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Discovering Aberrant Patterns of Human Connectome in Alzheimer's Disease via Subgraph Mining

机译:通过子画面挖掘发现阿尔茨海默病的人类联系的异常模式

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Alzheimer's disease (AD) is the most common cause of age-related dementia, which prominently affects the human connectome. Diffusion weighted imaging (DWI) provides a promising way to explore the organization of white matter fiber tracts in the human brain in a non-invasive way. However, the immense amount of data from millions of voxels of a raw diffusion map prevent an easy way to utilizable knowledge. In this paper, we focus on the question how we can identify disrupted spatial patterns of the human connectome in AD based on a data mining framework. Using diffusion tractography, the human connectomes for each individual subject were constructed based on two diffusion derived attributes: fiber density and fractional anisotropy, to represent the structural brain connectivity patterns. Then, these humanconnectomes were further mapped into a series of unweighted graphs by discretization. After frequent sub graph mining, the abnormal score was finally defined to identify disrupted sub graph patterns in patients. Experiments demonstrated that our data-driven approach, for the first time, allows identifying selective spatial pattern changes of the human connectome in AD that perfectly matched grey matter changes of the disease. Our findings further bring new insights into how AD propagates and disrupts the regional integrity of large-scale structural brain networks in a fiber connectivity-based way.
机译:阿尔茨海默病(AD)是与年龄相关的痴呆症最常见的原因,这突出地影响了人类的连接。扩散加权成像(DWI)提供了一种有希望以非侵入性方式探索人脑中白质纤维毛虫的组织。然而,来自原始扩散图的数百万个体素的巨大数据阻碍了可利用的知识的简单方法。在本文中,我们专注于如何根据数据挖掘框架识别人类联系中断的空间模式。使用扩散牵引术,基于两个扩散衍生的属性构建每个单独对象的人Connectomes:纤维密度和分数各向异性,以表示结构脑连接模式。然后,通过离散化进一步映射到一系列未加权的图表中。经常常见的子图挖掘后,最终定义异常得分以识别患者中断的子图形模式。实验表明,我们的数据驱动方法首次允许在广告中识别人类连接的选择性空间变化,这与疾病的灰质变化完全匹配。我们的调查结果进一步提出了新的见解,以广告传播和扰乱基于光纤连接的大规模结构脑网络的区域完整性。

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