Ezetimibe Added to Statin Therapy after Acute Coronary Syndromes

被引:3012
|
作者
Cannon, Christopher P. [1 ,2 ]
Blazing, Michael A. [3 ]
Giugliano, Robert P. [1 ,2 ]
McCagg, Amy [1 ,2 ]
White, Jennifer A. [3 ]
Theroux, Pierre [4 ]
Darius, Harald [5 ]
Lewis, Basil S. [6 ]
Ophuis, Ton Oude [7 ]
Jukema, J. Wouter [8 ]
De Ferrari, Gaetano M. [9 ,10 ]
Ruzyllo, Witold [11 ]
De Lucca, Paul [12 ]
Im, KyungAh [1 ,2 ]
Bohula, Erin A. [1 ,2 ]
Reist, Craig [3 ]
Wiviott, Stephen D. [1 ,2 ]
Tershakovec, Andrew M. [12 ]
Musliner, Thomas A. [12 ]
Braunwald, Eugene [1 ,2 ]
Califf, Robert M. [3 ]
机构
[1] Brigham & Womens Hosp, Thrombolysis Myocardial Infarct TIMI Study Grp, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] DCRI, Durham, NC USA
[4] Montreal Heart Inst, Montreal, PQ H1T 1C8, Canada
[5] Vivantes Neukolln Med Ctr, Berlin, Germany
[6] Lady Davis Carmel Med Ctr, Haifa, Israel
[7] Canisius Wilhelmina Ziekenhuis, Nijmegen, Netherlands
[8] Netherlands Leiden Univ, Med Ctr, Leiden, Netherlands
[9] Fdn IRCCS Policlin San Matteo, Pavia, Italy
[10] Univ Pavia, I-27100 Pavia, Italy
[11] Natl Inst Cardiol, Warsaw, Poland
[12] Merck, Kenilworth, NJ USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2015年 / 372卷 / 25期
关键词
CARDIOVASCULAR OUTCOMES; CHOLESTEROL ABSORPTION; MYOCARDIAL-INFARCTION; PRIMARY PREVENTION; CARDIAC OUTCOMES; CLINICAL-TRIALS; IMPROVE-IT; ATORVASTATIN; EFFICACY; SIMVASTATIN;
D O I
10.1056/NEJMoa1410489
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Statin therapy reduces low-density lipoprotein (LDL) cholesterol levels and the risk of cardiovascular events, but whether the addition of ezetimibe, a nonstatin drug that reduces intestinal cholesterol absorption, can reduce the rate of cardiovascular events further is not known. METHODS We conducted a double-blind, randomized trial involving 18,144 patients who had been hospitalized for an acute coronary syndrome within the preceding 10 days and had LDL cholesterol levels of 50 to 100 mg per deciliter (1.3 to 2.6 mmol per liter) if they were receiving lipid-lowering therapy or 50 to 125 mg per deciliter (1.3 to 3.2 mmol per liter) if they were not receiving lipid-lowering therapy. The combination of simvastatin (40 mg) and ezetimibe (10 mg) (simvastatin-ezetimibe) was compared with simvastatin (40 mg) and placebo (simvastatin monotherapy). The primary end point was a composite of cardiovascular death, nonfatal myocardial infarction, unstable angina requiring rehospitalization, coronary revascularization (>= 30 days after randomization), or nonfatal stroke. The median follow-up was 6 years. RESULTS The median time-weighted average LDL cholesterol level during the study was 53.7 mg per deciliter (1.4 mmol per liter) in the simvastatin-ezetimibe group, as compared with 69.5 mg per deciliter (1.8 mmol per liter) in the simvastatin-monotherapy group (P< 0.001). The Kaplan-Meier event rate for the primary end point at 7 years was 32.7% in the simvastatin-ezetimibe group, as compared with 34.7% in the simvastatin-monotherapy group (absolute risk difference, 2.0 percentage points; hazard ratio, 0.936; 95% confidence interval, 0.89 to 0.99; P = 0.016). Rates of pre-specified muscle, gallbladder, and hepatic adverse effects and cancer were similar in the two groups. CONCLUSIONS When added to statin therapy, ezetimibe resulted in incremental lowering of LDL cholesterol levels and improved cardiovascular outcomes. Moreover, lowering LDL cholesterol to levels below previous targets provided additional benefit.
引用
收藏
页码:2387 / 2397
页数:11
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