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Integrating Functional and Structural Connectivities via Diffusion-Convolution-Bilinear Neural Network

机译:通过扩散-卷积-双线性神经网络整合功能和结构连通性

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Traditional brain network methods usually focus on either functional connectivity (FC) or structural connectivity (SC) for describing node interactions and only consider the interaction between paired network nodes. Therefore, the underlying relationship between FC and SC, as well as the complicated interactions among network nodes, has not been sufficiently studied and fully utilized to discover disease-related biomarkers. To tackle these problems, we propose a Diffusion-Convolution-Bilinear Neural Network (DCB-NN) framework for brain network analysis, which couples FC and SC seamlessly and considers wider interactions among network nodes. Specifically, a brain network model (graph) is first defined, whose edges are determined by neural fiber physical connections extracted from DTI and node features are governed by brain activities extracted from fMRI. Then, based on this model, we build two DCB modules to extract multi-scale features from this brain network. Each DCB module consists of diffusion, convolution and bilinear pooling. Through diffusion guided by physical connections, the network node features not only reflect the activities in their corresponding brain regions, but also are influenced by the activities from other brain regions. These enhanced node features are nonlinearly weighed through 1-D convolution, and their second-order statistics are further extracted by bilinear pooling for disease prediction. In order to capture node interactions at multi-scale, we include two DCB modules, corresponding to one-step and two-step diffusions, respectively. The whole model is trained in an end-to-end way. Experiments on a real epilepsy dataset demonstrate the effectiveness and advantages of our proposed method.
机译:传统的大脑网络方法通常集中于功能连接(FC)或结构连接(SC)来描述节点交互,而只考虑配对网络节点之间的交互。因此,尚未充分研究和充分利用FC和SC之间的潜在关系以及网络节点之间的复杂相互作用来发现与疾病相关的生物标记。为了解决这些问题,我们提出了用于脑网络分析的扩散-卷积-双线性神经网络(DCB-NN)框架,该框架将FC和SC无缝耦合,并考虑了网络节点之间更广泛的交互。具体来说,首先定义一个大脑网络模型(图形),其边缘由从DTI提取的神经纤维物理连接确定,而节点特征则由从fMRI提取的大脑活动控制。然后,基于此模型,我们构建了两个DCB模块,以从此大脑网络中提取多尺度特征。每个DCB模块都由扩散,卷积和双线性池组成。通过物理连接指导的扩散,网络节点特征不仅反映了其相应大脑区域中的活动,而且还受到其他大脑区域中活动的影响。通过一维卷积对这些增强的节点特征进行非线性加权,并通过双线性池进一步提取其二阶统计量以进行疾病预测。为了捕获多尺度的节点交互,我们包括两个DCB模块,分别对应于一步和两步扩散。整个模型以端到端的方式进行训练。在真实的癫痫数据集上进行的实验证明了我们提出的方法的有效性和优势。

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