Development and validation of a machine learning model to predict myocardial blood flow and clinical outcomes from patients' electrocardiograms.

artificial intelligence coronary artery disease electrocardiography machine learning major adverse cardiovascular events myocardial blood flow positron emission tomography

Journal

Cell reports. Medicine
ISSN: 2666-3791
Titre abrégé: Cell Rep Med
Pays: United States
ID NLM: 101766894

Informations de publication

Date de publication:
18 Sep 2024
Historique:
received: 09 05 2024
revised: 24 07 2024
accepted: 30 08 2024
medline: 27 9 2024
pubmed: 27 9 2024
entrez: 26 9 2024
Statut: aheadofprint

Résumé

We develop a machine learning (ML) model using electrocardiography (ECG) to predict myocardial blood flow reserve (MFR) and assess its prognostic value for major adverse cardiovascular events (MACEs). Using 3,639 ECG-positron emission tomography (PET) and 17,649 ECG-single-photon emission computed tomography (SPECT) data pairs, the ML model is trained with a swarm intelligence approach and support vector regression (SVR). The model achieves a receiver-operator curve (ROC) area under the curve (AUC) of 0.83, with a sensitivity and specificity of 0.75. An ECG-MFR value below 2 is significantly associated with MACE, with hazard ratios (HRs) of 3.85 and 3.70 in the discovery and validation phases, respectively. The model's C-statistic is 0.76, with a net reclassification improvement (NRI) of 0.35. Validated in an independent cohort, the ML model using ECG data offers superior MACE prediction compared to baseline clinical models, highlighting its potential for risk stratification in patients with coronary artery disease (CAD) using the accessible 12-lead ECG.

Identifiants

pubmed: 39326409
pii: S2666-3791(24)00476-2
doi: 10.1016/j.xcrm.2024.101746
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101746

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Fares Alahdab (F)

Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA; Departments of Biomedical Informatics, Biostatistics, Epidemiology, and Cardiology, University of Missouri, Columbia, MO.

Maliazurina Binti Saad (MB)

Department of Imaging Physics, Division of Diagnostic Imaging, MD Anderson Cancer Center, Houston, TX, USA.

Ahmed Ibrahim Ahmed (AI)

Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA.

Qasem Al Tashi (Q)

Department of Imaging Physics, Division of Diagnostic Imaging, MD Anderson Cancer Center, Houston, TX, USA.

Muhammad Aminu (M)

Department of Imaging Physics, Division of Diagnostic Imaging, MD Anderson Cancer Center, Houston, TX, USA.

Yushui Han (Y)

Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA.

Jonathan B Moody (JB)

INVIA Medical Imaging Solutions, 3025 Boardwalk Dr., Suite 200, Ann Arbor, MI 48108, USA.

Venkatesh L Murthy (VL)

Division of Cardiovascular Medicine, Department of Medicine, and Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA.

Jia Wu (J)

Department of Imaging Physics, Division of Diagnostic Imaging, MD Anderson Cancer Center, Houston, TX, USA. Electronic address: //jwu11@mdanderson.org.

Mouaz H Al-Mallah (MH)

Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA. Electronic address: mal-mallah@houstonmethodist.org.

Classifications MeSH