Cholesterol Lowering in Intermediate-Risk Persons without Cardiovascular Disease

Salim Yusuf(Chinese Academy of Medical Sciences & Peking Union Medical College), Jackie Bosch(Chinese Academy of Medical Sciences & Peking Union Medical College), Gilles R. Dagenais(Chinese Academy of Medical Sciences & Peking Union Medical College), Jun Zhu(Chinese Academy of Medical Sciences & Peking Union Medical College), Denis Xavier(Chinese Academy of Medical Sciences & Peking Union Medical College), Lisheng Liu(Chinese Academy of Medical Sciences & Peking Union Medical College), Prem Pais(Chinese Academy of Medical Sciences & Peking Union Medical College), Patricio López‐Jaramillo(Chinese Academy of Medical Sciences & Peking Union Medical College), Lawrence A. Leiter(St. Michael's Hospital), Antonio Dans(Chinese Academy of Medical Sciences & Peking Union Medical College), Álvaro Avezum(Chinese Academy of Medical Sciences & Peking Union Medical College), Leopoldo Soares Piegas(Chinese Academy of Medical Sciences & Peking Union Medical College), Alexander Parkhomenko(Chinese Academy of Medical Sciences & Peking Union Medical College), Katalin Keltai(Semmelweis University), Mátyás Keltai(Semmelweis University), Karen Sliwa(University of Cape Town), Ron J.G. Peters(Chinese Academy of Medical Sciences & Peking Union Medical College), Claes Held(Uppsala University), И Е Чазова(Chinese Academy of Medical Sciences & Peking Union Medical College), Khalid Yusoff(Chinese Academy of Medical Sciences & Peking Union Medical College), Basil S. Lewis(Technion – Israel Institute of Technology), Petr Janský(Chinese Academy of Medical Sciences & Peking Union Medical College), Kamlesh Khunti(Chinese Academy of Medical Sciences & Peking Union Medical College), William D. Toff(University of Leicester), Christopher M. Reid(Chinese Academy of Medical Sciences & Peking Union Medical College), George Varigos(Chinese Academy of Medical Sciences & Peking Union Medical College), Gregorio Sanchez-Vallejo(Chinese Academy of Medical Sciences & Peking Union Medical College), Robert S. McKelvie(Chinese Academy of Medical Sciences & Peking Union Medical College), Janice Pogue(Chinese Academy of Medical Sciences & Peking Union Medical College), Hyejung Jung(Chinese Academy of Medical Sciences & Peking Union Medical College), Peggy Gao(Chinese Academy of Medical Sciences & Peking Union Medical College), Rafael Díaz(Chinese Academy of Medical Sciences & Peking Union Medical College), Eva Lonn(Chinese Academy of Medical Sciences & Peking Union Medical College)
New England Journal of Medicine
April 2, 2016
Cited by 840Open Access
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Abstract

BACKGROUND: Previous trials have shown that the use of statins to lower cholesterol reduces the risk of cardiovascular events among persons without cardiovascular disease. Those trials have involved persons with elevated lipid levels or inflammatory markers and involved mainly white persons. It is unclear whether the benefits of statins can be extended to an intermediate-risk, ethnically diverse population without cardiovascular disease. METHODS: In one comparison from a 2-by-2 factorial trial, we randomly assigned 12,705 participants in 21 countries who did not have cardiovascular disease and were at intermediate risk to receive rosuvastatin at a dose of 10 mg per day or placebo. The first coprimary outcome was the composite of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke, and the second coprimary outcome additionally included revascularization, heart failure, and resuscitated cardiac arrest. The median follow-up was 5.6 years. RESULTS: The overall mean low-density lipoprotein cholesterol level was 26.5% lower in the rosuvastatin group than in the placebo group. The first coprimary outcome occurred in 235 participants (3.7%) in the rosuvastatin group and in 304 participants (4.8%) in the placebo group (hazard ratio, 0.76; 95% confidence interval [CI], 0.64 to 0.91; P=0.002). The results for the second coprimary outcome were consistent with the results for the first (occurring in 277 participants [4.4%] in the rosuvastatin group and in 363 participants [5.7%] in the placebo group; hazard ratio, 0.75; 95% CI, 0.64 to 0.88; P<0.001). The results were also consistent in subgroups defined according to cardiovascular risk at baseline, lipid level, C-reactive protein level, blood pressure, and race or ethnic group. In the rosuvastatin group, there was no excess of diabetes or cancers, but there was an excess of cataract surgery (in 3.8% of the participants, vs. 3.1% in the placebo group; P=0.02) and muscle symptoms (in 5.8% of the participants, vs. 4.7% in the placebo group; P=0.005). CONCLUSIONS: Treatment with rosuvastatin at a dose of 10 mg per day resulted in a significantly lower risk of cardiovascular events than placebo in an intermediate-risk, ethnically diverse population without cardiovascular disease. (Funded by the Canadian Institutes of Health Research and AstraZeneca; HOPE-3 ClinicalTrials.gov number, NCT00468923.).


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