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Deep learning to predict left ventricular hypertrophy from the electrocardiogram.

Hafiz Naderi1,2, Thomas Kaplan1, Stefan van Duijvenboden1,3

  • 1William Harvey Research Institute, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK.

Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology
|January 27, 2026
PubMed
Summary
This summary is machine-generated.

A deep learning model accurately predicts left ventricular hypertrophy (LVH) from ECGs, outperforming previous methods. Further development with diverse datasets is needed to ensure broad applicability.

Keywords:
Deep learningElectrocardiogramLeft ventricular hypertrophyMachine learning

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Area of Science:

  • Cardiology
  • Artificial Intelligence
  • Medical Imaging

Background:

  • Left ventricular hypertrophy (LVH) is a significant predictor of cardiovascular disease.
  • Previous supervised machine learning models for LVH classification using ECG and clinical data achieved an AUROC of 0.85 but required external validation.
  • External validation is crucial for assessing the generalizability of predictive models.

Purpose of the Study:

  • To develop a deep learning (DL) model for improved classification of cardiac magnetic resonance (CMR)-derived LVH.
  • To externally evaluate the DL model's performance in the Study of Health in Pomerania (SHIP) cohort.
  • To assess the feasibility of DL-based ECG screening tools for LVH prediction.

Main Methods:

  • A fully convolutional network DL model was developed using 12-lead ECGs and clinical variables from 48,835 UK Biobank participants.
  • The model predicted indexed left ventricular mass (iLVM), with logistic regression used for recalibration.
  • Performance was evaluated using area under the receiving operating curve (AUROC) in training, validation, and test sets, and externally in the SHIP cohort.

Main Results:

  • The DL model achieved an AUROC of 0.97 in the UK Biobank cohort, significantly outperforming previous methods.
  • The QRS complex and ventricular rate on ECG were identified as key predictors of LVH.
  • The DL model demonstrated modest generalizability to the SHIP cohort (AUROC 0.78), with variations attributed to clinical profiles, ECG acquisition, and CMR labeling.

Conclusions:

  • Scalable DL-based screening tools for LVH prediction from ECG are feasible.
  • Further model development using larger, more diverse datasets is necessary to enhance generalizability.
  • Differences in cohort characteristics and data acquisition impact model performance across different populations.