Potential effects of icosapent ethyl on cardiovascular outcomes in cigarette smokers: REDUCE-IT smoking

Author:

Miller Michael12ORCID,Bhatt Deepak L3ORCID,Steg Ph Gabriel4ORCID,Brinton Eliot A5ORCID,Jacobson Terry A6ORCID,Jiao Lixia7ORCID,Tardif Jean-Claude8ORCID,Ballantyne Christie M9ORCID,Budoff Matthew10ORCID,Mason R Preston3ORCID

Affiliation:

1. Corporal Michael J. Crescenz Veterans Affairs Medical Center and Hospital, University of , Philadelphia, PA 19104 , USA

2. Pennsylvania , Philadelphia, PA 19104 , USA

3. Department of Medicine, Brigham and Women's Hospital, Harvard Medical School , Boston, MA , USA

4. Department of Medicine, Université Paris-Cité , Paris , France

5. Department of Medicine, Utah Lipid Center , Salt Lake City, UT , USA

6. Department of Medicine, Emory University School of Medicine , Atlanta, GA , USA

7. Amarin Pharma, Inc. , Bridgewater, NJ , USA

8. Department of Medicine, Montreal Heart Institute , Montreal , Canada

9. Department of Medicine, Baylor College of Medicine , Houston, TX , USA

10. Department of Medicine, University of California, Los Angeles , Los Angeles, CA , USA

Abstract

Abstract Aims Cigarette smoking is among the most well-established risk factors for adverse cardiovascular outcomes. We sought to determine whether icosapent ethyl (IPE), a highly purified form of eicosapentaenoic acid with antiatherothrombotic properties, may reduce the excessive risk of cardiovascular disease (CVD) attributable to smoking. Methods and results Reduction of Cardiovascular Events with Icosapent Ethyl Trial (REDUCE-IT) was a multinational, double-blind trial that randomized 8179 statin-treated patients with elevated triglycerides and CV risk to IPE or placebo, with a median follow-up period of 4.9 years. Icosapent ethyl reduced the primary composite endpoint [CV death, non-fatal myocardial infarction (MI), non-fatal stroke, coronary revascularization, or hospitalization for unstable angina] by 25% (P < 0.0001). In the current analyses, the effect of IPE was evaluated in REDUCE-IT using post hoc analyses based on smoking history. Groups were classified as current smokers (n = 1241), former smokers (n = 3672), and never smokers (n = 3264). Compared with placebo, IPE use in combined current and former smokers (n = 4913) was associated with significant reductions in time to the primary composite endpoint {hazard ratio: 0.77 [95% confidence interval (CI): 0.68–0.87]; P < 0.0001} and in total events [rate ratio: 0.71 (95% CI: 0.61–0.82); P < 0.0001]. These benefits remained significant when subdivided into current and former smokers (P = 0.04, P = 0.005), with reductions in the key secondary composite endpoint (P < 0.0001) and in the individual components of CV death or non-fatal MI (P = 0.04, P = 0.01) and fatal or non-fatal MI (P = 0.009, P = 0.01), respectively. Benefits were consistent and significant in non-smokers as well. Overall, there were similar estimated rates of first occurrences of primary CVD endpoints in current smokers (23.8%) and former smokers (23.0%) assigned to IPE compared with never smokers on placebo (25.7%). Conclusion In REDUCE-IT, IPE treatment was associated with a reduced risk of CV events in current and former smokers to levels observed in never smokers. While smoking cessation should always be recommended, these data raise the possibility that IPE treatment may attenuate CV hazards attributable to smoking.

Funder

Amarin Pharma, Inc.

St. Jude Medical

Abbott

Edwards

Daiichi Sankyo Company

Concept Medical

Boehringer Ingelheim

CSL Behring

Ferring Pharmaceuticals

Bayer

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Cardiology and Cardiovascular Medicine

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