(voxel-based morphometry-diffeomorphic anatomical registration through exponentiated lie)方法分析比较PD组与NC组、ePD组与maPD组间的脑灰质体积差异.结果 与NC组相比,PD组双侧额叶、颞叶、岛叶、扣带回、海马、梭状回、小脑及右侧楔叶、楔前叶等脑区的灰质体积减小,全脑灰质未见体积增加.与ePD组相比,maPD组双侧额叶、颞叶、岛叶、扣带回、直回、舌回、梭状回、海马、杏仁核及小脑等脑区的灰质体积减小.结论 VBM方法客观提示了PD存在广泛的脑灰质萎缩,且随病程的进展更为显著.PD脑结构的变化存在特定的空间分布模式,可能与PD的病理基础有关.

Changes of the brain gray matter in Parkinson's disease:a voxel-based morphometry study

Objective To analyze and evaluate changes of the brain gray matter in patients with Parkinson's disease (PD).Methods 46 patients with PD and 19 normal control(NC) subjects(matched to the patients in age and gender) were selected in this study.46 cases of PD were divided into early PD group(ePD,25 cases) and middle-advanced PD group(maPD,21 cases) by improved Hoehn-Yahr(H-Y) stages.All the subjects underwent 3.0T MR scanning,and data of high resolution T1-weighted imageing (T1WI) were acquired.Gray matter volume differences between PD group and NC group,or ePD group and maPD group were assessed by voxel-based morphometry (VBM) combined diffeomorphic anatomical registration through exponentiated lie (DARTEL) method.Results The gray matter volume of the bilateral frontal lobes, temporal lobes, insular lobes, cingulum gyrus, hippocampus, fusiform gyrus, cerebellum and right cuneus lobe and precuneus lobe in the PD group was smaller than that in the NC group.The gray matter volume of the bilateral frontal lobes, temporal lobes,insular lobes,cingulum gyrus,rectus gyrus,lingualis gyrus,fusiform gyrus,hippocampus,amygdaloid and cerebellum in the maPD group was smaller than that in the ePD group.Conclusion VBM reveals a widespread volume reduction of the gray matter in PD patients,and detectes a correlation with disease duration and severity.These changes located in special distribution may be in line with the pathology of PD.