利用稀疏高斯贝叶斯网络为阿尔茨海默病建立大脑有效连接性模型

Shuai Huang, Jing Li, Jieping Ye, Adam Fleisher, Kewei Chen, Teresa Wu, Eric Reiman
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摘要

最近的研究表明,阿尔茨海默病(AD)与大脑连接网络的改变有关。其中一种连通性被称为有效连通性,定义为大脑区域之间的定向关系,对大脑功能至关重要。然而,关于建立 AD 的有效连通性模型并描述其与正常对照组(NC)的差异的研究还很少。在本文中,我们研究了用于有效连接建模的稀疏贝叶斯网络(BN)。具体来说,我们提出了一种新颖的贝叶斯网络结构学习方法,其中包括一个 L1 准则惩罚项来施加稀疏性,以及另一个惩罚项来确保学习到的贝叶斯网络是一个有向无环图--这是贝叶斯网络的一个必要属性。我们通过理论分析和在 11 个具有不同样本量的中型和大型基准网络上进行的大量实验表明,与 10 种竞争算法相比,所提出的方法在学习准确性和可扩展性方面都有很大改进。我们将提出的方法应用于 42 名 AD 和 67 名 NC 受试者的 FDG-PET 图像,并分别确定了 AD 和 NC 的有效连接模型。我们的研究发现,AD 和 NC 的有效连通性在很多方面都不同,包括全局范围的有效连通性、叶内、叶间和半球间的有效连通性分布,以及与特定脑区相关的有效连通性。这些发现与AD的已知病理和临床进展一致,将有助于AD知识的发现。
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Brain Effective Connectivity Modeling for Alzheimer's Disease by Sparse Gaussian Bayesian Network.

Recent studies have shown that Alzheimer's disease (AD) is related to alteration in brain connectivity networks. One type of connectivity, called effective connectivity, defined as the directional relationship between brain regions, is essential to brain function. However, there have been few studies on modeling the effective connectivity of AD and characterizing its difference from normal controls (NC). In this paper, we investigate the sparse Bayesian Network (BN) for effective connectivity modeling. Specifically, we propose a novel formulation for the structure learning of BNs, which involves one L1-norm penalty term to impose sparsity and another penalty to ensure the learned BN to be a directed acyclic graph - a required property of BNs. We show, through both theoretical analysis and extensive experiments on eleven moderate and large benchmark networks with various sample sizes, that the proposed method has much improved learning accuracy and scalability compared with ten competing algorithms. We apply the proposed method to FDG-PET images of 42 AD and 67 NC subjects, and identify the effective connectivity models for AD and NC, respectively. Our study reveals that the effective connectivity of AD is different from that of NC in many ways, including the global-scale effective connectivity, intra-lobe, interlobe, and inter-hemispheric effective connectivity distributions, as well as the effective connectivity associated with specific brain regions. These findings are consistent with known pathology and clinical progression of AD, and will contribute to AD knowledge discovery.

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