在高密度脂蛋白缺乏的男性中,胆固醇酯转移蛋白Taq I B2B2基因型与较高的高密度脂蛋白胆固醇水平和较低的冠心病风险终点相关:退伍军人事务部高密度脂蛋白胆固醇干预试验

M. Brousseau, J. O’Connor, J. Ordovás, D. Collins, J. Otvos, T. Massov, J. Mcnamara, H. Rubins, S. Robins, E. Schaefer
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引用次数: 166

摘要

目的:我们之前在Framingham后代研究(FOS)中报道了胆固醇酯转移蛋白(CETP) Taq IB位点的遗传变异与血浆脂质水平和冠心病(CHD)风险相关。在FOS中,B2等位基因与具有B2B2基因型的男性高密度脂蛋白(HDL)胆固醇(HDL- c)水平升高、CETP活性降低以及冠心病风险降低相关。本研究旨在进一步确定这种多态性与人群水平上冠心病风险之间的关系。方法和结果:我们在参加退伍军人事务HDL- c干预试验(VA-HIT)的852名男性中检测了CETP Taq IB基因型与血浆脂蛋白水平、对吉非罗齐治疗的反应和冠心病终点之间的关系。VA-HIT是一项研究,旨在探讨在以低HDL- c(≤40 mg/dL)为主要脂质异常的冠心病男性中提高HDL水平的潜在益处。VA-HIT中有13.9%的男性具有B2B2基因型,而FOS中有19.1%的男性具有B1B1基因型(- 27%,P <0.03),而VA-HIT中有更多的男性具有B1B1基因型(15%,P <0.05)。与我们在FOS中的发现相似,VA-HIT中B2B2男性的HDL-C平均水平最高(32.6±4.8 mg/dL),其次是B1B2男性(32.0±5.3 mg/dL),最后是B1B1男性(30.9±4.9 mg/dL)。有趣的是,基线时血脂状况最不利的B1B1男性对吉非罗齐有最大的甘油三酯降低反应(- 34%,P =0.006)。CETP Taq IB基因型也与VA-HIT中冠心病终点的风险相关,B2B2男性的调整风险比为0.52 (P =0.08)。结论:我们的数据表明,在冠心病和高密度脂蛋白缺乏的男性中,CETP Taq I B2B2基因型(1)显著降低,(2)与血浆高密度脂蛋白c水平升高和冠心病风险降低相关。与我们之前的报告一起,这些结果支持了CETP活性降低导致HDL-C水平升高与冠心病风险降低相关的概念。
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Cholesteryl Ester Transfer Protein Taq I B2B2 Genotype Is Associated With Higher HDL Cholesterol Levels and Lower Risk of Coronary Heart Disease End Points in Men With HDL Deficiency: Veterans Affairs HDL Cholesterol Intervention Trial
Objective—We have previously reported that genetic variation at the cholesteryl ester transfer protein (CETP) Taq IB locus is correlated with plasma lipid levels and coronary heart disease (CHD) risk in the Framingham Offspring Study (FOS). In FOS, the B2 allele was associated with increased levels of high density lipoprotein (HDL) cholesterol (HDL-C), decreased CETP activity, and reduced CHD risk for men having the B2B2 genotype. The present study was undertaken to further define the relationship between this polymorphism and CHD risk at the population level. Methods and Results—We tested for associations between the CETP Taq IB genotype and plasma lipoprotein levels, response to gemfibrozil therapy, and CHD end points in 852 men participating in the Veterans Affairs HDL-C Intervention Trial (VA-HIT), a study designed to explore the potential benefits of raising HDL levels in men having established CHD with low HDL-C (≤40 mg/dL) as their primary lipid abnormality. In VA-HIT, 13.9% of the men had the B2B2 genotype relative to 19.1% of the men in FOS (−27%, P <0.03), whereas more men in VA-HIT had the B1B1 genotype (15%, P <0.05). Similar to our finding in FOS, B2B2 men in VA-HIT had the highest mean level of HDL-C (32.6±4.8 mg/dL), followed by B1B2 men (32.0±5.3 mg/dL), and, last, by B1B1 men (30.9±4.9 mg/dL). Interestingly, B1B1 men, who had the least favorable plasma lipid profile at baseline, had the greatest triglyceride-lowering response to gemfibrozil (−34%, P =0.006). CETP Taq IB genotype was also associated with the risk of CHD end points in VA-HIT, with an adjusted risk ratio of 0.52 for B2B2 men (P =0.08). Conclusions—Our data demonstrate that in men with CHD and HDL deficiency, the CETP Taq I B2B2 genotype is (1) significantly reduced and (2) associated with higher levels of plasma HDL-C and lower CHD risk. Together with our earlier report, these results support the concept that increased HDL-C levels, resulting from reduced CETP activity, are associated with decreased CHD risk.
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