Xu Jinping, Cheng Qinxiu, Zhang Yue, Luo Yuhan, Zhong Linchang, Liu Huiming, Zhang Haoran, Yang Zhengkun, Zhang Jiana, Ou Zilin, Yan Zhicong, Peng Kangqiang, Liu Gang
Institute of Biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, Guangzhou 510080, China.
Brain Commun. 2025 Jan 20;7(1):fcaf026. doi: 10.1093/braincomms/fcaf026. eCollection 2025.
Although aberrant changes in grey and white matter are core features of idiopathic dystonia, few studies have explored the correlation between grey and white matter changes in this disease. This study aimed to investigate the coupling correlation between morphological and microstructural alterations in patients with idiopathic dystonia. Structural T1 imaging and diffusion tensor imaging were performed on a relatively large cohort of patients. Multidimensional structural analyses, including voxel-based analyses, voxel-based morphology, fixel-based analyses and surface-based morphometry, were performed to explore these structural alterations. Probabilistic tractography and correlation analyses were employed to examine these relationships. A total of 147 patients with idiopathic dystonia and 137 healthy controls were recruited in this study. There were no significant differences in the cortical morphometry between patients with idiopathic dystonia and healthy controls using voxel- and surface-based morphometry. However, the grey matter volume of the bilateral thalamus, fractional anisotropy in the right anterior corona radiata, right retrolenticular part of the internal capsule and right posterior corona radiata, and the fibre density and cross-section combined in the fibre tract connecting the left ventral posterolateral thalamic nucleus and left area 5 m, were significantly decreased in patients with idiopathic dystonia compared with those in healthy controls. Furthermore, the reduced grey matter volume in the right thalamus not only correlated with the disease duration but also with the reduced fractional anisotropy in the right posterior corona radiata and decreased the fibre density and cross-section combined in the fibre tract connecting the left ventral posterolateral thalamic nucleus and the left area 5 m in patients with idiopathic dystonia. These findings suggest that the thalamus is structurally impaired in idiopathic dystonia and that microstructural disruption in thalamocortical projections occurs secondary to thalamic atrophy.
尽管灰质和白质的异常变化是特发性肌张力障碍的核心特征,但很少有研究探讨该疾病中灰质和白质变化之间的相关性。本研究旨在调查特发性肌张力障碍患者形态学和微观结构改变之间的耦合相关性。对相对较大的患者队列进行了结构T1成像和扩散张量成像。进行了多维结构分析,包括基于体素的分析、基于体素的形态学、基于固定点的分析和基于表面的形态测量,以探索这些结构改变。采用概率性纤维束成像和相关性分析来检验这些关系。本研究共招募了147例特发性肌张力障碍患者和137名健康对照。使用基于体素和基于表面的形态测量方法,特发性肌张力障碍患者和健康对照之间的皮质形态测量没有显著差异。然而,与健康对照相比,特发性肌张力障碍患者双侧丘脑的灰质体积、右侧放射冠前部、右侧内囊后肢和右侧放射冠后部的各向异性分数,以及连接左侧丘脑腹后外侧核和左侧5m区的纤维束中的纤维密度和横截面组合均显著降低。此外,右侧丘脑灰质体积的减少不仅与病程相关,还与右侧放射冠后部各向异性分数的降低相关,并降低了特发性肌张力障碍患者连接左侧丘脑腹后外侧核和左侧5m区的纤维束中的纤维密度和横截面组合。这些发现表明,特发性肌张力障碍中丘脑存在结构损伤,丘脑皮质投射的微观结构破坏继发于丘脑萎缩。