Dai Zhengjia, Yan Chaogan, Li Kuncheng, Wang Zhiqun, Wang Jinhui, Cao Miao, Lin Qixiang, Shu Ni, Xia Mingrui, Bi Yanchao, He Yong
State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research Center for Collaboration and Innovation in Brain and Learning Sciences, Beijing Normal University, Beijing 100875, China.
State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research Nathan Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.
Cereb Cortex. 2015 Oct;25(10):3723-42. doi: 10.1093/cercor/bhu246. Epub 2014 Oct 19.
Alzheimer's disease (AD) is associated not only with regional gray matter damages, but also with abnormalities in functional integration between brain regions. Here, we employed resting-state functional magnetic resonance imaging data and voxel-based graph-theory analysis to systematically investigate intrinsic functional connectivity patterns of whole-brain networks in 32 AD patients and 38 healthy controls (HCs). We found that AD selectively targeted highly connected hub regions (in terms of nodal functional connectivity strength) of brain networks, involving the medial and lateral prefrontal and parietal cortices, insula, and thalamus. This impairment was connectivity distance-dependent (Euclidean), with the most prominent disruptions appearing in the long-range connections (e.g., 100-130 mm). Moreover, AD also disrupted functional connections within the default-mode, salience and executive-control modules, and connections between the salience and executive-control modules. These disruptions of hub connectivity and modular integrity significantly correlated with the patients' cognitive performance. Finally, the nodal connectivity strength in the posteromedial cortex exhibited a highly discriminative power in distinguishing individuals with AD from HCs. Taken together, our results emphasize AD-related degeneration of specific brain hubs, thus providing novel insights into the pathophysiological mechanisms of connectivity dysfunction in AD and suggesting the potential of using network hub connectivity as a diagnostic biomarker.
阿尔茨海默病(AD)不仅与局部灰质损伤有关,还与脑区之间功能整合异常有关。在此,我们采用静息态功能磁共振成像数据和基于体素的图论分析,系统研究了32例AD患者和38名健康对照(HCs)全脑网络的内在功能连接模式。我们发现,AD选择性地靶向脑网络中高度连接的枢纽区域(根据节点功能连接强度),涉及内侧和外侧前额叶及顶叶皮质、岛叶和丘脑。这种损害与连接距离相关(欧几里得距离),最显著的破坏出现在长程连接中(例如100 - 130毫米)。此外,AD还破坏了默认模式、突显和执行控制模块内的功能连接,以及突显和执行控制模块之间的连接。这些枢纽连接性和模块完整性的破坏与患者的认知表现显著相关。最后,后内侧皮质的节点连接强度在区分AD患者和HCs个体方面表现出高度的判别能力。综上所述,我们的结果强调了与AD相关的特定脑枢纽的退化,从而为AD中连接功能障碍的病理生理机制提供了新的见解,并提示了将网络枢纽连接性用作诊断生物标志物的潜力。