Evidence map›Paper›PMID 40963070›Full record

ArticleInterdisciplinary sciences, computational life sciences2026

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

Abstract read
In one paragraph

Article in Interdisciplinary sciences, computational life sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Computational modelling of cell identity.The Biochemical journal · 2026
    Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Zeming LiDepartment of Computer Science, Hong Kong Baptist University, Hong Kong, 999077, China.
Yu XuDepartment of Computer Science, Hong Kong Baptist University, Hong Kong, 999077, China.
Debajyoti ChowdhurySchool of Chinese Medicine, Hong Kong Baptist University, Hong Kong, 999077, China.
Hip Fung YipSchool of Chinese Medicine, Hong Kong Baptist University, Hong Kong, 999077, China.
Chonghao WangDepartment of Computer Science, Hong Kong Baptist University, Hong Kong, 999077, China.
Lu ZhangDepartment of Computer Science, Hong Kong Baptist University, Hong Kong, 999077, China. ericluzhang@hkbu.edu.hk.

Funding

Guangdong-Hong Kong Technology Cooperation Funding Scheme GHX/133/20SZHealth and Medical Research Fund 11221026Young Collaborative Research grant C2004-23Y
6 · The paper itself

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.

Indexed as

Medical History TakingAlgorithmsBreast NeoplasmsCoronary Artery DiseaseDiabetes Mellitus, Type 2FemaleGenetic Predisposition to DiseaseHumansPrediction AlgorithmsRisk AssessmentRisk FactorsDeep learningGenome wide association studyMedical history recordPolygenic risk scoreSingle nucleotide polymorphism

Identifiers

PMID40963070
PMCPMC13219203

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.