Asztalos Bela F, Collins Dorothea, Horvath Katalin V, Bloomfield Hanna E, Robins Sander J, Schaefer Ernst J
Lipid Metabolism Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA 02111, USA.
Metabolism. 2008 Jan;57(1):77-83. doi: 10.1016/j.metabol.2007.08.009.
The significant cardiovascular disease (CVD) event reduction in the Veterans Affairs High-Density Lipoprotein Intervention Trial (VA-HIT) could not be fully explained by the 6% increase in high-density lipoprotein (HDL) cholesterol with the fibrate gemfibrozil. We examined whether measurement of HDL subpopulations provided additional information relative to CVD risk reduction. The HDL subpopulations were characterized by 2-dimensional gel electrophoresis in subjects who were treated with gemfibrozil (n = 754) or placebo (n = 741). In this study, samples obtained at the 3-month visit were used; and data were analyzed prospectively using CVD events (coronary heart disease death, myocardial infarction, or stroke) during the 5.1 years of follow-up. Analyses in the gemfibrozil arm showed that subjects with recurrent CVD events had significantly higher prebeta-1 and had significantly lower alpha-1 and alpha-2 HDL levels than those without such events. Prebeta-1 level was a significant positive predictor; alpha-1 and alpha-2 levels were significant negative risk factors for future CVD events. alpha-2 level was superior to HDL cholesterol level in CVD-risk assessment after adjustment for established risk factors. Gemfibrozil treatment was associated with 3% to 6% decreases in the small, lipid-poor prebeta-1 HDL and in the large, lipid-rich alpha-1 and alpha-2 HDL and with increases in the small alpha-3 (3%) and prealpha-3 (16%) HDLs. Although the use of gemfibrozil has been associated with reduction in CVD events in VA-HIT, HDL subpopulation analysis indicates that gemfibrozil-mediated improvement in CVD risk might not be the result of its effects on HDL. It is quite possible that much of the cardiovascular benefits of gemfibrozil are due to a much wider spectrum of effects on metabolic processes that is not reflected by changes in blood lipids and HDL subpopulations.
在退伍军人事务部高密度脂蛋白干预试验(VA-HIT)中,心血管疾病(CVD)事件显著减少,而使用贝特类药物吉非贝齐使高密度脂蛋白(HDL)胆固醇升高6%并不能完全解释这一现象。我们研究了HDL亚群的测量是否能提供更多有关降低CVD风险的信息。在接受吉非贝齐治疗(n = 754)或安慰剂治疗(n = 741)的受试者中,通过二维凝胶电泳对HDL亚群进行了表征。在本研究中,使用了在3个月随访时获取的样本;并对随访5.1年期间的CVD事件(冠心病死亡、心肌梗死或中风)进行前瞻性数据分析。吉非贝齐组的分析表明,复发性CVD事件的受试者相比无此类事件的受试者,前β-1水平显著更高,而α-1和α-2 HDL水平显著更低。前β-1水平是未来CVD事件的显著正预测因子;α-1和α-2水平是未来CVD事件的显著负风险因素。在对既定风险因素进行调整后,α-2水平在CVD风险评估中优于HDL胆固醇水平。吉非贝齐治疗使小的、脂质含量低的前β-1 HDL以及大的、脂质含量高的α-1和α-2 HDL降低了3%至6%,并使小的α-3 HDL(3%)和前α-3 HDL(16%)升高。尽管在VA-HIT中使用吉非贝齐与CVD事件减少有关,但HDL亚群分析表明,吉非贝齐介导的CVD风险改善可能并非其对HDL作用的结果。很可能吉非贝齐对心血管的诸多益处归因于其对代谢过程更广泛的影响,而这并未通过血脂和HDL亚群的变化反映出来。