Simes R John, Marschner Ian C, Hunt David, Colquhoun David, Sullivan David, Stewart Ralph A H, Hague Wendy, Keech Anthony, Thompson Peter, White Harvey, Shaw John, Tonkin Andrew
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Australia.
Circulation. 2002 Mar 12;105(10):1162-9. doi: 10.1161/hc1002.105136.
The Long-Term Intervention with Pravastatin in Ischemic Disease (LIPID) trial showed that pravastatin significantly reduced mortality and coronary heart disease (CHD) events in 9014 patients with known CHD and total cholesterol 4.0 to 7.0 mmol/L at baseline. Secondary objectives included assessment of CHD event reduction according to lipid levels.
We investigated the relationships of baseline and on-study lipids with subsequent CHD events in separate Cox models. Treatment effect on CHD event reduction was examined by baseline lipids and after adjustment for on-study lipid levels. Baseline lipids were significant predictors of CHD events. The adjusted relative risk per mmol/L (on placebo) was 1.24 (P=0.004) for total cholesterol, 1.28 (P=0.002) for low-density lipoprotein cholesterol, and 0.52 (P=0.004) for high-density lipoprotein cholesterol. Apolipoproteins A1 and B were strong predictors (each P=0.001). Pravastatin reduced the risk of the composite outcome of fatal CHD or nonfatal myocardial infarction by 24% (95% confidence interval [CI], 15% to 32%) and the expanded end point of fatal CHD, nonfatal myocardial infarction, unstable angina, or coronary revascularization by 17% (95% CI, 10% to 24%). Similar relative effects were observed for different categories of baseline lipids. The proportion of treatment effect explained by on-study lipid levels was 67% (95% CI, 27% to 106%) for the composite and 97% (95% CI, 49% to 145%) for the expanded end point. The most important lipids associated with event reduction were apolipoprotein B, low-density lipoprotein cholesterol, and the combination of total and high-density lipoprotein cholesterol.
Changes in lipid levels can explain all or most of the observed benefit of pravastatin. Some treatment effect may also be mediated through nonlipid changes.
普伐他汀长期干预缺血性疾病(LIPID)试验表明,普伐他汀可显著降低9014例基线时已知患有冠心病且总胆固醇水平在4.0至7.0 mmol/L之间的患者的死亡率和冠心病(CHD)事件。次要目标包括根据血脂水平评估冠心病事件的减少情况。
我们在单独的Cox模型中研究了基线血脂和研究期间血脂与随后冠心病事件之间的关系。通过基线血脂并在调整研究期间血脂水平后,检验了治疗对冠心病事件减少的效果。基线血脂是冠心病事件的重要预测指标。每mmol/L(安慰剂组)的调整相对风险,总胆固醇为1.24(P = 0.004),低密度脂蛋白胆固醇为1.28(P = 0.002),高密度脂蛋白胆固醇为0.52(P = 0.004)。载脂蛋白A1和B是强预测指标(均P = 0.001)。普伐他汀使致命性冠心病或非致命性心肌梗死的复合结局风险降低了24%(95%置信区间[CI],15%至32%),使致命性冠心病、非致命性心肌梗死、不稳定型心绞痛或冠状动脉血运重建的扩展终点风险降低了17%(95%CI,10%至24%)。对于不同类别的基线血脂,观察到了相似的相对效果。研究期间血脂水平所解释的治疗效果比例,复合结局为67%(95%CI,27%至106%),扩展终点为97%(95%CI,49%至145%)。与事件减少相关的最重要血脂是载脂蛋白B、低密度脂蛋白胆固醇以及总胆固醇与高密度脂蛋白胆固醇的组合。
血脂水平的变化可以解释普伐他汀所观察到的全部或大部分益处。一些治疗效果也可能通过非血脂变化介导。