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胆固醇酯转运蛋白TaqI B2B2基因型与高密度脂蛋白缺乏男性的较高高密度脂蛋白胆固醇水平及较低冠心病终点风险相关:退伍军人事务部高密度脂蛋白胆固醇干预试验

Cholesteryl ester transfer protein TaqI 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.

作者信息

Brousseau Margaret E, O'Connor John J, Ordovas Jose M, Collins Dorothea, Otvos James D, Massov Tatyana, McNamara Judith R, Rubins Hanna B, Robins Sander J, Schaefer Ernst J

机构信息

Lipid Metabolism Laboratory, JM-USDA-Human Nutrition Research Center on Aging at Tufts University and Department of Medicine, New England Medical Center, Boston, Mass 02111, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2002 Jul 1;22(7):1148-54. doi: 10.1161/01.atv.0000024566.57589.2e.

Abstract

OBJECTIVE

We have previously reported that genetic variation at the cholesteryl ester transfer protein (CETP) TaqIB 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 TaqIB 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 (< or =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 TaqIB 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 TaqI 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.

摘要

目的

我们之前在弗雷明汉后代研究(FOS)中报告,胆固醇酯转运蛋白(CETP)TaqIB位点的基因变异与血浆脂质水平及冠心病(CHD)风险相关。在FOS中,B2等位基因与高密度脂蛋白(HDL)胆固醇(HDL-C)水平升高、CETP活性降低以及B2B2基因型男性的CHD风险降低相关。本研究旨在进一步明确该多态性与人群水平CHD风险之间的关系。

方法与结果

我们在852名参与退伍军人事务部HDL-C干预试验(VA-HIT)的男性中,检测了CETP TaqIB基因型与血浆脂蛋白水平、对吉非贝齐治疗的反应以及CHD终点之间的关联。VA-HIT是一项旨在探索提高HDL水平对以低HDL-C(≤40mg/dL)为主要脂质异常的已确诊CHD男性潜在益处的研究。在VA-HIT中,13.9%的男性为B2B2基因型,而FOS中这一比例为19.1%(-27%,P<0.03),同时VA-HIT中更多男性为B1B1基因型(15%,P<0.05)。与我们在FOS中的发现相似,VA-HIT中B2B2基因型男性的HDL-C平均水平最高(32.6±4.8mg/dL),其次是B1B2基因型男性(32.0±5.3mg/dL),最后是B1B1基因型男性(30.9±4.9mg/dL)。有趣的是,基线时血浆脂质谱最不理想的B1B1基因型男性,对吉非贝齐的甘油三酯降低反应最大(-34%,P=0.006)。CETP TaqIB基因型在VA-HIT中也与CHD终点风险相关,B2B2基因型男性的调整风险比为0.52(P=0.08)。

结论

我们的数据表明,在患有CHD和HDL缺乏的男性中,CETP TaqI B2B2基因型(1)显著降低,(2)与较高的血浆HDL-C水平及较低的CHD风险相关。连同我们之前的报告,这些结果支持了因CETP活性降低导致HDL-C水平升高与CHD风险降低相关的概念。

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