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

被引:46
|
作者
Tunon, Jose [1 ,2 ]
Steg, Philippe Gabriel [3 ,4 ]
Bhatt, Deepak L. [5 ]
Bittner, Vera A. [6 ]
Diaz, Rafael [7 ,8 ]
Goodman, Shaun G. [9 ]
Jukema, J. Wouter [10 ]
Kim, Yong-Un [11 ]
Li, Qian H. [12 ]
Mueller, Christian [13 ,14 ]
Parkhomenko, Alexander [15 ]
Pordy, Robert [12 ]
Sritara, Piyamitr [16 ]
Szarek, Michael [17 ]
White, Harvey D. [18 ]
Zeiher, Andreas M. [19 ]
Schwartz, Gregory G. [20 ]
机构
[1] Univ Autonoma Madrid, Fdn Jimenez Diaz, Div Cardiol, Ave Reyes Catolicos 2, Madrid 28040, Spain
[2] CIBER CV, Ave Reyes Catolicos 2, Madrid 28040, Spain
[3] Univ Paris, Dept Cardiol, Hop Bichat, AP HP,FACT,INSERM,U1148, Paris, France
[4] Royal Brompton Hosp, Imperial Coll, Natl Heart & Lung Inst, London, England
[5] Brigham & Womens Hosp, Dept Med, 75 Francis St, Boston, MA 02115 USA
[6] Univ Alabama Birmingham, Div Cardiovasc Dis, Birmingham, AL 35294 USA
[7] Inst Cardiovasc Rosario, Cardiol Dept, Estudios Clin Latinoamer, Rosario, Argentina
[8] Univ Alberta, Canadian VIGOUR Ctr, Edmonton, AB, Canada
[9] Univ Toronto, Div Cardiol, St Michaels Hosp, Toronto, ON, Canada
[10] Leiden Univ, Dept Cardiol, Med Ctr, Leiden, Netherlands
[11] Sanofi, R&D Clin Dev, Paris, France
[12] Regeneron Pharmaceut, Clin Sci Cardiovasc & Metab Therapeut, Tarrytown, NY USA
[13] Univ Basel, Univ Hosp Basel, Cardiovasc Res Inst Basel CRIB, Basel, Switzerland
[14] Univ Basel, Dept Cardiol, Univ Hosp Basel, Basel, Switzerland
[15] Inst Cardiol, Kiev, Ukraine
[16] Ramathibodi Hosp, Dept Med, Bangkok, Thailand
[17] State Univ New York, Downstate Sch Publ Hlth, Brooklyn, NY USA
[18] Auckland City Hosp, Green Lane Cardiovasc Serv, Auckland, New Zealand
[19] Goethe Univ, Dept Med 3, Frankfurt, Germany
[20] Univ Colorado, Div Cardiol, Sch Med, Aurora, CO USA
关键词
PCSK9; inhibition; Acute coronary syndrome; Low-density lipoprotein cholesterol; Chronic kidney disease; Glomerular filtration rate; Major adverse cardiovascular events; CHRONIC KIDNEY-DISEASE; ALL-CAUSE; METAANALYSIS; MECHANISMS; MORTALITY; EFFICACY; SAFETY;
D O I
10.1093/eurheartj/ehaa498
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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) <30mL/min/1.73 m(2) was exclusionary. In 18 918 patients, baseline eGFR was 82.8 +/- 17.6 mL/min/1.73 m(2), 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 mUmin/1.73 m(2) (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 m(2).
引用
收藏
页码:4114 / 4123
页数:10
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