Evidence map›Paper›PMID 40309320›Full record

ArticleFrontiers in digital health2025

Deep conditional generative model for personalization of 12-lead electrocardiograms and cardiovascular risk prediction.

Yuling Sang, Abhirup Banerjee, Marcel Beetz, Vicente Grau

Abstract read
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Article in Frontiers in digital health, 2025. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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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

4 authors.

Yuling SangCentre for Computational Biology, Duke-NUS Medical School, Singapore, Singapore.
Abhirup BanerjeeInstitute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, United Kingdom.
Marcel BeetzInstitute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, United Kingdom.
Vicente GrauInstitute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: 12-lead electrocardiograms (ECGs) are a cornerstone for diagnosing and monitoring cardiovascular diseases (CVDs). They play a key role in detecting abnormalities such as arrhythmias and myocardial infarction, enabling early intervention and risk stratification. However, traditional analysis relies heavily on manual interpretation, which is time-consuming and expertise-dependent. Moreover, existing machine learning models often lack personalization, as they fail to integrate subject-specific anatomical and demographic information. Advances in deep generative models offer an opportunity to overcome these challenges by synthesizing personalized ECGs and extracting clinically relevant features for improved risk assessment. Methods: We propose a conditional Variational Autoencoder (cVAE) framework to generate realistic, subject-specific 12-lead ECGs by incorporating demographic metadata, anatomical heart features, and ECG electrodes' positions as conditioning factors. This allows for physiologically consistent and personalized ECG synthesis. Furthermore, we introduce a revised Cox proportional-hazards regression model that utilizes the latent embeddings learned by the cVAE to predict future CVD risk. This approach not only enhances the interpretability of ECG-derived risk factors but also demonstrates the potential of deep generative models in personalized cardiac assessment. Results: Our model is trained and validated on the UK Biobank dataset and Conclusion: This work marks a significant advancement in ECG analysis by providing a conditional VAE framework that not only improves ECG generation but also enriches our understanding of the relationship between ECG patterns and subject-specific information. Importantly, our approach enables clinically significant information to be extracted from 12-lead ECGs, providing valuable insights for predicting future CVD risks.

Indexed as

cardiac MRIcardiovascular diseasecardiovascular risk predictionECG electrodesECG generationvariational autoencoder

Identifiers

PMID40309320
PMCPMC12040958

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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.