Causal Transformer for Learning Embeddings from Structured Medical History Records and Multi-Source Data Integration for Complex Disease Risk Prediction

  • Zeming Li
  • , Yu Xu
  • , Debajyoti Chowdhury
  • , Hip Fung Yip
  • , Chonghao Wang
  • , Lu Zhang*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

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.

Original languageEnglish
Number of pages14
JournalInterdisciplinary Sciences - Computational Life Sciences
DOIs
Publication statusE-pub ahead of print - 17 Sept 2025

User-Defined Keywords

  • Deep learning
  • Genome wide association study
  • Medical history record
  • Polygenic risk score
  • Single nucleotide polymorphism

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