Multi-Modality Disease Modeling via Collective Deep Matrix Factorization

Qi Wang, Mengying Sun, L. Zhan, P. Thompson, Shuiwang Ji, Jiayu Zhou
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引用次数: 26

Abstract

Alzheimer's disease (AD), one of the most common causes of dementia, is a severe irreversible neurodegenerative disease that results in loss of mental functions. The transitional stage between the expected cognitive decline of normal aging and AD, mild cognitive impairment (MCI), has been widely regarded as a suitable time for possible therapeutic intervention. The challenging task of MCI detection is therefore of great clinical importance, where the key is to effectively fuse predictive information from multiple heterogeneous data sources collected from the patients. In this paper, we propose a framework to fuse multiple data modalities for predictive modeling using deep matrix factorization, which explores the non-linear interactions among the modalities and exploits such interactions to transfer knowledge and enable high performance prediction. Specifically, the proposed collective deep matrix factorization decomposes all modalities simultaneously to capture non-linear structures of the modalities in a supervised manner, and learns a modality specific component for each modality and a modality invariant component across all modalities. The modality invariant component serves as a compact feature representation of patients that has high predictive power. The modality specific components provide an effective means to explore imaging genetics, yielding insights into how imaging and genotype interact with each other non-linearly in the AD pathology. Extensive empirical studies using various data modalities provided by Alzheimer's Disease Neuroimaging Initiative (ADNI) demonstrate the effectiveness of the proposed method for fusing heterogeneous modalities.
基于集体深度矩阵分解的多模态疾病建模
阿尔茨海默病(AD)是一种严重的不可逆转的神经退行性疾病,导致精神功能丧失,是痴呆症最常见的原因之一。轻度认知障碍(mild cognitive impairment, MCI)是正常衰老和AD预期认知能力下降之间的过渡阶段,被广泛认为是进行治疗干预的合适时机。因此,MCI检测的挑战性任务具有重要的临床意义,其中关键是有效融合从患者收集的多个异构数据源的预测信息。在本文中,我们提出了一个使用深度矩阵分解融合多种数据模式进行预测建模的框架,该框架探索了模式之间的非线性相互作用,并利用这种相互作用来传递知识并实现高性能预测。具体来说,提出的集体深度矩阵分解同时分解所有模态,以监督的方式捕获模态的非线性结构,并学习每个模态的模态特定成分和所有模态的模态不变成分。模态不变成分作为患者的紧凑特征表示,具有很高的预测能力。模态特异性成分为探索成像遗传学提供了有效手段,从而深入了解成像和基因型如何在AD病理中非线性地相互作用。使用阿尔茨海默病神经影像学倡议(ADNI)提供的各种数据模式进行的广泛实证研究表明,所提出的方法融合异构模式的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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