Robins S J, Collins D, Wittes J T, Papademetriou V, Deedwania P C, Schaefer E J, McNamara J R, Kashyap M L, Hershman J M, Wexler L F, Rubins H B
Department of Medicine, Boston University School of Medicine, 88 E Newton St, Boston, MA 02118, USA.
JAMA. 2001 Mar 28;285(12):1585-91. doi: 10.1001/jama.285.12.1585.
A low plasma level of high-density lipoprotein cholesterol (HDL-C) is a major risk factor for coronary heart disease (CHD). A secondary prevention study, the Veterans Affairs High-Density Lipoprotein Intervention Trial (VA-HIT), demonstrated that CHD events were significantly reduced during a median follow-up of 5.1 years by treating patients with the fibric acid derivative gemfibrozil when the predominant lipid abnormality was low HDL-C.
To determine if the reduction in major CHD events with gemfibrozil in VA-HIT could be attributed to changes in major plasma lipid levels.
Multicenter, randomized, double-blind, placebo-controlled trial conducted from September 1991 to August 1998.
The Department of Veterans Affairs Cooperative Studies Program, in which 20 VA medical centers were participating sites.
A total of 2531 men with a history of CHD who had low HDL-C levels (mean, 32 mg/dL [0.83 mmol/L] ) and low low-density lipoprotein cholesterol (LDL-C) levels (mean, 111 mg/dL [2.88 mmol/L]).
Participants were randomly assigned to receive gemfibrozil, 1200 mg/d (n = 1264), or matching placebo (n = 1267).
Relation of lipid levels at baseline and averaged during the first 18 months of gemfibrozil treatment with the combined incidence of nonfatal myocardial infarction and CHD death.
Concentrations of HDL-C were inversely related to CHD events. Multivariable Cox proportional hazards analysis showed that CHD events were reduced by 11% with gemfibrozil for every 5-mg/dL (0.13-mmol/L) increase in HDL-C (P =.02). Events were reduced even further with gemfibrozil beyond that explained by increases in HDL-C values, particularly in the second through fourth quintiles of HDL-C values during treatment. During gemfibrozil treatment, only the increase in HDL-C significantly predicted a lower risk of CHD events; by multivariable analysis, neither triglyceride nor LDL-C levels at baseline or during the trial predicted CHD events.
Concentrations of HDL-C achieved with gemfibrozil treatment predicted a significant reduction in CHD events in patients with low HDL-C levels. However, the change in HDL-C levels only partially explained the beneficial effect of gemfibrozil.
血浆高密度脂蛋白胆固醇(HDL-C)水平低是冠心病(CHD)的主要危险因素。一项二级预防研究,即退伍军人事务部高密度脂蛋白干预试验(VA-HIT)表明,在主要脂质异常为HDL-C水平低的患者中,使用纤维酸衍生物吉非贝齐进行治疗,在中位随访5.1年期间,冠心病事件显著减少。
确定VA-HIT中吉非贝齐使主要冠心病事件减少是否可归因于主要血脂水平的变化。
1991年9月至1998年8月进行的多中心、随机、双盲、安慰剂对照试验。
退伍军人事务部合作研究项目,20个退伍军人事务医疗中心为参与地点。
共有2531名有冠心病病史的男性,其HDL-C水平低(平均32mg/dL[0.83mmol/L])且低密度脂蛋白胆固醇(LDL-C)水平低(平均111mg/dL[2.88mmol/L])。
参与者被随机分配接受吉非贝齐,1200mg/d(n=1264),或匹配的安慰剂(n=1267)。
基线时以及吉非贝齐治疗的前18个月期间平均血脂水平与非致命性心肌梗死和冠心病死亡的合并发生率之间的关系。
HDL-C浓度与冠心病事件呈负相关。多变量Cox比例风险分析显示,HDL-C每增加5mg/dL(0.13mmol/L),吉非贝齐使冠心病事件减少11%(P=0.02)。吉非贝齐使事件减少的幅度甚至超过了HDL-C值升高所能解释的范围,特别是在治疗期间HDL-C值的第二至第四五分位数时。在吉非贝齐治疗期间,只有HDL-C的升高显著预测了较低的冠心病事件风险;通过多变量分析,基线时或试验期间的甘油三酯和LDL-C水平均未预测冠心病事件。
吉非贝齐治疗所达到的HDL-C浓度预测了HDL-C水平低的患者冠心病事件显著减少。然而,HDL-C水平的变化仅部分解释了吉非贝齐的有益作用。