多模态注意力融合深度自我重建呈现模型用于阿尔茨海默病诊断和生物标志物识别。

IF 4.5 3区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Shan Huang, Yixin Liu, Jingyu Zhang, Yiming Wang
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引用次数: 0

摘要

阿尔茨海默病(AD)的未知致病机制使治疗具有挑战性。神经影像遗传学为早期诊断提供了一种识别疾病生物标志物的方法,但传统方法难以处理复杂的非线性、多模态和多表达数据。然而,传统的关联分析方法在处理非线性、多模态和多表达数据时面临挑战。为此,提出了一种多模态注意力融合深度自重构表示(MAFDSRP)模型来解决上述问题。首先,采用一种新颖的直方图匹配多注意机制对多模态脑成像数据进行处理,动态调整各输入脑图像数据的权重;同时,对遗传数据进行预处理,去除低质量样本。随后,将遗传数据和融合后的神经影像学数据分别输入到自重构网络中学习非线性关系,并在网络顶层进行子空间聚类。最后,通过表达关联分析对学习到的遗传数据和融合的神经影像学数据进行分析,以识别ad相关的生物标志物。鉴定出的生物标志物进行了系统的多层次分析,揭示了生物标志物在分子、组织和功能水平上的作用,突出了与AD相关的炎症、脂质代谢、记忆和情绪处理等过程。实验结果表明,MAFDSRP在关联分析中达到0.58,显示了其在准确识别ad相关生物标志物方面的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal attention fusion deep self-reconstruction presentation model for Alzheimer's disease diagnosis and biomarker identification.

The unknown pathogenic mechanisms of Alzheimer's disease (AD) make treatment challenging. Neuroimaging genetics offers a method for identifying disease biomarkers for early diagnosis, but traditional approaches struggle with complex non-linear, multimodal and multi-expression data. However, traditional association analysis methods face challenges in handling nonlinear, multimodal and multi-expression data. Therefore, a multimodal attention fusion deep self-restructuring presentation (MAFDSRP) model is proposed to solve the above problem. First, multimodal brain imaging data are processed through a novel histogram-matching multiple attention mechanisms to dynamically adjust the weight of each input brain image data. Simultaneous, the genetic data are preprocessed to remove low-quality samples. Subsequently, the genetic data and fused neuroimaging data are separately input into the self-reconstruction network to learn the nonlinear relationships and perform subspace clustering at the top layer of the network. Finally, the learned genetic data and fused neuroimaging data are analysed through expression association analysis to identify AD-related biomarkers. The identified biomarkers underwent systematic multi-level analysis, revealing biomarker roles at molecular, tissue and functional levels, highlighting processes like inflammation, lipid metabolism, memory and emotional processing linked to AD. The experimental results show that MAFDSRP achieved 0.58 in association analysis, demonstrating its great potential in accurately identifying AD-related biomarkers.

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来源期刊
Artificial Cells, Nanomedicine, and Biotechnology
Artificial Cells, Nanomedicine, and Biotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ENGINEERING, BIOMEDICAL
CiteScore
10.90
自引率
0.00%
发文量
48
审稿时长
20 weeks
期刊介绍: Artificial Cells, Nanomedicine and Biotechnology covers the frontiers of interdisciplinary research and application, combining artificial cells, nanotechnology, nanobiotechnology, biotechnology, molecular biology, bioencapsulation, novel carriers, stem cells and tissue engineering. Emphasis is on basic research, applied research, and clinical and industrial applications of the following topics:artificial cellsblood substitutes and oxygen therapeuticsnanotechnology, nanobiotecnology, nanomedicinetissue engineeringstem cellsbioencapsulationmicroencapsulation and nanoencapsulationmicroparticles and nanoparticlesliposomescell therapy and gene therapyenzyme therapydrug delivery systemsbiodegradable and biocompatible polymers for scaffolds and carriersbiosensorsimmobilized enzymes and their usesother biotechnological and nanobiotechnological approachesRapid progress in modern research cannot be carried out in isolation and is based on the combined use of the different novel approaches. The interdisciplinary research involving novel approaches, as discussed above, has revolutionized this field resulting in rapid developments. This journal serves to bring these different, modern and futuristic approaches together for the academic, clinical and industrial communities to allow for even greater developments of this highly interdisciplinary area.
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