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基于深度自重建融合相似性哈希的多模态数据阿尔茨海默病诊断方法。

Deep Self-Reconstruction Fusion Similarity Hashing for the Diagnosis of Alzheimer's Disease on Multi-Modal Data.

出版信息

IEEE J Biomed Health Inform. 2024 Jun;28(6):3513-3522. doi: 10.1109/JBHI.2024.3383885. Epub 2024 Jun 6.

DOI:10.1109/JBHI.2024.3383885
PMID:38568771
Abstract

The pathogenesis of Alzheimer's disease (AD) is extremely intricate, which makes AD patients almost incurable. Recent studies have demonstrated that analyzing multi-modal data can offer a comprehensive perspective on the different stages of AD progression, which is beneficial for early diagnosis of AD. In this paper, we propose a deep self-reconstruction fusion similarity hashing (DS-FSH) method to effectively capture the AD-related biomarkers from the multi-modal data and leverage them to diagnose AD. Given that most existing methods ignore the topological structure of the data, a deep self-reconstruction model based on random walk graph regularization is designed to reconstruct the multi-modal data, thereby learning the nonlinear relationship between samples. Additionally, a fused similarity hash based on anchor graph is proposed to generate discriminative binary hash codes for multi-modal reconstructed data. This allows sample fused similarity to be effectively modeled by a fusion similarity matrix based on anchor graph while modal correlation can be approximated by Hamming distance. Especially, extracted features from the multi-modal data are classified using deep sparse autoencoders classifier. Finally, experiments conduct on the AD Neuroimaging Initiative database show that DS-FSH outperforms comparable methods of AD classification. To conclude, DS-FSH identifies multi-modal features closely associated with AD, which are expected to contribute significantly to understanding of the pathogenesis of AD.

摘要

阿尔茨海默病(AD)的发病机制极其复杂,这使得 AD 患者几乎无法治愈。最近的研究表明,分析多模态数据可以提供 AD 进展不同阶段的综合视角,有利于 AD 的早期诊断。在本文中,我们提出了一种深度自重建融合相似性哈希(DS-FSH)方法,以有效地从多模态数据中提取与 AD 相关的生物标志物,并利用这些生物标志物来诊断 AD。鉴于大多数现有方法忽略了数据的拓扑结构,我们设计了一种基于随机游走图正则化的深度自重建模型来重建多模态数据,从而学习样本之间的非线性关系。此外,我们提出了一种基于锚图的融合相似性哈希方法,为多模态重建数据生成有鉴别力的二进制哈希码。这使得基于锚图的融合相似性矩阵能够有效地对样本融合相似性进行建模,而模态相关性可以通过汉明距离来近似。特别是,使用深度稀疏自动编码器分类器对多模态数据提取的特征进行分类。最后,在 AD 神经影像学倡议数据库上进行的实验表明,DS-FSH 在 AD 分类方面优于可比的方法。总之,DS-FSH 识别出与 AD 密切相关的多模态特征,有望对 AD 发病机制的理解做出重大贡献。

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