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多发性硬化症患者纹状体亚区功能连接的改变

Altered Functional Connectivity of Striatal Subregions in Patients with Multiple Sclerosis.

作者信息

Cui Fangyuan, Zhou Li, Wang Zengjian, Lang Courtney, Park Joel, Tan Zhongjian, Yu Yao, Sun Chunyan, Gao Ying, Kong Jian

机构信息

Department of Neurology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.

Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA.

出版信息

Front Neurol. 2017 Apr 24;8:129. doi: 10.3389/fneur.2017.00129. eCollection 2017.

DOI:10.3389/fneur.2017.00129
PMID:28484419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5401875/
Abstract

Abnormal corticostriatal resting-state functional connectivity (rsFC) has been implicated in the neuropathology of multiple sclerosis. The striatum, a component of the basal ganglia, is involved in diverse functions including movement, cognition, emotion, and limbic information processing. However, the brain circuits of the striatal subregions contributing to the changes in rsFC in relapsing-remitting multiple sclerosis (RRMS) patients remain unknown. We used six subdivisions of the striatum in each hemisphere as seeds to investigate the rsFC of striatal subregions between RRMS patients and matched healthy controls (HCs). In addition, we also scanned a subcohort of RRMS patients after an average of 7 months to test the reliability of our findings. Compared to HCs, we found significantly increased dorsal caudal putamen (DCP) connectivity with the premotor area, dorsal lateral prefrontal cortex (DLPFC), insula, precuneus, and superior parietal lobule, and significantly increased connectivity between the superior ventral striatum and posterior cingulate cortex (PCC) in RRMS patients following both scans. Furthermore, we found significant associations between the Expanded Disability Status Scale and the rsFC of the left DCP with the DLPFC and parietal areas in RRMS patients. Our results suggest that the DCP may be a critical striatal subregion in the pathophysiology of RRMS.

摘要

异常的皮质纹状体静息态功能连接(rsFC)与多发性硬化症的神经病理学有关。纹状体是基底神经节的一个组成部分,参与多种功能,包括运动、认知、情感和边缘信息处理。然而,复发缓解型多发性硬化症(RRMS)患者中导致rsFC变化的纹状体亚区域的脑回路仍不清楚。我们将每个半球的纹状体六个亚区作为种子,来研究RRMS患者与匹配的健康对照(HCs)之间纹状体亚区的rsFC。此外,我们还对一组RRMS患者在平均7个月后进行了扫描,以检验我们研究结果的可靠性。与HCs相比,我们发现在两次扫描后,RRMS患者的背侧尾状壳核(DCP)与运动前区、背外侧前额叶皮质(DLPFC)、脑岛、楔前叶和顶上小叶的连接显著增加,并且腹侧上纹状体与后扣带回皮质(PCC)之间的连接也显著增加。此外,我们发现RRMS患者的扩展残疾状态量表与左侧DCP和DLPFC及顶叶区域的rsFC之间存在显著关联。我们的结果表明,DCP可能是RRMS病理生理学中的一个关键纹状体亚区。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/55cb5afe7a36/fneur-08-00129-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/913bb231bcbb/fneur-08-00129-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/7b8486e0a6d5/fneur-08-00129-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/b8f14e2f32eb/fneur-08-00129-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/544b2d850725/fneur-08-00129-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/554a7d47c0e2/fneur-08-00129-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/55cb5afe7a36/fneur-08-00129-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/913bb231bcbb/fneur-08-00129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/9ce0d875ad28/fneur-08-00129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/7b8486e0a6d5/fneur-08-00129-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/b8f14e2f32eb/fneur-08-00129-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/544b2d850725/fneur-08-00129-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/554a7d47c0e2/fneur-08-00129-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80d/5401875/55cb5afe7a36/fneur-08-00129-g007.jpg

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