Kamagata Koji, Zalesky Andrew, Hatano Taku, Ueda Ryo, Di Biase Maria Angelique, Okuzumi Ayami, Shimoji Keigo, Hori Masaaki, Caeyenberghs Karen, Pantelis Christos, Hattori Nobutaka, Aoki Shigeki
Department of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Melbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne & Melbourne Health, Parkville, VIC, Australia.
Hum Brain Mapp. 2017 Jul;38(7):3704-3722. doi: 10.1002/hbm.23628. Epub 2017 May 4.
Mapping gray matter (GM) pathology in Parkinson's disease (PD) with conventional MRI is challenging, and the need for more sensitive brain imaging techniques is essential to facilitate early diagnosis and assessment of disease severity. GM microstructure was assessed with GM-based spatial statistics applied to diffusion kurtosis imaging (DKI) and neurite orientation dispersion imaging (NODDI) in 30 participants with PD and 28 age- and gender-matched controls. These were compared with currently used assessment methods such as diffusion tensor imaging (DTI), voxel-based morphometry (VBM), and surface-based cortical thickness analysis. Linear discriminant analysis (LDA) was also used to test whether subject diagnosis could be predicted based on a linear combination of regional diffusion metrics. Significant differences in GM microstructure were observed in the striatum and the frontal, temporal, limbic, and paralimbic areas in PD patients using DKI and NODDI. Significant correlations between motor deficits and GM microstructure were also noted in these areas. Traditional VBM and surface-based cortical thickness analyses failed to detect any GM differences. LDA indicated that mean kurtosis (MK) and intra cellular volume fraction (ICVF) were the most accurate predictors of diagnostic status. In conclusion, DKI and NODDI can detect cerebral GM abnormalities in PD in a more sensitive manner when compared with conventional methods. Hence, these methods may be useful for the diagnosis of PD and assessment of motor deficits. Hum Brain Mapp 38:3704-3722, 2017. © 2017 Wiley Periodicals, Inc.
利用传统磁共振成像(MRI)描绘帕金森病(PD)中的灰质(GM)病理学具有挑战性,因此需要更敏感的脑成像技术来促进疾病的早期诊断和严重程度评估。在30名帕金森病患者和28名年龄及性别匹配的对照者中,应用基于GM的空间统计学方法对扩散峰度成像(DKI)和神经突方向离散成像(NODDI)的GM微观结构进行评估。将这些结果与目前使用的评估方法进行比较,如扩散张量成像(DTI)、基于体素的形态学测量(VBM)和基于表面的皮质厚度分析。还使用线性判别分析(LDA)来测试是否可以基于区域扩散指标的线性组合预测受试者的诊断。使用DKI和NODDI观察到帕金森病患者的纹状体以及额叶、颞叶、边缘叶和边缘旁区域的GM微观结构存在显著差异。在这些区域还发现运动功能障碍与GM微观结构之间存在显著相关性。传统的VBM和基于表面的皮质厚度分析未能检测到任何GM差异。LDA表明,平均峰度(MK)和细胞内体积分数(ICVF)是诊断状态最准确的预测指标。总之,与传统方法相比,DKI和NODDI能够更敏感地检测帕金森病中的脑GM异常。因此,这些方法可能有助于帕金森病的诊断和运动功能障碍的评估。《人类大脑图谱》38:3704 - 3722, 2017。© 2017威利期刊公司。