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威尔逊病中运动执行网络拓扑组织的破坏

Disrupted topological organization of the motor execution network in Wilson's disease.

作者信息

Zhu Long, Yin Hongxi, Wang Yanxin, Yang Wenming, Dong Ting, Xu Lei, Hou Zhifeng, Shi Qiao, Shen Qi, Lin Zicheng, Zhao Haixia, Xu Yaqin, Chen Yanyan, Wu Jingjing, Yu Zheng, Wen Man, Huang Jiaying

机构信息

Department of Encephalopathy, The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hefei, China.

出版信息

Front Neurol. 2022 Nov 21;13:1029669. doi: 10.3389/fneur.2022.1029669. eCollection 2022.

DOI:10.3389/fneur.2022.1029669
PMID:36479050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9721349/
Abstract

OBJECTIVE

There are a number of symptoms associated with Wilson's disease (WD), including motor function damage. The neuropathological mechanisms underlying motor impairments in WD are, however, little understood. In this study, we explored changes in the motor execution network topology in WD.

METHODS

We conducted resting-state functional magnetic resonance imaging (fMRI) on 38 right-handed individuals, including 23 WD patients and 15 healthy controls of the same age. Based on graph theory, a motor execution network was constructed and analyzed. In this study, global, nodal, and edge topological properties of motor execution networks were compared.

RESULTS

The global topological organization of the motor execution network in the two groups did not differ significantly across groups. In the cerebellum, WD patients had a higher nodal degree. At the edge level, a cerebello-thalamo-striato-cortical circuit with altered functional connectivity strength in WD patients was observed. Specifically, the strength of the functional connections between the cerebellum and thalamus increased, whereas the cortical-thalamic, cortical-striatum and cortical-cerebellar connections exhibited a decrease in the strength of the functional connection.

CONCLUSION

There is a disruption of the topology of the motor execution network in WD patients, which may be the potential basis for WD motor dysfunction and may provide important insights into neurobiological research related to WD motor dysfunction.

摘要

目的

威尔逊病(WD)存在多种症状,包括运动功能损害。然而,WD运动障碍背后的神经病理机制尚不清楚。在本研究中,我们探讨了WD患者运动执行网络拓扑结构的变化。

方法

我们对38名右利手个体进行了静息态功能磁共振成像(fMRI),其中包括23名WD患者和15名年龄匹配的健康对照者。基于图论构建并分析运动执行网络。在本研究中,比较了运动执行网络的全局、节点和边的拓扑属性。

结果

两组运动执行网络的全局拓扑组织在组间无显著差异。在小脑中,WD患者的节点度更高。在边的层面,观察到WD患者中一个功能连接强度改变的小脑-丘脑-纹状体-皮质回路。具体而言,小脑与丘脑之间的功能连接强度增加,而皮质-丘脑、皮质-纹状体和皮质-小脑连接的功能连接强度降低。

结论

WD患者运动执行网络的拓扑结构存在破坏,这可能是WD运动功能障碍的潜在基础,并可能为与WD运动功能障碍相关的神经生物学研究提供重要见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/cd014ceddc1e/fneur-13-1029669-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/8281ebe4cc50/fneur-13-1029669-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/4b8c669db9aa/fneur-13-1029669-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/97e0da7e79d1/fneur-13-1029669-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/cd014ceddc1e/fneur-13-1029669-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/8281ebe4cc50/fneur-13-1029669-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/4b8c669db9aa/fneur-13-1029669-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/97e0da7e79d1/fneur-13-1029669-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4c/9721349/cd014ceddc1e/fneur-13-1029669-g0004.jpg

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