Rosuvastatin to Prevent Vascular Events in Men and Women with Elevated C-Reactive Protein

被引:5078
作者
Ridker, Paul M. [1 ,2 ]
Danielson, Eleanor [1 ]
Fonseca, Francisco A. H. [3 ]
Genest, Jacques [4 ]
Gotto, Antonio M., Jr. [5 ]
Kastelein, John J. P. [6 ]
Koenig, Wolfgang [7 ]
Libby, Peter [2 ]
Lorenzatti, Alberto J. [8 ]
MacFadyen, Jean G. [1 ]
Nordestgaard, Borge G. [9 ]
Shepherd, James [10 ]
Willerson, James T. [11 ]
Glynn, Robert J. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Ctr Cardiovasc Dis Prevent, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Cardiovasc Med, Boston, MA 02215 USA
[3] Univ Fed Sao Paulo, Sao Paulo, Brazil
[4] McGill Univ, Ctr Hlth, Montreal, PQ, Canada
[5] Cornell Univ, Weill Cornell Med Coll, New York, NY 10021 USA
[6] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, NL-1105 AZ Amsterdam, Netherlands
[7] Univ Ulm, Med Ctr, Ulm, Germany
[8] Hosp Cordoba, Cordoba, Argentina
[9] Copenhagen Univ Hosp, Herlev Hosp, Herlev, Denmark
[10] Univ Glasgow, Glasgow, Lanark, Scotland
[11] St Lukes Episcopal Hosp, Texas Heart Inst, Houston, TX 77030 USA
关键词
D O I
10.1056/NEJMoa0807646
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Increased levels of the inflammatory biomarker high-sensitivity C-reactive protein predict cardiovascular events. Since statins lower levels of high-sensitivity C-reactive protein as well as cholesterol, we hypothesized that people with elevated high-sensitivity C-reactive protein levels but without hyperlipidemia might benefit from statin treatment. Methods: We randomly assigned 17,802 apparently healthy men and women with low-density lipoprotein (LDL) cholesterol levels of less than 130 mg per deciliter (3.4 mmol per liter) and high-sensitivity C-reactive protein levels of 2.0 mg per liter or higher to rosuvastatin, 20 mg daily, or placebo and followed them for the occurrence of the combined primary end point of myocardial infarction, stroke, arterial revascularization, hospitalization for unstable angina, or death from cardiovascular causes. Results: The trial was stopped after a median follow-up of 1.9 years (maximum, 5.0). Rosuvastatin reduced LDL cholesterol levels by 50% and high-sensitivity C-reactive protein levels by 37%. The rates of the primary end point were 0.77 and 1.36 per 100 person-years of follow-up in the rosuvastatin and placebo groups, respectively (hazard ratio for rosuvastatin, 0.56; 95% confidence interval [CI], 0.46 to 0.69; P<0.00001), with corresponding rates of 0.17 and 0.37 for myocardial infarction (hazard ratio, 0.46; 95% CI, 0.30 to 0.70; P=0.0002), 0.18 and 0.34 for stroke (hazard ratio, 0.52; 95% CI, 0.34 to 0.79; P=0.002), 0.41 and 0.77 for revascularization or unstable angina (hazard ratio, 0.53; 95% CI, 0.40 to 0.70; P<0.00001), 0.45 and 0.85 for the combined end point of myocardial infarction, stroke, or death from cardiovascular causes (hazard ratio, 0.53; 95% CI, 0.40 to 0.69; P<0.00001), and 1.00 and 1.25 for death from any cause (hazard ratio, 0.80; 95% CI, 0.67 to 0.97; P=0.02). Consistent effects were observed in all subgroups evaluated. The rosuvastatin group did not have a significant increase in myopathy or cancer but did have a higher incidence of physician-reported diabetes. Conclusions: In this trial of apparently healthy persons without hyperlipidemia but with elevated high-sensitivity C-reactive protein levels, rosuvastatin significantly reduced the incidence of major cardiovascular events. (ClinicalTrials.gov number, NCT00239681.).
引用
收藏
页码:2195 / 2207
页数:13
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