Abstract 4369799: AI-enhanced ECG for diastolic dysfunction: development, validation and prognosis across five international cohorts

L Libor Pastika (Imperial College London, London, United Kingdom) B Boroumand Zeidaabadi (Imperial College London, London, United Kingdom) K Konstantinos Patlatzoglou (Imperial College London, London, United Kingdom) G Gul Rukh Khattak (Imperial College London, London, United Kingdom) J Joseph Barker H Hesham Aggour (Imperial College London, London, United Kingdom) A Ahmed El-Medany (Imperial College London, London, United Kingdom) B Brett Bernstein (KINGS COLLEGE LONDON, London, United Kingdom) J Jack Wu (KINGS COLLEGE LONDON, London, United Kingdom) K Kevin O Gallagher (KINGS COLLEGE LONDON, London, United Kingdom) A Ajay Shah (KINGS COLLEGE LONDON, London, United Kingdom) S Sandhi Maria Barreto (Universidade Federal Minas Gerais, Belo Horizonte, Brazil) M Murilo Foppa (HCPA, PortoAlegre, Brazil) G Gabriela Paixao (Universidade Federal de Minas Gerai, Belo Horizonte, Brazil) S Sadia Khan (Chelsea and Westminster NHS Foundation Trust, London, United Kingdom) L Luisa Brant (Universidade Federal de Minas Gerai, Belo Horizonte, Brazil) D Daniel Kramer (Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States) J Jonathan Waks (Beth Israel Deaconess Medical Cente, Newton Center, Massachusetts, United States) N Nicholas Peters (Imperial College London, London, United Kingdom) A Antonio Luiz Ribeiro (UFMG, Belo Horizonte, Brazil) A Arunashis Sau (Imperial College London, London, United Kingdom) F Fu Siong Ng

Abstract

Background: Evaluation of left ventricular diastolic function is integral to diagnosing heart failure with preserved ejection fraction (HFpEF), but echocardiography is resource-intensive and not always available, leading to delayed detection. We developed an AI-enhanced ECG (AI-ECG) model to detect echocardiography-determined diastolic dysfunction (DD). Methods: The AI-Risk Estimator for DD (AIRE-DD) is a residual neural network with a discrete-time survival loss function. It was trained on 89,100 ECG-echocardiography (ECG–TTE) pairs from Beth Israel Deaconess Medical Center (BIDMC) and externally validated in four cohorts: King’s College Hospital (KCH; n=1 635), CODE (Brazil; n=882,212), ELSA-Brasil (n=13,739) and UK Biobank (UKB; n = 65 610). Results: In the BIDMC holdout set (n = 35,760 ECG–TTE pairs), AIRE-DD detected increased LV filling pressures with an AUC of 0.883 (95 % CI 0.874–0.891), sensitivity 0.780, specificity 0.822, PPV 0.564 and NPV 0.927. AIRE-DD also detected grades of diastolic dysfunction with AUCs of 0.792 (≥ grade I), 0.882 (≥ grade II) and 0.906 (grade III). For incident DD prediction in BIDMC participants without baseline DD and LVEF ≥ 50 %, AIRE-DD achieved a C-index of 0.751 (95 % CI 0.719–0.791). In KCH, AIRE-DD identified clinician-confirmed HFpEF with an AUC of 0.850 (0.809–0.887). In BIDMC, increased filling pressures predicted by AIRE-DD stratified incident outcomes at least as well as echocardiography (age- and sex-adjusted hazard ratios [HRs]: mortality 2.09 vs 1.98; atherosclerotic cardiovascular disease 2.02 vs 1.70; atrial fibrillation 2.12 vs 1.79; heart failure 2.24 vs 2.40; chronic kidney disease 1.93 vs 1.70). Across BIDMC, CODE, ELSA-Brasil and UKB, AIRE-DD-predicted increased filling pressures were associated with age- and sex-adjusted HRs for all-cause mortality of 2.05 (1.87–2.26), 2.83 (2.75–2.92), 4.38 (3.46–5.52) and 1.67 (1.33–2.09), respectively. Explainability analyses showed that AIRE-DD predictions correlated with broad QRS morphology, T-wave inversion/flattening and poor precordial R-wave progression, and were associated with echocardiographic metrics of impaired relaxation, chamber enlargement and myocardial remodelling. Conclusion: AIRE-DD provides a non-invasive, scalable method for detection and prediction of diastolic dysfunction and stratification of mortality risk, supporting its potential as a first-line screening tool to prioritise patients for confirmatory imaging and early intervention.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (22)

L

Libor Pastika

Imperial College London, London, United Kingdom

B

Boroumand Zeidaabadi

Imperial College London, London, United Kingdom

K

Konstantinos Patlatzoglou

Imperial College London, London, United Kingdom

G

Gul Rukh Khattak

Imperial College London, London, United Kingdom

J

Joseph Barker

H

Hesham Aggour

Imperial College London, London, United Kingdom

A

Ahmed El-Medany

Imperial College London, London, United Kingdom

B

Brett Bernstein

KINGS COLLEGE LONDON, London, United Kingdom

J

Jack Wu

KINGS COLLEGE LONDON, London, United Kingdom

K

Kevin O Gallagher

KINGS COLLEGE LONDON, London, United Kingdom

A

Ajay Shah

KINGS COLLEGE LONDON, London, United Kingdom

S

Sandhi Maria Barreto

Universidade Federal Minas Gerais, Belo Horizonte, Brazil

M

Murilo Foppa

HCPA, PortoAlegre, Brazil

G

Gabriela Paixao

Universidade Federal de Minas Gerai, Belo Horizonte, Brazil

S

Sadia Khan

Chelsea and Westminster NHS Foundation Trust, London, United Kingdom

L

Luisa Brant

Universidade Federal de Minas Gerai, Belo Horizonte, Brazil

D

Daniel Kramer

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

J

Jonathan Waks

Beth Israel Deaconess Medical Cente, Newton Center, Massachusetts, United States

N

Nicholas Peters

Imperial College London, London, United Kingdom

A

Antonio Luiz Ribeiro

UFMG, Belo Horizonte, Brazil

A

Arunashis Sau

Imperial College London, London, United Kingdom

F

Fu Siong Ng