Wenger Nanette K, Lewis Sandra J, Herrington David M, Bittner Vera, Welty Francine K
Division of Cardiology, Emory University School of Medicine, Atlanta, Georgia 30303, USA.
Ann Intern Med. 2007 Jul 3;147(1):1-9. doi: 10.7326/0003-4819-147-1-200707030-00002.
Increased life expectancy is associated with an increase in the burden of chronic cardiovascular disease.
To assess the efficacy and safety of high-dose atorvastatin in patients 65 years of age or older.
A prespecified secondary analysis of the Treating to New Targets study, a randomized, double-blind clinical trial.
256 sites in 14 countries participating in the Treating to New Targets study.
10,001 patients (3809 patients > or =65 years of age) with coronary heart disease (CHD) and low-density lipoprotein cholesterol levels less than 3.4 mmol/L (<130 mg/dL).
Patients were randomly assigned to receive atorvastatin, 10 or 80 mg/d.
The primary end point was the occurrence of a first major cardiovascular event (death from CHD, nonfatal non-procedure-related myocardial infarction, resuscitated cardiac arrest, or fatal or nonfatal stroke).
In patients 65 years of age or older, absolute risk was reduced by 2.3% and relative risk by 19% for major cardiovascular events in favor of the high-dose atorvastatin group (hazard ratio, 0.81 [95% CI, 0.67 to 0.98]; P = 0.032). Among the components of the composite outcome, the mortality rates from CHD, nonfatal non-procedure-related myocardial infarction, and fatal or nonfatal stroke (ischemic, embolic, hemorrhagic, or unknown origin) were all lower in older patients who received high-dose atorvastatin, although the difference was not statistically significant for each individual component. The improved clinical outcome in patients 65 years of age or older was not associated with persistent elevations in creatine kinase levels.
Because the study was a secondary analysis, the findings should be interpreted within the context of the main study results.
The analysis suggests that additional clinical benefit can be achieved by treating older patients with CHD more aggressively to reduce low-density lipoprotein cholesterol levels to less than 2.6 mmol/L (<100 mg/dL). The findings support the use of intensive low-density lipoprotein cholesterol-lowering therapy in high-risk older persons with established cardiovascular disease. Click here for related information on atorvastatin.
预期寿命的延长与慢性心血管疾病负担的增加相关。
评估大剂量阿托伐他汀在65岁及以上患者中的疗效和安全性。
对“治疗达新目标”研究进行预先设定的二次分析,这是一项随机、双盲临床试验。
14个国家的256个研究点参与了“治疗达新目标”研究。
10001例冠心病(CHD)患者,低密度脂蛋白胆固醇水平低于3.4 mmol/L(<130 mg/dL)(3809例患者年龄≥65岁)。
患者被随机分配接受阿托伐他汀,10 mg/d或80 mg/d。
主要终点是首次发生的重大心血管事件(CHD死亡、非致死性非手术相关心肌梗死、心脏骤停复苏、或致死性或非致死性卒中)。
在65岁及以上患者中,大剂量阿托伐他汀组的重大心血管事件绝对风险降低了2.3%,相对风险降低了19%(风险比,0.81 [95% CI,0.67至0.98];P = 0.032)。在综合结局的各组成部分中,接受大剂量阿托伐他汀治疗的老年患者中,CHD死亡率、非致死性非手术相关心肌梗死以及致死性或非致死性卒中(缺血性、栓塞性、出血性或不明原因)的发生率均较低,尽管各单个组成部分的差异无统计学意义。65岁及以上患者临床结局的改善与肌酸激酶水平持续升高无关。
由于该研究是二次分析,研究结果应结合主要研究结果进行解释。
该分析表明,对老年CHD患者更积极地治疗,将低密度脂蛋白胆固醇水平降至低于2.6 mmol/L(<100 mg/dL),可获得额外的临床益处。研究结果支持在已确诊心血管疾病的高危老年人群中使用强化降低低密度脂蛋白胆固醇治疗。点击此处获取阿托伐他汀的相关信息。