Abstract 4357689: Upfront Combination of High-Intensity Statin and Ezetimibe Reduces Major Adverse Cardiovascular Events in Acute Myocardial Infarction: A Target-Trial Emulation

P Pei-Lun Lee (Jacobi Medical Center, Bronx, New York, United States) K Kuan Yu Chi (Jacobi Medical Center, Bronx, New York, United States) R Rebecca Hsieh (Danbury Hospital, Danbury, Connecticut, United States) A Anita Osabutey (Jacobi Medical Center, Bronx, New York, United States) S Sridhar Mangalesh (Jacobi Medical Center, Bronx, New York, United States) J Jiun-Ruey Hu (cedar-sinai medical center, Los Angeles, California, United States) Y Yu Chang (State Key Laboratory of Structural Chemistry, Fujian Provincial Key Laboratory of Materials and Techniques toward Hydrogen Energy, Fujian Institute of Research on the Structure of Matter) C Chidubem Ezenna (UMass- Baystate Medical Center, Springfield, Massachusetts, United States) R Robert Faillace L Laura Romero Acero (Cardiac Care and Vascular Medicine, Bronx, New York, United States) M Michele Nanna, MD, FACC (Albert Einstein Coll of Med, Bronx, New York, United States) S Saul Rios (Montefiore Medical Center, Bronx, New York, United States) J Jincy Thankachen (Jacobi Medical Center, Bronx, New York, United States) A Abdulla Damluji (Cleveland Clinic Foundation, Cleveland, Ohio, United States) M Michael Nanna (Yale School of Medicine, New Haven, Connecticut, United States)

Abstract

Background: High-intensity statin treatment has well-established benefits in patients following acute myocardial infarction (AMI). However, the efficacy of combination therapy with ezetimibe in AMI is uncertain. Until recently, ezetimibe was reserved as add-on therapy for secondary lipid lowering post-AMI. Research Question: Does the upfront combination of high-intensity statin treatment with ezetimibe improve cardiovascular outcomes compared with high-intensity statin treatment alone in patients with AMI? Method: We conducted a target-trial emulation using retrospective data from the TriNetX global platform. Adult patients (≥ 18 years) with AMI undergoing revascularization between January 1, 2013, and December 31, 2023, were included. Patients with prior use of high-intensity statins (defined as atorvastatin ≥ 40 mg or rosuvastatin ≥ 20 mg daily), ezetimibe, or previous AMI with revascularization were excluded. Eligible patients were assigned to either combination therapy (high-intensity statin plus ezetimibe) or monotherapy (high-intensity statin alone) within one week of the index AMI. Propensity-score matching (1:1) was used to balance covariates. The primary efficacy outcome was major adverse cardiovascular events (MACE), a composite of all-cause mortality, recurrent AMI, and stroke or transient ischemic attack. Secondary endpoints included individual components of MACE, low-density lipoprotein cholesterol (LDL-C) level, and the rate of achieving LDL-C ≤ 70 mg/dL. Primary safety endpoints were rhabdomyolysis and acute liver failure. Pneumonia was set as a falsification endpoint. Follow-up continued until one year, death, loss to follow-up, or the occurrence of measures. Cox proportional hazards models were used to estimate hazard ratios and 95% confidence interval. Results: A total of 5,416 patients (2,708 per group) were included after propensity-score matching. All covariates were balanced (Table 1) . Combination of high-intensity statin and ezetimibe was associated with a significant reduction in MACE compared with statin alone (Figure 1) , as well as reductions in mortality, AMI, and LDL-C (Table 2) . The rate of achieving LDL-C ≤ 70 mg/dL was superior in the combination group. Safety and falsification endpoints were similar between groups (Table 2) . Conclusion: In patients with AMI undergoing revascularization, upfront combination of a high-intensity statin and ezetimibe was associated with improved cardiovascular outcomes and more effective LDL-C lowering.

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 (15)

P

Pei-Lun Lee

Jacobi Medical Center, Bronx, New York, United States

K

Kuan Yu Chi

Jacobi Medical Center, Bronx, New York, United States

R

Rebecca Hsieh

Danbury Hospital, Danbury, Connecticut, United States

A

Anita Osabutey

Jacobi Medical Center, Bronx, New York, United States

S

Sridhar Mangalesh

Jacobi Medical Center, Bronx, New York, United States

J

Jiun-Ruey Hu

cedar-sinai medical center, Los Angeles, California, United States

Y

Yu Chang

State Key Laboratory of Structural Chemistry, Fujian Provincial Key Laboratory of Materials and Techniques toward Hydrogen Energy, Fujian Institute of Research on the Structure of Matter

C

Chidubem Ezenna

UMass- Baystate Medical Center, Springfield, Massachusetts, United States

R

Robert Faillace

L

Laura Romero Acero

Cardiac Care and Vascular Medicine, Bronx, New York, United States

M

Michele Nanna, MD, FACC

Albert Einstein Coll of Med, Bronx, New York, United States

S

Saul Rios

Montefiore Medical Center, Bronx, New York, United States

J

Jincy Thankachen

Jacobi Medical Center, Bronx, New York, United States

A

Abdulla Damluji

Cleveland Clinic Foundation, Cleveland, Ohio, United States

M

Michael Nanna

Yale School of Medicine, New Haven, Connecticut, United States