Evidence map›Paper›PMID 41602938›Full record

ArticleDigital health

Benchmarking survival machine learning models for 10-year cardiovascular disease risk prediction using large-scale electronic health records.

Tianyi Liu, Andrew Krentz, Lei Lu, Yanzhong Wang, Vasa Curcin

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Article in Digital health. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

5 authors.

Tianyi LiuSchool of Life Course & Population Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0002-0912-7652
Andrew KrentzSchool of Life Course & Population Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0003-4169-0469
Lei LuSchool of Life Course & Population Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0001-9139-8955
Yanzhong WangSchool of Life Course & Population Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0002-0768-1676
Vasa CurcinSchool of Life Course & Population Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0002-8308-2886

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To evaluate the performance of machine learning (ML)-based survival models for 10-year cardiovascular disease (CVD) risk prediction using large-scale electronic health records (EHRs). The study benchmarks these models against the QRISK3 score and conventional Cox proportional hazards (CoxPH) models currently used in UK primary prevention, with the aim of assessing their potential to capture complex risk patterns beyond traditional approaches. Methods: This study utilized individual-level data from the CPRD Aurum, covering 40 million UK primary care records from 2011 to 2021. A total of 469,496 patients aged 40-85 was analysed. Predictor variables were selected based on QRISK3 definitions, with additional phenotyping for comorbidities and pre-stratified risk scores. ML models, including deep neural networks (e.g., DeepSurv and DeepHit) and ensemble survival models (e.g., random survival forest [RSF] and gradient boosting), were developed for CVD risk prediction. Model performance was assessed using calibration and discrimination metrics, with 'spatial external validation' conducted using a London-held dataset. Results: A total of 849,651 records were analysed, including 117,421 for 'spatial validation' and 732,230 for development. QRISK3 scores effectively differentiated CVD patients, particularly among females, showing stronger predictive performance. Ensemble methods and neural networks outperformed CoxPH models, with RSF achieving the best discrimination and calibration: AUROC values of 0.738 (95% CI: 0.723-0.752) for males and 0.778 (95% CI: 0.762-0.793) for females, with Brier scores of 0.088 and 0.055. Conclusion: ML models enhance CVD risk prediction, outperforming conventional approaches in calibration and discrimination. Integrating pre-stratified risk scores further improves performance, highlighting the value of augmenting tools like QRISK.

Indexed as

Cardiovascular diseaseselectronic health recordsmachine learningrisk predictionsurvival analysis

Identifiers

PMID41602938
PMCPMC12833136

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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.