Effect of lowering LDL cholesterol substantially below currently recommended levels in patients with coronary heart disease and diabetes - The treating to new targets (TNT) study

被引:391
作者
Shepherd, James
Breazna, Andrei
Barter, Philip
LaRosa, John
Carmena, Rafael
Grundy, Scott
Deedwania, Prakash
Waters, David
Fruchart, Jean-Charles
Haffner, Steven
Hsia, Judith
机构
[1] Univ Glasgow, Dept Vasc Biochem, Glasgow, Lanark, Scotland
[2] Univ Sydney, Dept Med, Heart Res Inst, Sydney, NSW 2006, Australia
[3] Univ Valencia, Clin Univ Hosp, Dept Endocrinol, Valencia, Spain
[4] Univ Calif San Francisco, Div Cardiol, Vet Affairs Cent Calif Hlth Care, Sch Med, San Francisco, CA 94143 USA
[5] Inst Pasteur, Lipoprot & Atherosclerosis Res Unit, INSERM, F-59019 Lille, France
[6] Univ Texas, Hlth Sci Ctr, Dept Med, San Antonio, TX 78284 USA
[7] George Washington Univ, Med Ctr, Div Cardiol, Washington, DC 20037 USA
[8] Pfizer, Biometr Dept, New York, NY USA
[9] SUNY Hlth Sci Ctr, Suny Downstate Med Ctr, Brooklyn, NY 11203 USA
[10] Univ Texas, SW Med Ctr, Ctr Human Nutr, Dept Clin Nutr, Dallas, TX 75230 USA
[11] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75230 USA
[12] Univ Calif San Francisco, Sch Med, San Francisco Gen Hosp, Div Cardiol, San Francisco, CA 94143 USA
关键词
D O I
10.2337/dc05-2465
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE- The Treating to New Targets study showed that intensive lipid-lowering therapy with atorvastatin 80 mg/day provides significant clinical benefit beyond that afforded by atorvastatin 10 mg/day in patients with stable coronary heart disease (CHD). The objective of our study was to investigate whether similar benefits of high-dose intensive atorvastatin therapy can be achieved in patients with CHD and diabetes. RESEARCH DESIGN AND METHODS- A total of 1,501 patients with diabetes and CHD, with LDL cholesterol levels of < 130 mg/dI, were randomized to double-blind therapy with either atorvastatin 10 (n = 753) or 80 (n = 748) mg/day. Patients were followed for a median of 4.9 years. The primary end point was the time to first major cardiovascular event, defined as death from CHD, nonfatal non-procedure-related myocardial infarction, resuscitated cardiac arrest, or fatal or nonfatal stroke. RESULTS- End-of-treatment mean LDL cholesterol levels were 98.6 mg/dl with atorvastatin 10 mg and 77.0 mg/dl with atorvastatin 80 mg. A primary event occurred in 135 patients (17.9%) receiving atorvastatin 10 mg, compared with 103 patients (13.8%) receiving atorvastatin 80 mg (hazard ratio 0.75 [95% Cl 0.58-0.97], P = 0.026). Significant differences between the groups in favor of atorvastatin 80 mg were also observed for time to cerebrovascular event (0.69 [0.48-0.98], P = 0.037) and any cardiovascular event (0.85 [0.73-1.00], P = 0.044). There were no significant differences between the treatment groups in the rates of treatment-related adverse events and persistent elevations in liver enzymes.
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收藏
页码:1220 / 1226
页数:7
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