Multimodal adaptive fusion deep analysis model for Alzheimer's disease exploration and diagnosis.

IF 6.3 2区 医学 Q1 BIOLOGY
Yi-Ming Wang, Jingyu Zhang, Cui-Na Jiao, Bao-Min Liu, Tian-Ru Wu, Jin-Xing Liu, Shan Huang
{"title":"Multimodal adaptive fusion deep analysis model for Alzheimer's disease exploration and diagnosis.","authors":"Yi-Ming Wang, Jingyu Zhang, Cui-Na Jiao, Bao-Min Liu, Tian-Ru Wu, Jin-Xing Liu, Shan Huang","doi":"10.1016/j.compbiomed.2025.111117","DOIUrl":null,"url":null,"abstract":"<p><p>Alzheimer's disease (AD) is a chronic progressive neurodegenerative disorder, the etiology and pathogenesis of which are currently unclear. Brain imaging genetics, which analyzes genetic factors and neuroimaging phenotypic data in association, is an effective technique for identifying AD-related biomarkers. With the rapid advancement of imaging and genetic sequencing technologies, the association between multimodal imaging data and genetic data has gradually received widespread attention. However, how to make full use of the complementary information between multimodal data is an urgent problem to be solved. Therefore, Multimodal Adaptive Fusion Deep Association Analysis Model (MAFDAA) is proposed to solve the above problems. Firstly, a novel multi-head attention graph convolutional model is proposed to extract and reconstruct complementary information among multimodal data, thus constructing a comprehensive representation of brain information. Secondly, the representation module statistically encodes genetic data to obtain genetic representations, while embedding demographic information as a supplement to the genetic representation. Subsequently, in the association analysis module, nonlinear correlation analysis is conducted between genetic representations and brain reconstruction data, yielding latent association vectors for subsequent research. Finally, the diagnostic module diagnoses the subjects and identifies AD-related biomarkers based on the association analysis results. The experimental results demonstrate that MAFDAA exhibits excellent diagnostic performance. Additionally, the identified biomarkers were analyzed from different perspectives, establishing a new approach for studying the complex genetic mechanisms of neurodegenerative diseases from a micro to macro scale.</p>","PeriodicalId":10578,"journal":{"name":"Computers in biology and medicine","volume":"198 Pt A","pages":"111117"},"PeriodicalIF":6.3000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computers in biology and medicine","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.compbiomed.2025.111117","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Alzheimer's disease (AD) is a chronic progressive neurodegenerative disorder, the etiology and pathogenesis of which are currently unclear. Brain imaging genetics, which analyzes genetic factors and neuroimaging phenotypic data in association, is an effective technique for identifying AD-related biomarkers. With the rapid advancement of imaging and genetic sequencing technologies, the association between multimodal imaging data and genetic data has gradually received widespread attention. However, how to make full use of the complementary information between multimodal data is an urgent problem to be solved. Therefore, Multimodal Adaptive Fusion Deep Association Analysis Model (MAFDAA) is proposed to solve the above problems. Firstly, a novel multi-head attention graph convolutional model is proposed to extract and reconstruct complementary information among multimodal data, thus constructing a comprehensive representation of brain information. Secondly, the representation module statistically encodes genetic data to obtain genetic representations, while embedding demographic information as a supplement to the genetic representation. Subsequently, in the association analysis module, nonlinear correlation analysis is conducted between genetic representations and brain reconstruction data, yielding latent association vectors for subsequent research. Finally, the diagnostic module diagnoses the subjects and identifies AD-related biomarkers based on the association analysis results. The experimental results demonstrate that MAFDAA exhibits excellent diagnostic performance. Additionally, the identified biomarkers were analyzed from different perspectives, establishing a new approach for studying the complex genetic mechanisms of neurodegenerative diseases from a micro to macro scale.

阿尔茨海默病探索与诊断的多模态自适应融合深度分析模型。
阿尔茨海默病(AD)是一种慢性进行性神经退行性疾病,其病因和发病机制目前尚不清楚。脑成像遗传学分析遗传因素和神经成像表型数据的关联,是识别ad相关生物标志物的有效技术。随着影像技术和基因测序技术的快速发展,多模态影像数据与遗传数据之间的关联逐渐受到广泛关注。然而,如何充分利用多模态数据之间的互补信息是一个亟待解决的问题。为此,提出多模态自适应融合深度关联分析模型(MAFDAA)来解决上述问题。首先,提出了一种新的多头注意图卷积模型,提取和重构多模态数据之间的互补信息,从而构建大脑信息的综合表征;其次,表示模块对遗传数据进行统计编码,获得遗传表示,同时嵌入人口统计信息作为遗传表示的补充。随后,在关联分析模块中,对遗传表征与大脑重构数据进行非线性相关分析,得到后续研究的潜在关联向量。最后,诊断模块对受试者进行诊断,并根据关联分析结果识别ad相关的生物标志物。实验结果表明,MAFDAA具有良好的诊断性能。此外,从不同角度对鉴定的生物标志物进行分析,为从微观到宏观研究神经退行性疾病复杂的遗传机制开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Computers in biology and medicine
Computers in biology and medicine 工程技术-工程:生物医学
CiteScore
11.70
自引率
10.40%
发文量
1086
审稿时长
74 days
期刊介绍: Computers in Biology and Medicine is an international forum for sharing groundbreaking advancements in the use of computers in bioscience and medicine. This journal serves as a medium for communicating essential research, instruction, ideas, and information regarding the rapidly evolving field of computer applications in these domains. By encouraging the exchange of knowledge, we aim to facilitate progress and innovation in the utilization of computers in biology and medicine.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信