用文献增强生成技术加速阿尔茨海默病生物标志物因果网络构建
Accelerating Causal Network Discovery of Alzheimer Disease Biomarkers via Scientific Literature-based Retrieval Augmented Generation
- 结合科学文献与检索增强生成,自动提取生物标志物及其因果关系
- 模型生成的因果边中约68%经专家评估为可靠,不确定性估计提升可信度
- 适合医学AI研究者和临床决策支持系统开发者参考
生物标志物间的因果关系对疾病诊断和治疗方案制定至关重要。以阿尔茨海默病(AD)为例,某些生物标志物可能影响其他标志物的存在,从而实现早期检测、精准分期、靶向治疗及疾病进展监测。然而,理解这些因果关系复杂且耗时,需专家分析大量文献,且存在主观偏见。本研究收集了过去25年发表的200篇AD相关论文,利用检索增强生成(RAG)技术提取AD生物标志物并生成其间的因果关系。鉴于医疗诊断的高风险性,我们引入不确定性估计评估生成因果边的可靠性,并通过自动与人工评估检验LLM推理的忠实性与科学性。结果表明,RAG提升了LLM生成更准确因果网络的能力,但整体识别性能仍有局限。本研究旨在推动基于AI的AD生物标志物因果网络发现的基础研究。
原文摘要 · Abstract (English)
The causal relationships between biomarkers are essential for disease diagnosis and medical treatment planning. One notable application is Alzheimer's disease (AD) diagnosis, where certain biomarkers may influence the presence of others, enabling early detection, precise disease staging, targeted treatments, and improved monitoring of disease progression. However, understanding these causal relationships is complex and requires extensive research. Constructing a comprehensive causal network of biomarkers demands significant effort from human experts, who must analyze a vast number of research papers, and have bias in understanding diseases' biomarkers and their relation. This raises an important question: Can advanced large language models (LLMs), such as those utilizing retrieval-augmented generation (RAG), assist in building causal networks of biomarkers for further medical analysis? To explore this, we collected 200 AD-related research papers published over the past 25 years and then integrated scientific literature with RAG to extract AD biomarkers and generate causal relations among them. Given the high-risk nature of the medical diagnosis, we applied uncertainty estimation to assess the reliability of the generated causal edges and examined the faithfulness and scientificness of LLM reasoning using both automatic and human evaluation. We find that RAG enhances the ability of LLMs to generate more accurate causal networks from scientific papers. However, the overall performance of LLMs in identifying causal relations of AD biomarkers is still limited. We hope this study will inspire further foundational research on AI-driven analysis of AD biomarkers causal network discovery.
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