Effect of alirocumab on major adverse cardiovascular events according to renal function in patients with a recent acute coronary syndrome: prespecified analysis from the ODYSSEY OUTCOMES randomized clinical trial

Author:

Tuñón José1,Steg Philippe Gabriel23,Bhatt Deepak L4ORCID,Bittner Vera A5ORCID,Díaz Rafael6,Goodman Shaun G7ORCID,Jukema J Wouter8,Kim Yong-Un9ORCID,Li Qian H10,Mueller Christian11ORCID,Parkhomenko Alexander12,Pordy Robert10ORCID,Sritara Piyamitr13,Szarek Michael14ORCID,White Harvey D15ORCID,Zeiher Andreas M16,Schwartz Gregory G17,

Affiliation:

1. Division of Cardiology, Fundación Jiménez Díaz, Autónoma University, and CIBER CV, Avenida Reyes Católicos 2, 28040 Madrid, Spain

2. Department of Cardiology, Université de Paris, Assistance Publique-Hôpitaux de Paris, Hôpital Bichat, Université de Paris, FACT (French Alliance for Cardiovascular Trials), INSERM U1148, Paris, France

3. National Heart and Lung Institute, Imperial College, Royal Brompton Hospital, London, UK

4. Department of Medicine, Brigham and Women’s Hospital, Boston, MA, USA

5. Division of Cardiovascular Disease, University of Alabama at Birmingham, Birmingham, AL, USA

6. Cardiology Department, Estudios Clínicos Latinoamérica, Instituto Cardiovascular de Rosario, Rosario, Argentina; Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada

7. Division of Cardiology, St. Michael’s Hospital, University of Toronto, Toronto, ON, Canada

8. Department of Cardiology, Leiden University Medical Center, Leiden, the Netherlands

9. R & D clinical Development, Sanofi, Paris, France

10. Clinical Sciences-Cardiovascular & Metabolism Therapeutics, Regeneron Pharmaceuticals, Tarrytown, NY, USA

11. Cardiovascular Research Institute Basel (CRIB) and Department of Cardiology, University Hospital Basel, University of Basel, Switzerland

12. Institute of Cardiology, Kyiv, Ukraine

13. Department of Medicine, Ramathibodi Hospital, Bangkok, Thailand

14. State University of New York, Downstate School of Public Health, Brooklyn, NY, USA

15. Green Lane Cardiovascular Services Auckland City Hospital, Auckland, New Zealand

16. Department of Medicine III, Goethe University, Frankfurt am Main, Germany

17. Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA

Abstract

Abstract Aims Statins reduce cardiovascular risk in patients with acute coronary syndrome (ACS) and normal-to-moderately impaired renal function. It is not known whether proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors provide similar benefit across a range of renal function. We determined whether effects of the PCSK9 inhibitor alirocumab to reduce cardiovascular events and death after ACS are influenced by renal function. Methods and results ODYSSEY OUTCOMES compared alirocumab with placebo in patients with recent ACS and dyslipidaemia despite intensive statin treatment. Estimated glomerular filtration rate (eGFR) <30 mL/min/1.73 m2 was exclusionary. In 18 918 patients, baseline eGFR was 82.8 ± 17.6 mL/min/1.73 m2, and low-density lipoprotein cholesterol (LDL-C) was 92 ± 31 mg/dL. At 36 months, alirocumab decreased LDL-C by 48.5% vs. placebo but did not affect eGFR (P = 0.65). Overall, alirocumab reduced risk of the primary outcome (coronary heart disease death, non-fatal myocardial infarction, ischaemic stroke, or unstable angina requiring hospitalization) with fewer deaths. There was no interaction between continuous eGFR and treatment on the primary outcome or death (P = 0.14 and 0.59, respectively). Alirocumab reduced primary outcomes in patients with eGFR ≥90 mL/min/1.73 m2 (n = 7470; hazard ratio 0.784, 95% confidence interval 0.670–0.919; P = 0.003) and 60 to <90 (n = 9326; 0.833, 0.731–0.949; P = 0.006), but not in those with eGFR < 60 (n = 2122; 0.974, 0.805–1.178; P = 0.784). Adverse events other than local injection-site reactions were similar in both groups across all categories of eGFR. Conclusions In patients with recent ACS, alirocumab was associated with fewer cardiovascular events and deaths across the range of renal function studied, with larger relative risk reductions in those with eGFR > 60 mL/min/1.73 m2.

Funder

Sanofi and Regeneron Pharmaceuticals, Inc

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Reference25 articles.

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