Wang Dongcui, Jin Hong, Xie Fangfang, Wang Ziyun, Xing Wu
Department of Radiology, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, XiangYa Hospital, Central South University, Changsha, China.
Heliyon. 2024 Aug 22;10(17):e36739. doi: 10.1016/j.heliyon.2024.e36739. eCollection 2024 Sep 15.
Previous studies have indicated that patients with Paroxysmal Kinesigenic Dyskinesia (PKD) exhibit reduced gray matter volume in certain brain regions within the cortico-striato-thalamo-cortical (CSTC) loop. However, a comprehensive investigation specifically targeting the CSTC loop in PKD has never been conducted.
To provide evidence for the involvement of the CSTC loop in the pathogenesis of PKD from the perspective of structural alterations, this study carried out a surface-based morphometry (SBM), voxel-based morphometry (VBM), and structural covariance networks (SCN) combined analysis in familial PKD patients.
A total of 8 familial PKD patients and 10 healthy family members were included in the study and underwent Brain MRI examinations. Based on 3D T1 MPRAGE data, neuroimaging metrics of cortical thickness from SBM, subcortical nuclei volume from VBM, and covariance coefficient from SCN were used to systematically investigate the brain structural alterations along the CSTC loop of PKD patients.
A significant decrease in the average cortical thickness of the left S1 region in the PKD group was observed. The volumes of subcortical nuclei, including the thalamus, putamen, and globus pallidus were reduced, with a pronounced effect observed in the bilateral putamen. And the structural covariance connection between the left putamen and the left globus pallidus was significantly strengthened.
The study confirms the involvement of the CSTC loop in the pathogenesis of PKD from the perspective of structural alterations, and the findings may provide potential targets for objective diagnosis and therapeutic monitoring of PKD.
既往研究表明,发作性运动诱发性运动障碍(PKD)患者在皮质-纹状体-丘脑-皮质(CSTC)环路的某些脑区灰质体积减少。然而,从未针对PKD中的CSTC环路进行过全面研究。
为了从结构改变的角度提供CSTC环路参与PKD发病机制的证据,本研究对家族性PKD患者进行了基于表面的形态学测量(SBM)、基于体素的形态学测量(VBM)和结构协方差网络(SCN)联合分析。
本研究共纳入8例家族性PKD患者和10名健康家庭成员,并进行了脑部MRI检查。基于三维T1加权磁化准备快速梯度回波(MPRAGE)数据,使用SBM的皮质厚度、VBM的皮质下核体积和SCN的协方差系数等神经影像学指标,系统研究PKD患者CSTC环路的脑结构改变。
PKD组左侧初级体感区(S1)平均皮质厚度显著降低。包括丘脑、壳核和苍白球在内的皮质下核体积减小,双侧壳核受影响明显。并且左侧壳核与左侧苍白球之间的结构协方差连接显著增强。
本研究从结构改变的角度证实了CSTC环路参与PKD的发病机制,研究结果可能为PKD的客观诊断和治疗监测提供潜在靶点。