Li Zeming, Xu Yu, Chowdhury Debajyoti, Yip Hip Fung, Wang Chonghao, Zhang Lu
Department of Computer Science, Hong Kong Baptist University, Hong Kong, 999077, China.
School of Chinese Medicine, Hong Kong Baptist University, Hong Kong, 999077, China.
Interdiscip Sci. 2025 Sep 17. doi: 10.1007/s12539-025-00749-9.
Traditional disease risk prediction models predominantly rely on statistical algorithms and often focus on genetic factors or a limited set of lifestyle factors to estimate the risk of disease onset. Recently, more comprehensive approaches have emerged that integrate genetic factors with additional lifestyle factors (e.g., alcohol intake) and physical features (e.g., body mass index, age) to increase predictive accuracy. Since the onset of complex diseases is often accompanied by the occurrence of comorbidities, incorporating medical history records is a critical yet underexplored avenue for improving risk prediction. In this study, we propose a novel framework, MIDRP (Multi-source Integration for Disease Risk Prediction), which incorporates genetic variants, lifestyle factors, physical attributes, and medical history records to achieve more robust and accurate predictions. At the heart of our approach lies a causal Transformer architecture, specifically designed to extract and interpret nuanced patterns from medical history records. In the experiments, we compared MIDRP with several baselines, including LDPred2, random forest, multilayer perception, logistic regression, AdaBoost, DiseaseCapsule, EIR, and Med-Bert, on three complex diseases Coronary Artery Disease, Type 2 Diabetes, and Breast Cancer using data from the UK Biobank. Our method achieved state-of-the-art performance, AUROC scores of 0.783, 0.841, and 0.784, respectively, demonstrating its potential in the field of complex disease risk prediction.
传统的疾病风险预测模型主要依赖统计算法,并且通常侧重于遗传因素或一组有限的生活方式因素来估计疾病发病风险。最近,出现了更全面的方法,这些方法将遗传因素与其他生活方式因素(如酒精摄入量)和身体特征(如体重指数、年龄)相结合,以提高预测准确性。由于复杂疾病的发病往往伴随着合并症的发生,纳入病史记录是改善风险预测的一个关键但尚未充分探索的途径。在本研究中,我们提出了一个新颖的框架,即MIDRP(疾病风险预测的多源整合),它整合了基因变异、生活方式因素、身体属性和病史记录,以实现更稳健和准确的预测。我们方法的核心是一种因果Transformer架构,专门设计用于从病史记录中提取和解释细微的模式。在实验中,我们使用来自英国生物银行的数据,将MIDRP与几个基线方法进行了比较,包括LDPred2、随机森林、多层感知器、逻辑回归、AdaBoost、DiseaseCapsule、EIR和Med-Bert,针对三种复杂疾病:冠状动脉疾病、2型糖尿病和乳腺癌。我们的方法取得了领先的性能,在这三种疾病上的AUROC分数分别为0.783、0.841和0.784,证明了其在复杂疾病风险预测领域的潜力。