Sacks F M, Tonkin A M, Shepherd J, Braunwald E, Cobbe S, Hawkins C M, Keech A, Packard C, Simes J, Byington R, Furberg C D
Brigham and Women's Hospital, Harvard Medical School Boston, MA 02115, USA.
Circulation. 2000 Oct 17;102(16):1893-900. doi: 10.1161/01.cir.102.16.1893.
Previous trials have had insufficient numbers of coronary events to address definitively the effect of lipid-modifying therapy on coronary heart disease in subgroups of patients with varying baseline characteristics.
The data from 3 large randomized trials with pravastatin 40 mg were pooled and analyzed with the use of a prospectively defined protocol. Included were 19 768 patients, 102 559 person-years of follow-up, 2194 primary end points (coronary death or nonfatal myocardial infarction), and 3717 expanded end points (primary end point, CABG, or PTCA). Pravastatin significantly reduced relative risk in younger (<65 years) and older (>/=65 years) patients, men and women, smokers and nonsmokers, and patients with or without diabetes or hypertension. The relative effect was smaller, but absolute risk reduction was similar in patients with hypertension compared with those without hypertension. Relative risk reduction was significant in predefined categories of baseline lipid concentrations. Tests for interaction were not significant between relative risk reduction and baseline total cholesterol (5% to 95% range 177 to 297 mg/dL, 4.6 to 7.7 mmol/L), HDL cholesterol (27 to 58 mg/dL, 0.7 to 1.5 mmol/L), and triglyceride (74 to 302 mg/dL, 0.8 to 3.4 mmol/L) concentrations, analyzed as continuous variables. However, for LDL cholesterol, the probability values for interaction were 0.068 for the prespecified primary end point and 0.019 for the expanded end point. Relative risk reduction was similar throughout most of the baseline LDL cholesterol range (125 to 212 mg/dL, 3.2 to 5.5 mmol/L) with the possible exception of the lowest quintile of CARE/LIPID (<125 mg/dL) (relative risk reduction 5%, 95% CI 19% to -12%).
Pravastatin treatment is effective in reducing coronary heart disease events in patients with high or low risk factor status and across a wide range of pretreatment lipid concentrations.
既往试验中冠状动脉事件数量不足,无法明确脂质修饰治疗对具有不同基线特征的患者亚组中冠心病的影响。
汇总了3项使用40mg普伐他汀的大型随机试验的数据,并采用前瞻性定义的方案进行分析。纳入19768例患者,随访102559人年,2194个主要终点(冠心病死亡或非致死性心肌梗死),3717个扩展终点(主要终点、冠状动脉搭桥术或经皮冠状动脉腔内血管成形术)。普伐他汀显著降低了年轻(<65岁)和年长(≥65岁)患者、男性和女性、吸烟者和非吸烟者以及有或无糖尿病或高血压患者的相对风险。与无高血压患者相比,高血压患者的相对效应较小,但绝对风险降低相似。在预先定义的基线血脂浓度类别中,相对风险降低显著。作为连续变量分析时,相对风险降低与基线总胆固醇(5%至95%范围为177至297mg/dL,4.6至7.7mmol/L)、高密度脂蛋白胆固醇(27至58mg/dL,0.7至1.5mmol/L)和甘油三酯(74至302mg/dL,0.8至3.4mmol/L)浓度之间的交互作用检验无显著性。然而,对于低密度脂蛋白胆固醇,预先设定的主要终点的交互作用概率值为0.068,扩展终点的为0.019。在大部分基线低密度脂蛋白胆固醇范围(125至212mg/dL,3.2至5.5mmol/L)内,相对风险降低相似,可能除外CARE/LIPID研究中最低五分位数(<125mg/dL)(相对风险降低5%,95%CI为19%至 -12%)。
普伐他汀治疗在降低高风险或低风险因素状态患者以及广泛的治疗前血脂浓度范围内的冠心病事件方面有效。