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孤立性特发性肌张力障碍的影像学见解:基于体素的形态测量学和激活可能性估计研究

Imaging Insights of Isolated Idiopathic Dystonia: Voxel-Based Morphometry and Activation Likelihood Estimation Studies.

作者信息

Wu Yunhao, Zhang Chao, Li Yufei, Feng Jie, Zhang Ming, Li Hongxia, Wang Tao, Zhang Yingying, Jin Zhijia, Zhang Chencheng, Zhang Yuyao, Li Dianyou, Wu Yiwen, Wei Hongjiang, Sun Bomin

机构信息

Department of Neurosurgery, Center for Functional Neurosurgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Front Neurol. 2022 Apr 26;13:823882. doi: 10.3389/fneur.2022.823882. eCollection 2022.

Abstract

The understanding of brain structural abnormalities across different clinical forms of dystonia and their contribution to clinical characteristics remains unclear. The objective of this study is to investigate shared and specific gray matter volume (GMV) abnormalities in various forms of isolated idiopathic dystonia. We collected imaging data from 73 isolated idiopathic dystonia patients and matched them with healthy controls to explore the GMV alterations in patients and their correlations with clinical characteristics using the voxel-based morphometry (VBM) technique. In addition, we conducted an activation likelihood estimation (ALE) meta-analysis of previous VBM studies. Our study demonstrated widespread morphometry alterations in patients with idiopathic dystonia. Multiple systems were affected, which mainly included basal ganglia, sensorimotor, executive control, and visual networks. As the result of the ALE meta-analysis, a convergent cluster with increased GMV was found in the left globus pallidus. In subgroup VBM analyses, decreased putamen GMV was observed in all clinic forms, while the increased GMV was observed in parahippocampal, lingual, and temporal gyrus. GD demonstrated the most extensive GMV abnormalities in cortical regions, and the aberrant GMV of the posterior cerebellar lobe was prominent in CD. Moreover, trends of increased GMV regions of the left precuneus and right superior frontal gyrus were demonstrated in the moderate-outcome group compared with the superior-outcome group. Results of our study indicated shared pathophysiology of the disease-centered on the dysfunction of the basal ganglia-thalamo-cortical circuit, impairing sensorimotor integration, high-level motor execution, and cognition of patients. Dysfunction of the cerebello-thalamo-cortical circuit could also be involved in CD especially. Finally, the frontal-parietal pathway may act as a potential marker for predicting treatment outcomes such as deep brain stimulation.

摘要

对于不同临床类型的肌张力障碍中脑结构异常及其对临床特征的影响,目前仍不清楚。本研究的目的是调查各种形式的孤立性特发性肌张力障碍中共同存在的和特定的灰质体积(GMV)异常。我们收集了73例孤立性特发性肌张力障碍患者的影像数据,并将他们与健康对照进行匹配,采用基于体素的形态学测量(VBM)技术来探索患者的GMV改变及其与临床特征的相关性。此外,我们对先前的VBM研究进行了激活可能性估计(ALE)荟萃分析。我们的研究表明,特发性肌张力障碍患者存在广泛的形态学改变。多个系统受到影响,主要包括基底神经节、感觉运动、执行控制和视觉网络。ALE荟萃分析的结果显示,在左侧苍白球发现一个GMV增加的汇聚簇。在亚组VBM分析中,所有临床类型均观察到壳核GMV减少,而海马旁回、舌回和颞回GMV增加。全身性肌张力障碍(GD)在皮质区域表现出最广泛的GMV异常,而在痉挛性肌张力障碍(CD)中,小脑后叶的GMV异常突出。此外,与良好预后组相比,中等预后组左侧楔前叶和右侧额上回GMV增加区域有上升趋势。我们的研究结果表明,该疾病存在共同的病理生理学——以基底神经节-丘脑-皮质回路功能障碍为中心,损害患者的感觉运动整合、高级运动执行和认知。小脑-丘脑-皮质回路功能障碍尤其可能与CD有关。最后,额顶叶通路可能作为预测深部脑刺激等治疗结果的潜在标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26e0/9087834/004e47158ed7/fneur-13-823882-g0001.jpg

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