Effects of Dalcetrapib in Patients with a Recent Acute Coronary Syndrome

被引:1580
作者
Schwartz, Gregory G. [1 ,16 ]
Olsson, Anders G. [2 ]
Abt, Markus [3 ]
Ballantyne, Christie M. [4 ,5 ]
Barter, Philip J. [6 ]
Brumm, Jochen [3 ]
Chaitman, Bernard R. [7 ]
Holme, Ingar M. [8 ]
Kallend, David [3 ]
Leiter, Lawrence A. [9 ]
Leitersdorf, Eran [10 ]
McMurray, John J. V. [11 ]
Mundl, Hardi [3 ]
Nicholls, Stephen J. [12 ]
Shah, Prediman K. [13 ]
Tardif, Jean-Claude [14 ]
Wright, R. Scott [15 ]
机构
[1] Univ Colorado, Sch Med, Denver, CO USA
[2] Stockholm & Linkoping Univ, Stockholm Heart Ctr, Linkoping, Sweden
[3] F Hoffmann La Roche, Basel, Switzerland
[4] Baylor Coll Med, Houston, TX 77030 USA
[5] Methodist DeBakey Heart & Vasc Ctr, Houston, TX 77030 USA
[6] Heart Res Inst, Sydney, NSW, Australia
[7] St Louis Univ, St Louis, MO 63103 USA
[8] Oslo Univ Hosp, Oslo, Norway
[9] Univ Toronto, St Michaels Hosp, Li Ka Shing Knowledge Inst, Keenan Res Ctr, Toronto, ON M5B 1W8, Canada
[10] Hadassah Hebrew Univ, Med Ctr, Jerusalem, Israel
[11] Univ Glasgow, British Heart Fdn Cardiovasc Res Ctr, Glasgow, Lanark, Scotland
[12] Univ Adelaide, S Australian Hlth & Med Res Inst, Adelaide, SA, Australia
[13] Cedars Sinai Heart Inst, Los Angeles, CA USA
[14] Univ Montreal, Montreal Heart Inst, Montreal, PQ, Canada
[15] Mayo Clin, Rochester, MN USA
[16] Vet Affairs Med Ctr, Denver, CO USA
关键词
HIGH-DENSITY-LIPOPROTEIN; HEART-DISEASE; CARDIOVASCULAR EVENTS; CHOLESTEROL EFFLUX; HDL CHOLESTEROL; STATIN THERAPY; HIGH-RISK; SAFETY; PREVENTION; TRIAL;
D O I
10.1056/NEJMoa1206797
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND In observational analyses, higher levels of high-density lipoprotein (HDL) cholesterol have been associated with a lower risk of coronary heart disease events. However, whether raising HDL cholesterol levels therapeutically reduces cardiovascular risk remains uncertain. Inhibition of cholesteryl ester transfer protein (CETP) raises HDL cholesterol levels and might therefore improve cardiovascular outcomes. METHODS We randomly assigned 15,871 patients who had had a recent acute coronary syndrome to receive the CETP inhibitor dalcetrapib, at a dose of 600 mg daily, or placebo, in addition to the best available evidence-based care. The primary efficacy end point was a composite of death from coronary heart disease, nonfatal myocardial infarction, ischemic stroke, unstable angina, or cardiac arrest with resuscitation. RESULTS At the time of randomization, the mean HDL cholesterol level was 42 mg per deciliter (1.1 mmol per liter), and the mean low-density lipoprotein (LDL) cholesterol level was 76 mg per deciliter (2.0 mmol per liter). Over the course of the trial, HDL cholesterol levels increased from baseline by 4 to 11% in the placebo group and by 31 to 40% in the dalcetrapib group. Dalcetrapib had a minimal effect on LDL cholesterol levels. Patients were followed for a median of 31 months. At a prespecified interim analysis that included 1135 primary end-point events (71% of the projected total number), the independent data and safety monitoring board recommended termination of the trial for futility. As compared with placebo, dalcetrapib did not alter the risk of the primary end point (cumulative event rate, 8.0% and 8.3%, respectively; hazard ratio with dalcetrapib, 1.04; 95% confidence interval, 0.93 to 1.16; P = 0.52) and did not have a significant effect on any component of the primary end point or total mortality. The median C-reactive protein level was 0.2 mg per liter higher and the mean systolic blood pressure was 0.6 mm Hg higher with dalcetrapib as compared with placebo (P<0.001 for both comparisons). CONCLUSIONS In patients who had had a recent acute coronary syndrome, dalcetrapib increased HDL cholesterol levels but did not reduce the risk of recurrent cardiovascular events. (Funded by F. Hoffmann-La Roche; dal-OUTCOMES ClinicalTrials.gov number, NCT00658515.)
引用
收藏
页码:2089 / 2099
页数:11
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