Abstract 4366487: Artificial Intelligence-Enabled Electrocardiogram for the Detection of Elevated Filling Pressure in Hypertrophic Cardiomyopathy and Cardiac Amyloidosis

R Robin Van Lerberghe (UZ Leuven, Leuven, Belgium) B Bert Vandenberk (UZ Leuven, Leuven, Belgium) J Johanna Jacobs (Mayo Clinic and UZ Leuven, Leuven, Belgium) V Veerle Servaes (UZ Leuven, Leuven, Belgium) T Tomas Robyns (Department of Cardiovascular Sciences (R.P., R.D.B., J.D.P., Y.B., B.D., P.S., T.K., T.R., R.W., G.C.), Katholieke Universiteit Leuven, Belgium.) L Lucas Van Aelst (UZ Leuven, Leuven, Belgium) K Kathryn Mangold (Mayo Clinic, Rochester, Minnesota, United States) Z Zachi Attia (Mayo Clinic, Rochester, Minnesota, United States) J Jae Oh (Mayo Clinic, Rochester, Minnesota, United States) M Martha Grogan (Department of Cardiovascular Medicine (M.G., O.F.A.E., M.C.B., J.J.M.), Mayo Clinic, Rochester, MN.) P Paul Friedman (Mayo Clinic, Rochester, Minnesota, United States) J Joerg Herrmann (Mayo Clinic, Rochester, Minnesota, United States) S Stefan Janssens (University Hospitals Leuven, Leuven, Belgium)

Abstract

Introduction: Diastolic dysfunction is a hallmark of heart failure with preserved ejection fraction, yet echocardiographic grading is challenging in patients with hypertrophic or amyloid cardiomyopathies due to variable structural and functional remodeling. Consequently, there is a need for additional diagnostic tools to identify patients at increased risk of diastolic dysfunction and enhanced filling pressure. Research Question: What is the accuracy of an artificial intelligence (AI)-enabled electrocardiogram (ECG) model to predict diastolic dysfunction in hypertrophic and amyloid cardiomyopathy? Methods: We included patients with diverse phenotypes of hypertrophic cardiomyopathy (HCM) and cardiac amyloidosis and validated Mayo Clinic's AI-enabled ECG model to grade diastolic function (normal: grade 0/1; abnormal: grade 2/3). Echocardiographic analysis of systolic (LVEF) and diastolic function was performed within 14 days of ECG recording. Diastolic function was graded based on E/e’ (>14), left atrial volume index (>34 mL/m2), pulmonary venous atrial reversal flow duration (≥30 ms), and peak tricuspid regurgitation velocity (>2.8 m/s). Filling pressure was considered increased if ≥3 parameters were abnormal, inconclusive if 2 were abnomal, and normal if ≥3 were normal. Echocardiograms with severe mitral regurgitation were excluded. Results: We identified and matched 840 ECGs from non-obstructive HCM patients (n=125, age 58±19y, 70% male), 145 ECGs from obstructive HCM patients (n=29, age 56±18y, 66% male), 225 ECGs from apical HCM patients (n=33, age 66±14y, 61% male), and 382 ECGs from cardiac amyloidosis patients (n=49, age 70±13y, 57% male). The AI-enabled ECG model predicted diastolic dysfunction with an accuracy of 65% (non-obstructive HCM), 67% (obstructive HCM), 65% (apical HCM), and 75% (cardiac amyloidosis), with sensitivities of 94% and 97% for obstructive HCM and cardiac amyloidosis, respectively, and high positive and negative predictive values for cardiac amyloidosis. Systolic dysfunction (LVEF≤40%) was more common in cardiac amyloidosis (29%) than in all HCM patients (5%). Conclusion: The AI-enabled ECG model demonstrates moderate accuracy but high sensitivity for detecting diastolic dysfunction and increased filling pressure, especially in obstructive HCM and cardiac amyloidosis. The AI-enabled ECG is a useful, widely scalable, and low cost tool to identify patients at increased risk for diastolic dysfunction.

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 (13)

R

Robin Van Lerberghe

UZ Leuven, Leuven, Belgium

B

Bert Vandenberk

UZ Leuven, Leuven, Belgium

J

Johanna Jacobs

Mayo Clinic and UZ Leuven, Leuven, Belgium

V

Veerle Servaes

UZ Leuven, Leuven, Belgium

T

Tomas Robyns

Department of Cardiovascular Sciences (R.P., R.D.B., J.D.P., Y.B., B.D., P.S., T.K., T.R., R.W., G.C.), Katholieke Universiteit Leuven, Belgium.

L

Lucas Van Aelst

UZ Leuven, Leuven, Belgium

K

Kathryn Mangold

Mayo Clinic, Rochester, Minnesota, United States

Z

Zachi Attia

Mayo Clinic, Rochester, Minnesota, United States

J

Jae Oh

Mayo Clinic, Rochester, Minnesota, United States

M

Martha Grogan

Department of Cardiovascular Medicine (M.G., O.F.A.E., M.C.B., J.J.M.), Mayo Clinic, Rochester, MN.

P

Paul Friedman

Mayo Clinic, Rochester, Minnesota, United States

J

Joerg Herrmann

Mayo Clinic, Rochester, Minnesota, United States

S

Stefan Janssens

University Hospitals Leuven, Leuven, Belgium