MLLIFA: Multi-level learning and interactive fusion algorithm combined with large foundation models for Alzheimer's disease diagnosis and etiology extraction
Jinxiong Fang , Da-fang Zhang , Kun Xie , Luyun Xu , Zhaoxu Xing , Xia-an Bi
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引用次数: 0
Abstract
The joint analysis of macro-level imaging and micro-level genetic information facilitates a holistic understanding of the pathological processes underlying Alzheimer's disease (AD). Although recent studies have made advances, most current approaches struggle to exploit the critical features embedded in imaging genetics data and fail to effectively reveal biological interactions. To remedy these shortcomings, this paper proposes a multi-level learning and interactive fusion framework based on large foundation models (LFMs), and accordingly develops an algorithm termed MLLIFA for the diagnosis of AD and the extraction of etiology. Specifically, MLLIFA first employs two LFMs to construct high-quality representations of brain region and gene features. Then, two sparse attention mechanisms are applied to extract key information from the constructed features. Finally, interaction learning is utilized to explore the latent relationships between features within biological contexts, guiding the effective fusion of multi-omics information. Experimental results on the ADNI dataset demonstrate that MLLIFA achieves an AD classification accuracy of 91.22%, outperforming state-of-the-art methods. Moreover, the proposed MLLIFA successfully identifies disease-related brain regions, risk genes, and brain-gene associations. These findings not only provide strong support for the precise diagnosis of AD but also offer new insights into the extraction of etiology.
宏观水平成像和微观水平遗传信息的联合分析有助于全面了解阿尔茨海默病(AD)的病理过程。尽管最近的研究取得了进展,但目前的大多数方法都难以利用成像遗传学数据中的关键特征,无法有效地揭示生物相互作用。为了弥补这些不足,本文提出了一种基于大型基础模型(large foundation models, LFMs)的多层次学习和交互融合框架,并据此开发了一种用于AD诊断和病因提取的MLLIFA算法。具体来说,MLLIFA首先使用两个LFMs来构建高质量的大脑区域和基因特征表征。然后,应用两种稀疏注意机制从构造的特征中提取关键信息。最后,利用交互学习来探索生物背景下特征之间的潜在关系,指导多组学信息的有效融合。在ADNI数据集上的实验结果表明,MLLIFA的AD分类准确率为91.22%,优于现有的分类方法。此外,所提出的MLLIFA成功地识别了疾病相关的大脑区域、风险基因和脑基因关联。这些发现不仅为AD的精确诊断提供了强有力的支持,也为病因的提取提供了新的见解。