The brain network hub degeneration in Alzheimer's disease.

Suhui Jin, Jinhui Wang, Yong He
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Abstract

Alzheimer's disease (AD) has been conceptualized as a syndrome of brain network dysfunction. Recent imaging connectomics studies have provided unprecedented opportunities to map structural and functional brain networks in AD. By reviewing molecular, imaging, and computational modeling studies, we have shown that highly connected brain hubs are primarily distributed in the medial and lateral prefrontal, parietal, and temporal regions in healthy individuals and that the hubs are selectively and severely affected in AD as manifested by increased amyloid-beta deposition and regional atrophy, hypo-metabolism, and connectivity dysfunction. Furthermore, AD-related hub degeneration depends on the imaging modality with the most notable degeneration in the medial temporal hubs for morphological covariance networks, the prefrontal hubs for structural white matter networks, and in the medial parietal hubs for functional networks. Finally, the AD-related hub degeneration shows metabolic, molecular, and genetic correlates. Collectively, we conclude that the brain-network-hub-degeneration framework is promising to elucidate the biological mechanisms of network dysfunction in AD, which provides valuable information on potential diagnostic biomarkers and promising therapeutic targets for the disease.

阿尔茨海默病的大脑网络中枢退化。
阿尔茨海默病(AD)被认为是一种大脑网络功能障碍综合征。最近的成像连接组学研究为绘制阿尔茨海默病的大脑结构和功能网络图提供了前所未有的机会。通过回顾分子、成像和计算建模研究,我们发现高度连接的大脑中枢主要分布在健康人的内侧和外侧前额叶、顶叶和颞叶区域,而这些中枢在AD中会受到选择性的严重影响,表现为淀粉样蛋白-β沉积增加、区域萎缩、代谢低下和连接功能障碍。此外,与AD相关的中枢变性取决于成像模式,其中形态学协方差网络中的颞叶内侧中枢、结构性白质网络中的前额叶中枢以及功能性网络中的顶叶内侧中枢的变性最为显著。最后,AD 相关中枢退化显示出代谢、分子和遗传相关性。总之,我们得出结论:大脑-网络-中枢-退化框架有望阐明AD网络功能障碍的生物学机制,从而为该疾病的潜在诊断生物标记物和治疗靶点提供有价值的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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