Cardiovascular benefits of statin plus ezetimibe combination therapy versus statin monotherapy in acute coronary syndrome: a meta-analysis of randomized controlled trials

Author:

de Oliveira Almeida Gustavo1,Balieiro Caroline2,Bertoli Edmundo Damiani3,Moreira Maria Eduarda Liporaci1,Silva Ana Laura Soares1,Minucci Bárbara Silvestre1,Zapparoli Isabella1,Maluf Marcela Silva1,Carvalho Henrique Champs Porfírio1,dos Santos Borges Rafael4,Pasqualotto Eric5,Nienkötter Thiago3,Alves Vinícius6,Guida Camila Mota7

Affiliation:

1. Department of Medicine, Federal University of Triângulo Mineiro, Uberaba

2. Department of Medicine, State University of Amazonas, Manaus

3. Department of Medicine, University of South Santa Catarina, Palhoça

4. Department of Medicine, Federal University of Minas Gerais, Belo Horizonte

5. Department of Medicine, Federal University of Santa Catarina, Florianópolis

6. Department of Medicine, University of São Paulo

7. Division of Cardiology, Department of Cardiology, Dante Pazzanese Institute of Cardiology, São Paulo, Brazil

Abstract

Background The efficacy of adding ezetimibe to statin therapy for event reduction in patients with acute coronary syndromes (ACS) remains a topic of ongoing debate. Methods We performed a systematic review and meta-analysis of randomized controlled trials (RCTs) comparing ezetimibe plus statin versus statin monotherapy in patients with ACS. We searched PubMed, Embase, and Cochrane for eligible trials. The random-effects model was used to calculate the risk ratios with 95% confidence intervals (CIs). Statistical analyses were performed using RStudio version 4.2.3 (RStudio, PBC). Results Six RCTs comprising 20 574 patients with ACS were included, of whom 10 259 (49.9%) were prescribed ezetimibe plus statin. The patient population had an average age of 63.8 years, and 75.1% were male. Compared with statin monotherapy, ezetimibe plus statin significantly reduced major adverse cardiovascular events (MACE) (risk ratio 0.93; 95% CI 0.90–0.97; P < 0.01) and nonfatal myocardial infarction (risk ratio 0.88; 95% CI 0.81–0.95; P < 0.01). There was no significant difference between groups for revascularization (risk ratio 0.94; 95% CI 0.90–1.00; P = 0.03), all-cause mortality (risk ratio 0.87; 95% CI 0.63–1.21; P = 0.42), or unstable angina (risk ratio 1.05; 95% CI 0.86–1.27; P = 0.64). Conclusion In this meta-analysis of patients with ACS, the combination of ezetimibe plus statin was associated with a reduction in MACE and nonfatal myocardial infarction, compared with statin monotherapy.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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