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运用连接组学绘制阿尔茨海默病大脑图谱。

Mapping the Alzheimer's brain with connectomics.

作者信息

Xie Teng, He Yong

机构信息

State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University Beijing, China.

出版信息

Front Psychiatry. 2012 Jan 5;2:77. doi: 10.3389/fpsyt.2011.00077. eCollection 2011.

DOI:10.3389/fpsyt.2011.00077
PMID:22291664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3251821/
Abstract

Alzheimer's disease (AD) is the most common form of dementia. As an incurable, progressive, and neurodegenerative disease, it causes cognitive and memory deficits. However, the biological mechanisms underlying the disease are not thoroughly understood. In recent years, non-invasive neuroimaging and neurophysiological techniques [e.g., structural magnetic resonance imaging (MRI), diffusion MRI, functional MRI, and EEG/MEG] and graph theory based network analysis have provided a new perspective on structural and functional connectivity patterns of the human brain (i.e., the human connectome) in health and disease. Using these powerful approaches, several recent studies of patients with AD exhibited abnormal topological organization in both global and regional properties of neuronal networks, indicating that AD not only affects specific brain regions, but also alters the structural and functional associations between distinct brain regions. Specifically, disruptive organization in the whole-brain networks in AD is involved in the loss of small-world characters and the re-organization of hub distributions. These aberrant neuronal connectivity patterns were associated with cognitive deficits in patients with AD, even with genetic factors in healthy aging. These studies provide empirical evidence to support the existence of an aberrant connectome of AD. In this review we will summarize recent advances discovered in large-scale brain network studies of AD, mainly focusing on graph theoretical analysis of brain connectivity abnormalities. These studies provide novel insights into the pathophysiological mechanisms of AD and could be helpful in developing imaging biomarkers for disease diagnosis and monitoring.

摘要

阿尔茨海默病(AD)是最常见的痴呆形式。作为一种无法治愈、进行性的神经退行性疾病,它会导致认知和记忆缺陷。然而,该疾病背后的生物学机制尚未被完全理解。近年来,非侵入性神经影像学和神经生理学技术[例如,结构磁共振成像(MRI)、扩散MRI、功能MRI以及脑电图/脑磁图(EEG/MEG)]和基于图论的网络分析为健康和疾病状态下人类大脑的结构和功能连接模式(即人类连接组)提供了新的视角。使用这些强大的方法,最近几项针对AD患者的研究显示,神经元网络的全局和区域特性均存在异常拓扑组织,这表明AD不仅影响特定脑区,还会改变不同脑区之间的结构和功能关联。具体而言,AD患者全脑网络中的紊乱组织涉及小世界特征的丧失和枢纽分布重新组织。这些异常的神经元连接模式与AD患者的认知缺陷相关,甚至与健康衰老中的遗传因素也有关联。这些研究为支持AD异常连接组的存在提供了实证依据。在本综述中,我们将总结AD大规模脑网络研究中发现的最新进展,主要聚焦于脑连接异常的图论分析。这些研究为AD的病理生理机制提供了新的见解,并可能有助于开发用于疾病诊断和监测的成像生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/91361d4bbb7c/fpsyt-02-00077-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/efc7ec43d7b8/fpsyt-02-00077-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/458bff336ffb/fpsyt-02-00077-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/10a77a20de60/fpsyt-02-00077-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/91361d4bbb7c/fpsyt-02-00077-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/efc7ec43d7b8/fpsyt-02-00077-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/458bff336ffb/fpsyt-02-00077-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/10a77a20de60/fpsyt-02-00077-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/3251821/91361d4bbb7c/fpsyt-02-00077-g004.jpg

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Altered connectivity pattern of hubs in default-mode network with Alzheimer's disease: an Granger causality modeling approach.阿尔茨海默病患者默认模式网络中枢纽节点连接模式的改变:基于 Granger 因果关系建模方法的研究。
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Network centrality in the human functional connectome.
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