Abstract 4368498: Artificial Intelligence-enhanced Electrocardiography Sex-Discordance is Associated with Cardiovascular Events and Risk Factors in Women: from the ELSA-Brasil study

L Lidyane Camelo (Universidade Federal de Minas Gerai, Belo Horizonte, Brazil) A Arunashis Sau (Imperial College London, London, United Kingdom) S Sandhi Barreto (Universidade Federal de Minas Gerai, Belo Horizonte, Brazil) L Luana Giatti (Universidade Federal de Minas Gerai, Belo Horizonte, Brazil) C Clara Oliveira (Universidade Federal de Minas Gerai, Belo Horizonte, Brazil) G Gabriela Paixao (Universidade Federal de Minas Gerai, Belo Horizonte, Brazil) J Joseph Barker L Libor Pastika (Imperial College London, London, United Kingdom) K Konstantinos Patlatzoglou (Imperial College London, London, United Kingdom) B Boroumand Zeidaabadi (Imperial College London, London, United Kingdom) M Marcelo Pinto Filho (UFMG, Nova Lima, Brazil) A Antonio Luiz Ribeiro (UFMG, Belo Horizonte, Brazil) F Fu Ng (Imperial College London, London, United Kingdom) L Luisa Brant (Universidade Federal de Minas Gerai, Belo Horizonte, Brazil)

Abstract

Introduction: Using sex as a binary variable may oversimplify the spectrum of inter-individual variability in sex-related cardiovascular (CV) risk. Artificial intelligence–enhanced electrocardiography (AI-ECG) models can accurately predict sex in populations from Europe and the US, in whom sex misclassification is associated with adverse CV outcomes in women, but not in men. It is unknown whether AI-ECG accurately identifies sex or predicts CV risk in diverse populations. Objective: To validate the AI-ECG sex-discordance score in the diverse ELSA-Brasil cohort and assess whether an increased sex-discordance score is associated with 5-year CV events. Methods: In the community-based ELSA-Brasil study, we validated the AI-ECG model that predicts sex as a continuous variable. The outcome was mortality or hospitalizations due to myocardial infarction, stroke, heart failure, or revascularization. The AI-ECG sex-discordance score (absolute difference between the AI-predicted sex and self-reported sex, encoded as 0 for men and 1 for women) was analyzed as a standardized continuous variable and quartiles. Association between the sex-discordance score and outcome was assessed using sex-specific multivariable Fine and Gray models accounting for the competing risk of death, adjusted for age, race, education, smoking, physical activity, excessive alcohol consumption, body mass index, hypertension, diabetes, dyslipidemia, and prevalent CV disease. We also evaluated the association of sex-discordance scores with CV risk factors using robust linear regression M-estimator and 95% efficiency. Results: In 13,730 participants from the ELSA-Brasil study (mean age=52±9, 54% women, 45% Black), AI-ECG accurately identified sex (AUC:0.963, 95%CI:0.960-0.965). In women, each 1-SD increase in sex-discordance score was borderline associated with higher risk of CV outcomes (HR 1.19; 95%CI: 1.00–1.42; p=0.057), but no association was seen in men (HR 1.07; 95%CI: 0.80–1.41; p=0.649). Women in the highest quartile of sex-discordance had significantly higher risk compared to the lowest quartile (HR 1.42; 95%CI: 1.02–1.98; p=0.036), but not men. In women, overweight/obesity, smoking, hypertension, and diabetes were associated with higher sex-discordance scores. Conclusions: AI-ECG accurately identifies sex in a diverse population, in whom a high sex-discordance score identifies women with higher CV risk, who might benefit from targeted CV prevention.

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 (14)

L

Lidyane Camelo

Universidade Federal de Minas Gerai, Belo Horizonte, Brazil

A

Arunashis Sau

Imperial College London, London, United Kingdom

S

Sandhi Barreto

Universidade Federal de Minas Gerai, Belo Horizonte, Brazil

L

Luana Giatti

Universidade Federal de Minas Gerai, Belo Horizonte, Brazil

C

Clara Oliveira

Universidade Federal de Minas Gerai, Belo Horizonte, Brazil

G

Gabriela Paixao

Universidade Federal de Minas Gerai, Belo Horizonte, Brazil

J

Joseph Barker

L

Libor Pastika

Imperial College London, London, United Kingdom

K

Konstantinos Patlatzoglou

Imperial College London, London, United Kingdom

B

Boroumand Zeidaabadi

Imperial College London, London, United Kingdom

M

Marcelo Pinto Filho

UFMG, Nova Lima, Brazil

A

Antonio Luiz Ribeiro

UFMG, Belo Horizonte, Brazil

F

Fu Ng

Imperial College London, London, United Kingdom

L

Luisa Brant

Universidade Federal de Minas Gerai, Belo Horizonte, Brazil