基于稀疏高斯贝叶斯网络的判别性脑有效连通性分析。

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引用次数: 16

摘要

从神经图像中分析大脑网络正在成为识别阿尔茨海默病(AD)的新型基于连接的生物标志物的一种有前途的方法。在这方面,研究大脑区域之间因果关系的大脑“有效连通性”分析具有很高的挑战性和许多研究机会。该领域的现有工作大多使用生成方法。尽管生成方法在数据表示和其他重要优点方面取得了成功,但它们不一定具有判别性,这可能导致对细微但关键的疾病引起的变化的忽视。在本文中,我们提出了一种基于学习的方法,该方法集成了生成和判别方法的优点,以恢复有效的连通性。特别地,我们使用Fisher核来桥接稀疏贝叶斯网络(SBN)的生成模型和svm的判别分类器,并通过最小化svm的泛化误差界将SBN参数学习转换为Fisher核学习。该方法能够同时提高生成式SBN模型和基于Fisher核的SBN诱导SVM分类器的识别能力。利用ADNI数据对该方法进行了脑有效连通性分析。它显示了对最先进的技术的显著改进:我们的SBN模型的分类精度提高了10%以上,我们的SBN诱导的SVM分类器通过简单的特征选择提高了16%以上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discriminative Brain Effective Connectivity Analysis for Alzheimer's Disease: A Kernel Learning Approach upon Sparse Gaussian Bayesian Network.

Analyzing brain network from neuroimages is becoming a promising approach in identifying novel connectivity-based biomarkers for the Alzheimer's disease (AD). In this regard, brain "effective connectivity" analysis, which studies the causal relationship among brain regions, is highly challenging and of many research opportunities. Most of the existing works in this field use generative methods. Despite their success in data representation and other important merits, generative methods are not necessarily discriminative, which may cause the ignorance of subtle but critical disease-induced changes. In this paper, we propose a learning-based approach that integrates the benefits of generative and discriminative methods to recover effective connectivity. In particular, we employ Fisher kernel to bridge the generative models of sparse Bayesian network (SBN) and the discriminative classifiers of SVMs, and convert the SBN parameter learning to Fisher kernel learning via minimizing a generalization error bound of SVMs. Our method is able to simultaneously boost the discrimination power of both the generative SBN models and the SBN-induced SVM classifiers via Fisher kernel. The proposed method is tested on analyzing brain effective connectivity for AD from ADNI data. It demonstrates significant improvements over the state-of-the-art: classification accuracy increased above 10% by our SBN models, and above 16% by our SBN-induced SVM classifiers with a simple feature selection.

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