Prediction of incident atrial fibrillation using deep learning, clinical models and polygenic scores.
Atrial fibrillation
deep learning
electrocardiogram
polygenic scores
Journal
European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263
Informations de publication
Date de publication:
01 Sep 2024
01 Sep 2024
Historique:
received:
15
07
2024
revised:
08
08
2024
accepted:
21
08
2024
medline:
1
9
2024
pubmed:
1
9
2024
entrez:
1
9
2024
Statut:
aheadofprint
Résumé
Deep learning applied to electrocardiograms (ECG-AI) is an emerging approach for predicting atrial fibrillation or flutter (AF). This study introduces an ECG-AI model developed and tested at a tertiary cardiac centre, comparing its performance with clinical and AF polygenic scores (PGS). ECG in sinus rhythm from the Montreal Heart Institute were analysed, excluding those from patients with preexisting AF. The primary outcome was incident AF at 5 years. An ECG-AI model was developed by splitting patients into non-overlapping datasets: 70% for training, 10% for validation, and 20% for testing. Performance of ECG-AI, clinical models and PGS was assessed in the test dataset. The ECG-AI model was externally validated in the Medical Information Mart for Intensive Care-IV (MIMIC-IV) hospital dataset. A total of 669,782 ECGs from 145,323 patients were included. Mean age was 61±15 years, and 58% were male. The primary outcome was observed in 15% of patients and the ECG-AI model showed an area under the receiver operating characteristic curve (AUC) of 0.78. In time-to-event analysis including the first ECG, ECG-AI inference of high risk identified 26% of the population with a 4.3-fold increased risk of incident AF (95% confidence interval 4.02-4.57). In a subgroup analysis of 2,301 patients, ECG-AI outperformed CHARGE-AF (AUC=0.62) and PGS (AUC=0.59). Adding PGS and CHARGE-AF to ECG-AI improved goodness-of-fit (likelihood ratio test p<0.001), with minimal changes to the AUC (0.76-0.77). In the external validation cohort (mean age 59±18 years, 47% male, median follow-up 1.1 year) ECG-AI model performance= remained consistent (AUC=0.77). ECG-AI provides an accurate tool to predict new-onset AF in a tertiary cardiac centre, surpassing clinical and polygenic scores.
Sections du résumé
BACKGROUND AND AIMS
OBJECTIVE
Deep learning applied to electrocardiograms (ECG-AI) is an emerging approach for predicting atrial fibrillation or flutter (AF). This study introduces an ECG-AI model developed and tested at a tertiary cardiac centre, comparing its performance with clinical and AF polygenic scores (PGS).
METHODS
METHODS
ECG in sinus rhythm from the Montreal Heart Institute were analysed, excluding those from patients with preexisting AF. The primary outcome was incident AF at 5 years. An ECG-AI model was developed by splitting patients into non-overlapping datasets: 70% for training, 10% for validation, and 20% for testing. Performance of ECG-AI, clinical models and PGS was assessed in the test dataset. The ECG-AI model was externally validated in the Medical Information Mart for Intensive Care-IV (MIMIC-IV) hospital dataset.
RESULTS
RESULTS
A total of 669,782 ECGs from 145,323 patients were included. Mean age was 61±15 years, and 58% were male. The primary outcome was observed in 15% of patients and the ECG-AI model showed an area under the receiver operating characteristic curve (AUC) of 0.78. In time-to-event analysis including the first ECG, ECG-AI inference of high risk identified 26% of the population with a 4.3-fold increased risk of incident AF (95% confidence interval 4.02-4.57). In a subgroup analysis of 2,301 patients, ECG-AI outperformed CHARGE-AF (AUC=0.62) and PGS (AUC=0.59). Adding PGS and CHARGE-AF to ECG-AI improved goodness-of-fit (likelihood ratio test p<0.001), with minimal changes to the AUC (0.76-0.77). In the external validation cohort (mean age 59±18 years, 47% male, median follow-up 1.1 year) ECG-AI model performance= remained consistent (AUC=0.77).
CONCLUSIONS
CONCLUSIONS
ECG-AI provides an accurate tool to predict new-onset AF in a tertiary cardiac centre, surpassing clinical and polygenic scores.
Identifiants
pubmed: 39217446
pii: 7740534
doi: 10.1093/eurheartj/ehae595
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.