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American Heart Association

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Final ID: MP1490

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

Abstract Body (Do not enter title and authors here): 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.
  • Lee, Pei-lun  ( Jacobi Medical Center , Bronx , New York , United States )
  • Romero Acero, Laura  ( Cardiac Care and Vascular Medicine , Bronx , New York , United States )
  • Nanna, Md, Facc, Michele  ( Albert Einstein Coll of Med , Bronx , New York , United States )
  • Rios, Saul  ( Montefiore Medical Center , Bronx , New York , United States )
  • Thankachen, Jincy  ( Jacobi Medical Center , Bronx , New York , United States )
  • Damluji, Abdulla  ( Cleveland Clinic , Cleveland , Ohio , United States )
  • Nanna, Michael  ( Yale School of Medicine , New Haven , Connecticut , United States )
  • Chi, Kuan Yu  ( Jacobi Medical Center , Bronx , New York , United States )
  • Hsieh, Rebecca  ( Danbury Hospital , Danbury , Connecticut , United States )
  • Osabutey, Anita  ( Jacobi Medical Center , Bronx , New York , United States )
  • Mangalesh, Sridhar  ( Albert Einstein College of Medicine , Bronx , New York , United States )
  • Hu, Jiun-ruey  ( cedar-sinai medical center , Los Angeles , California , United States )
  • Chang, Yu  ( National Cheng Kung University Hospital , Tainan City , Tainan , Taiwan )
  • Ezenna, Chidubem  ( UMass- Baystate Medical Center , Springfield , Massachusetts , United States )
  • Faillace, Robert  ( Jacobi Medical Center , Bronx , New York , United States )
  • Author Disclosures:
    Pei-Lun Lee: DO NOT have relevant financial relationships | Laura Romero Acero: No Answer | Michele Nanna, MD, FACC: DO NOT have relevant financial relationships | Saul Rios: DO NOT have relevant financial relationships | Jincy Thankachen: DO NOT have relevant financial relationships | Abdulla Damluji: DO NOT have relevant financial relationships | Michael Nanna: DO have relevant financial relationships ; Consultant:HeartFlow, Inc.:Active (exists now) ; Consultant:Merck:Active (exists now) ; Consultant:Novo Nordisk:Active (exists now) | Kuan Yu Chi: DO NOT have relevant financial relationships | Rebecca Hsieh: DO NOT have relevant financial relationships | Anita Osabutey: DO NOT have relevant financial relationships | Sridhar Mangalesh: DO NOT have relevant financial relationships | Jiun-Ruey Hu: DO NOT have relevant financial relationships | Yu Chang: No Answer | Chidubem Ezenna: DO NOT have relevant financial relationships | Robert Faillace: No Answer
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:

Targeteing Lipid-Associated Cardiovascular Disease Risk

Sunday, 11/09/2025 , 09:15AM - 10:30AM

Moderated Digital Poster Session

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Glucagon-like Peptide-1 Receptor Agonists for the Primary Prevention of Major Adverse Cardiac Events in Drug-naïve Type 2 Diabetes: A Propensity-score Analysis

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Early GLP-1 Receptor Agonist Initiation Reduces Major Cardiac and Renal Events in Older Adults with Type 2 Diabetes Without Prior Cardiovascular or Renal Disease: A Target Trial Emulation

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