Abstract 4345595: Five-Year Outcomes of Glucagon-Like Peptide-1 Agonists in Obstructive Hypertrophic Cardiomyopathy: A Population-Based Retrospective Study

T Tze Ern Ong (Interfaith Medical Center, Masjid Tanah, Malaysia) M Min Choon Tan (Mayo Clinic Arizona, Phoenix, Arizona, United States) A Aravinthan Vignarajah (Cleveland Clinic Fairview Hospital, Fairview Park, Ohio, United States) D Desmond How Chiat Tan (Melaka-Manipal Medical College, Melaka, Malaysia) O Omar Baqal (Mayo Clinic, Phoenix, Arizona, United States) B Beeletsega Yeneneh (Banner University Medical Group, Phoenix, Arizona, United States) K Kwan Lee (Mayo Clinic Arizona, Scottsdale, Arizona, United States) J Justin Lee (Department for Biochemistry of Plant Interactions, Leibniz Institute of Plant Biochemistry) M Maya Ignaszewski (Northwestern Memorial Hospital, Chicago, Illinois, United States)

Abstract

Background: Glucagon-like peptide-1 (GLP-1) agonists have been shown to improve outcomes across various cardiovascular diseases. However, data regarding the effects of GLP-1 agonists in obstructive hypertrophic cardiomyopathy (HCM) is limited. Objective: This study aimed to evaluate the 5-year outcomes of GLP-1 agonists in patients with HCM. Methods: Using TriNetX Analytics Network, we identified patients aged ≥18 years with a diagnosis of obstructive hypertrophic cardiomyopathy between 1/1/2014 and 1/1/2019. Patients were divided into two groups: those treated with GLP-1 agonists for ≥ 1 year and those who were not. Propensity score matching (PSM) was performed using demographics, cardiac medications, and comorbidities. The study outcomes were 5-year all-cause mortality and cardiac adverse events. Results: A total of 52,978 patients with HCM were identified, including 2,654 (5.0%) patients treated with GLP-1 agonists. After PSM, 2,588 patients in each group were analyzed. Patients on GLP-1 agonists were associated with lower odds of all-cause mortality (5.0% vs. 15.6%, p<0.01), all-cause hospitalization (46.3% vs. 67.8%, p<0.01), acute decompensated heart failure ((9.4% vs. 21.4%, p<0.01), cardiac arrest (3.6% vs. 5.4%, p<0.01), cerebrovascular accidents (9.5% vs. 14.1%, p<0.01), and cardiogenic shock (1.4% vs. 3.6%, p<0.01). Additionally, reduced rates of new ICD implantation (3.5% vs. 7.9%, p<0.01) and septal reduction therapy (1.7% vs. 3.5%, p<0.01) were observed in the GLP-1 agonists group. Conclusion: The use of GLP-1 agonists in HCM was associated with improved cardiovascular outcomes. Future clinical trials are needed to validate these potential benefits.

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 (9)

T

Tze Ern Ong

Interfaith Medical Center, Masjid Tanah, Malaysia

M

Min Choon Tan

Mayo Clinic Arizona, Phoenix, Arizona, United States

A

Aravinthan Vignarajah

Cleveland Clinic Fairview Hospital, Fairview Park, Ohio, United States

D

Desmond How Chiat Tan

Melaka-Manipal Medical College, Melaka, Malaysia

O

Omar Baqal

Mayo Clinic, Phoenix, Arizona, United States

B

Beeletsega Yeneneh

Banner University Medical Group, Phoenix, Arizona, United States

K

Kwan Lee

Mayo Clinic Arizona, Scottsdale, Arizona, United States

J

Justin Lee

Department for Biochemistry of Plant Interactions, Leibniz Institute of Plant Biochemistry

M

Maya Ignaszewski

Northwestern Memorial Hospital, Chicago, Illinois, United States