Deep learning analysis of electrocardiogram for risk prediction of drug-induced arrhythmias and diagnosis of long QT syndrome.


Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
07 10 2021
Historique:
received: 11 04 2021
revised: 13 06 2021
accepted: 12 08 2021
pubmed: 2 9 2021
medline: 25 2 2023
entrez: 1 9 2021
Statut: ppublish

Résumé

Congenital long-QT syndromes (cLQTS) or drug-induced long-QT syndromes (diLQTS) can cause torsade de pointes (TdP), a life-threatening ventricular arrhythmia. The current strategy for the identification of drugs at the high risk of TdP relies on measuring the QT interval corrected for heart rate (QTc) on the electrocardiogram (ECG). However, QTc has a low positive predictive value. We used convolutional neural network (CNN) models to quantify ECG alterations induced by sotalol, an IKr blocker associated with TdP, aiming to provide new tools (CNN models) to enhance the prediction of drug-induced TdP (diTdP) and diagnosis of cLQTS. Tested CNN models used single or multiple 10-s recordings/patient using 8 leads or single leads in various cohorts: 1029 healthy subjects before and after sotalol intake (n = 14 135 ECGs); 487 cLQTS patients (n = 1083 ECGs: 560 type 1, 456 type 2, 67 type 3); and 48 patients with diTdP (n = 1105 ECGs, with 147 obtained within 48 h of a diTdP episode). CNN models outperformed models using QTc to identify exposure to sotalol [area under the receiver operating characteristic curve (ROC-AUC) = 0.98 vs. 0.72, P ≤ 0.001]. CNN models had higher ROC-AUC using multiple vs. single 10-s ECG (P ≤ 0.001). Performances were comparable for 8-lead vs. single-lead models. CNN models predicting sotalol exposure also accurately detected the presence and type of cLQTS vs. healthy controls, particularly for cLQT2 (AUC-ROC = 0.9) and were greatest shortly after a diTdP event and declining over time (P ≤ 0.001), after controlling for QTc and intake of culprit drugs. ECG segment analysis identified the J-Tpeak interval as the best discriminator of sotalol intake. CNN models applied to ECGs outperform QTc measurements to identify exposure to drugs altering the QT interval, congenital LQTS, and are greatest shortly after a diTdP episode.

Identifiants

pubmed: 34468739
pii: 6361017
doi: 10.1093/eurheartj/ehab588
doi:

Substances chimiques

Pharmaceutical Preparations 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3948-3961

Commentaires et corrections

Type : CommentIn

Informations de copyright

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2021. For permissions, please email: journals.permissions@oup.com.

Auteurs

Edi Prifti (E)

IRD, Sorbonne University, UMMISCO, 32 Avenue Henri Varagnat, Bondy 93143, France.
Sorbonne University, INSERM, NutriOmics, 91 Boulevard de l'Hopital, Paris 75013, France.

Ahmad Fall (A)

IRD, Sorbonne University, UMMISCO, 32 Avenue Henri Varagnat, Bondy 93143, France.

Giovanni Davogustto (G)

Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.

Alfredo Pulini (A)

IRD, Sorbonne University, UMMISCO, 32 Avenue Henri Varagnat, Bondy 93143, France.
Faculty of Medicine, Université de Paris, Paris, France.

Isabelle Denjoy (I)

CNMR Maladies Cardiaques Héréditaires Rares, Hôpital Bichat, Paris, France.

Christian Funck-Brentano (C)

Clinical Investigation Center Paris-Est, CIC-1901, INSERM, UNICO-GRECO Cardio-Oncology Program, Department of Pharmacology, Pitié-Salpêtrière University Hospital, Sorbonne Universite, 47 Boulevard de l'Hopital, Paris 7513, France.

Yasmin Khan (Y)

Banook Group, Nancy, France.

Alexandre Durand-Salmon (A)

Banook Group, Nancy, France.

Fabio Badilini (F)

AMPS LLC, New York, USA.

Quinn S Wells (QS)

Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA.

Antoine Leenhardt (A)

CNMR Maladies Cardiaques Héréditaires Rares, Hôpital Bichat, Paris, France.

Jean-Daniel Zucker (JD)

IRD, Sorbonne University, UMMISCO, 32 Avenue Henri Varagnat, Bondy 93143, France.
Sorbonne University, INSERM, NutriOmics, 91 Boulevard de l'Hopital, Paris 75013, France.

Dan M Roden (DM)

Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.

Fabrice Extramiana (F)

CNMR Maladies Cardiaques Héréditaires Rares, Hôpital Bichat, Paris, France.

Joe-Elie Salem (JE)

Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Clinical Investigation Center Paris-Est, CIC-1901, INSERM, UNICO-GRECO Cardio-Oncology Program, Department of Pharmacology, Pitié-Salpêtrière University Hospital, Sorbonne Universite, 47 Boulevard de l'Hopital, Paris 7513, France.
Department of Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA.

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