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颞叶-小脑有效连接的改变能够有效区分稳定型和进展型轻度认知障碍。

Alteration in temporal-cerebellar effective connectivity can effectively distinguish stable and progressive mild cognitive impairment.

作者信息

Xue Chen, Zheng Darui, Ruan Yiming, Guo Wenxuan, Hu Jun

机构信息

Department of Radiology, The Affiliated Brain Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Front Aging Neurosci. 2024 Aug 29;16:1442721. doi: 10.3389/fnagi.2024.1442721. eCollection 2024.

DOI:10.3389/fnagi.2024.1442721
PMID:39267723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11390694/
Abstract

BACKGROUND

Stable mild cognitive impairment (sMCI) and progressive mild cognitive impairment (pMCI) represent two distinct subtypes of mild cognitive impairment (MCI). Early and effective diagnosis and accurate differentiation between sMCI and pMCI are crucial for administering targeted early intervention and preventing cognitive decline. This study investigated the intrinsic dysconnectivity patterns in sMCI and pMCI based on degree centrality (DC) and effective connectivity (EC) analyses, with the goal of uncovering shared and distinct neuroimaging mechanisms between subtypes.

METHODS

Resting-state functional magnetic resonance imaging combined with DC analysis was used to explore the functional connectivity density in 42 patients with sMCI, 31 patients with pMCI, and 82 healthy control (HC) participants. Granger causality analysis was used to assess changes in EC based on the significant clusters found in DC. Furthermore, correlation analysis was conducted to examine the associations between altered DC/EC values and cognitive function. Receiver operating characteristic curve analysis was performed to determine the accuracy of abnormal DC and EC values in distinguishing sMCI from pMCI.

RESULTS

Compared with the HC group, both pMCI and sMCI groups exhibited increased DC in the left inferior temporal gyrus (ITG), left posterior cerebellum lobe (CPL), and right cerebellum anterior lobe (CAL), along with decreased DC in the left medial frontal gyrus. Moreover, the sMCI group displayed reduced EC from the right CAL to bilateral CPL, left superior temporal gyrus, and bilateral caudate compared with HC. pMCI demonstrated elevated EC from the right CAL to left ITG, which was linked to episodic memory and executive function. Notably, the EC from the right CAL to the right ITG effectively distinguished sMCI from pMCI, with sensitivity, specificity, and accuracy of 0.5806, 0.9512, and 0.828, respectively.

CONCLUSION

This study uncovered shared and distinct alterations in DC and EC between sMCI and pMCI, highlighting their involvement in cognitive function. Of particular significance are the unidirectional EC disruptions from the cerebellum to the temporal lobe, which serve as a discriminating factor between sMCI and pMCI and provide a new perspective for understanding the temporal-cerebellum. These findings offer novel insights into the neural circuit mechanisms involving the temporal-cerebellum connection in MCI.

摘要

背景

稳定型轻度认知障碍(sMCI)和进展型轻度认知障碍(pMCI)是轻度认知障碍(MCI)的两种不同亚型。早期有效诊断以及sMCI和pMCI之间的准确区分对于实施有针对性的早期干预和预防认知衰退至关重要。本研究基于度中心性(DC)和有效连接性(EC)分析,探究sMCI和pMCI中的内在失连接模式,旨在揭示各亚型之间共同的和独特的神经影像学机制。

方法

采用静息态功能磁共振成像结合DC分析,探索42例sMCI患者、31例pMCI患者和82名健康对照(HC)参与者的功能连接密度。基于DC中发现的显著簇,使用格兰杰因果分析评估EC的变化。此外,进行相关性分析以检验DC/EC值改变与认知功能之间的关联。进行受试者工作特征曲线分析,以确定异常DC和EC值在区分sMCI和pMCI方面的准确性。

结果

与HC组相比,pMCI组和sMCI组在左侧颞下回(ITG)、左侧小脑后叶(CPL)和右侧小脑前叶(CAL)的DC均增加,而左侧额内侧回的DC降低。此外,与HC相比,sMCI组从右侧CAL到双侧CPL、左侧颞上回和双侧尾状核的EC降低。pMCI显示从右侧CAL到左侧ITG的EC升高,这与情景记忆和执行功能相关。值得注意的是,从右侧CAL到右侧ITG的EC有效地区分了sMCI和pMCI,敏感性、特异性和准确性分别为0.5806、0.9512和0.828。

结论

本研究揭示了sMCI和pMCI在DC和EC方面共同的和独特的改变,突出了它们在认知功能中的作用。特别重要的是从小脑到颞叶的单向EC破坏,这是区分sMCI和pMCI的一个因素,并为理解颞叶 - 小脑提供了新的视角。这些发现为MCI中涉及颞叶 - 小脑连接的神经回路机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/86956f66ac50/fnagi-16-1442721-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/111b40b29e16/fnagi-16-1442721-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/ad192fc89118/fnagi-16-1442721-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/7e8dbafaed9c/fnagi-16-1442721-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/86956f66ac50/fnagi-16-1442721-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/111b40b29e16/fnagi-16-1442721-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/ad192fc89118/fnagi-16-1442721-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/7e8dbafaed9c/fnagi-16-1442721-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67b/11390694/86956f66ac50/fnagi-16-1442721-g004.jpg

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