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Multivariate Deep Learning Classification of Alzheimer’s Disease Based on Hierarchical Partner Matching Independent Component Analysis

机译:基于分层合作伙伴匹配独立成分分析的阿尔茨海默病多元深度学习分类

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摘要

Machine learning and pattern recognition have been widely investigated in order to look for the biomarkers of Alzheimer’s disease (AD). However, most existing methods extract features by seed-based correlation, which not only requires prior information but also ignores the relationship between resting state functional magnetic resonance imaging (rs-fMRI) voxels. In this study, we proposed a deep learning classification framework with multivariate data-driven based feature extraction for automatic diagnosis of AD. Specifically, a three-level hierarchical partner matching independent components analysis (3LHPM-ICA) approach was proposed first in order to address the issues in spatial individual ICA, including the uncertainty of the numbers of components, the randomness of initial values, and the correspondence of ICs of multiple subjects, resulting in stable and reliable ICs which were applied as the intrinsic brain functional connectivity (FC) features. Second, Granger causality (GC) was utilized to infer directional interaction between the ICs that were identified by the 3LHPM-ICA method and extract the effective connectivity features. Finally, a deep learning classification framework was developed to distinguish AD from controls by fusing the functional and effective connectivities. A resting state fMRI dataset containing 34 AD patients and 34 normal controls (NCs) was applied to the multivariate deep learning platform, leading to a classification accuracy of 95.59%, with a sensitivity of 97.06% and a specificity of 94.12% with leave-one-out cross validation (LOOCV). The experimental results demonstrated that the measures of neural connectivities of ICA and GC followed by deep learning classification represented the most powerful methods of distinguishing AD clinical data from NCs, and these aberrant brain connectivities might serve as robust brain biomarkers for AD. This approach also allows for expansion of the methodology to classify other psychiatric disorders.
机译:机器学习和模式识别已被广泛研究,以寻找阿尔茨海默氏病(AD)的生物标记。然而,大多数现有方法通过基于种子的相关性来提取特征,这不仅需要先验信息,而且还忽略了静止状态功能磁共振成像(rs-fMRI)体素之间的关系。在这项研究中,我们提出了一种基于多元数据驱动的特征提取的深度学习分类框架,用于AD的自动诊断。具体来说,为了解决空间个体ICA中的问题,首先提出了三级分层伙伴匹配独立成分分析(3LHPM-ICA)方法,包括成分数量的不确定性,初始值的随机性和对应性。可以将多个受试者的IC集成在一起,从而获得稳定可靠的IC,这些IC被用作固有的大脑功能连接(FC)功能。其次,利用格兰杰因果关系(GC)来推断通过3LHPM-ICA方法识别的IC之间的方向交互,并提取有效的连通性特征。最后,开发了深度学习分类框架,通过融合功能和有效的连接性来区分AD与控件。将包含34位AD患者和34位正常对照(NC)的静止状态fMRI数据集应用于多元深度学习平台,分类精度为95.59%,灵敏度为97.06%,特异度为94.12%(留一)出站交叉验证(LOOCV)。实验结果表明,ICA和GC的神经连接性测量以及深度学习分类是区分AD临床数据和NCs的最有效方法,这些异常的大脑连接性可以作为AD的强大脑生物标志物。这种方法还允许扩展对其他精神疾病进行分类的方法。

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