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首页> 外文期刊>The Lancet >Prevention of coronary and stroke events with atorvastatin in hypertensive patients who have average or lower-than-average cholesterol concentrations, in the Anglo-Scandinavian Cardiac Outcomes Trial--Lipid Lowering Arm (ASCOT-LLA): a multicentre ran
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Prevention of coronary and stroke events with atorvastatin in hypertensive patients who have average or lower-than-average cholesterol concentrations, in the Anglo-Scandinavian Cardiac Outcomes Trial--Lipid Lowering Arm (ASCOT-LLA): a multicentre ran

机译:在盎格鲁-斯堪的纳维亚心脏结果试验-降脂臂(ASCOT-LLA)中,胆固醇水平平均或低于平均水平的高血压患者使用阿托伐他汀预防冠心病和中风事件:多中心

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BACKGROUND: The lowering of cholesterol concentrations in individuals at high risk of cardiovascular disease improves outcome. No study, however, has assessed benefits of cholesterol lowering in the primary prevention of coronary heart disease (CHD) in hypertensive patients who are not conventionally deemed dyslipidaemic. METHODS: Of 19342 hypertensive patients (aged 40-79 years with at least three other cardiovascular risk factors) randomised to one of two antihypertensive regimens in the Anglo-Scandinavian Cardiac Outcomes Trial, 10305 with non-fasting total cholesterol concentrations 6.5 mmol/L or less were randomly assigned additional atorvastatin 10 mg or placebo. These patients formed the lipid-lowering arm of the study. We planned follow-up for an average of 5 years, the primary endpoint being non-fatal myocardial infarction and fatal CHD. Data were analysed by intention to treat. FINDINGS: Treatment was stopped after a median follow-up of 3.3 years. By that time, 100 primary events had occurredin the atorvastatin group compared with 154 events in the placebo group (hazard ratio 0.64 [95% CI 0.50-0.83], p=0.0005). This benefit emerged in the first year of follow-up. There was no significant heterogeneity among prespecified subgroups. Fatal and non-fatal stroke (89 atorvastatin vs 121 placebo, 0.73 [0.56-0.96], p=0.024), total cardiovascular events (389 vs 486, 0.79 [0.69-0.90], p=0.0005), and total coronary events (178 vs 247, 0.71 [0.59-0.86], p=0.0005) were also significantly lowered. There were 185 deaths in the atorvastatin group and 212 in the placebo group (0.87 [0.71-1.06], p=0.16). Atorvastatin lowered total serum cholesterol by about 1.3 mmol/L compared with placebo at 12 months, and by 1.1 mmol/L after 3 years of follow-up. INTERPRETATION: The reductions in major cardiovascular events with atorvastatin are large, given the short follow-up time. These findings may have implications for future lipid-lowering guidelines.
机译:背景:降低心血管疾病高危人群的胆固醇浓度可改善结局。然而,尚无研究评估胆固醇降低在传统上不认为血脂异常的高血压患者一级预防冠心病(CHD)中的益处。方法:在盎格鲁-斯堪的纳维亚心脏结果试验中,将19342例高血压患者(年龄在40-79岁,至少具有其他三个心血管危险因素)随机分配为两种降压方案之一,其中10305例非空腹总胆固醇浓度为6.5 mmol / L或较少者被随机分配额外的阿托伐他汀10 mg或安慰剂。这些患者组成了研究的降脂臂。我们计划平均随访5年,主要终点是非致命性心肌梗塞和致命性冠心病。按意向分析数据。结果:中位随访3.3年后停止治疗。到那时,阿托伐他汀组发生了100例主要事件,而安慰剂组有154例(危险比0.64 [95%CI 0.50-0.83],p = 0.0005)。随访的第一年就产生了这种益处。在预定的亚组之间没有显着的异质性。致命和非致命性中风(89阿托伐他汀vs 121安慰剂,0.73 [0.56-0.96],p = 0.024),总心血管事件(389 vs 486,0.79 [0.69-0.90],p = 0.0005)和总冠状动脉事件( 178 vs 247,0.71 [0.59-0.86],p = 0.0005)也显着降低。阿托伐他汀组有185例死亡,安慰剂组有212例死亡(0.87 [0.71-1.06],p = 0.16)。与安慰剂相比,阿托伐他汀在12个月时降低了总血清胆固醇约1.3 mmol / L,在随访3年后降低了1.1 mmol / L。解释:鉴于随访时间短,阿托伐他汀可减少主要心血管事件的发生。这些发现可能对将来的降脂指南有影响。

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