Corella D, Sáiz C, Guillén M, Portolés O, Mulet F, González J I, Ordovás J M
Genetic and Molecular Epidemiology Unit, Public Health Department, School of Medicine, Universitat de València, Valencia, Spain.
Atherosclerosis. 2000 Oct;152(2):367-76. doi: 10.1016/s0021-9150(99)00477-3.
Genetic variants at the cholesteryl ester transfer protein (CETP) locus have been associated with CETP activity and mass, as well as plasma high density lipoprotein cholesterol (HDL-C) and apolipoprotein A-I levels. We have examined allele frequencies and lipid associations for the common CETP TaqIB polymorphism in a sample of 514 healthy subjects (231 men, mean age 37.4 years, and 283 women, mean age 35.7 years) residing in Valencia (Spain). The frequency of the less common TaqIB2 allele (0.351; 95% CI: 0.322-0. 380) was significantly lower than those reported for Northern European populations. Consistent with previous studies, we found a significant association of the TaqIB polymorphism with HDL-C levels. Homozygotes for the B1 allele had lower HDL-C levels than subjects carrying the B2 allele (P trend<0.001 and 0.002, for men and women, respectively). No statistically significant genotype effects were observed for any of the other lipid measures. Multivariate models including TaqIB genotype, body mass index, smoking, alcohol, physical activity, marital status and education were fitted to predict HDL-C levels. The TaqIB polymorphism was consistently an independent predictor of HDL-C levels (P<0.001), and explained 5.8% of its variance. To evaluate gene-environmental interactions, first order interaction terms were tested into the multivariate model. No statistically significant interactions between the TaqIB genotypes and smoking, alcohol, physical activity or education were detected. In conclusion, we observed a significant association of the TaqIB polymorphism with HDL-C levels, which remained consistent across different levels of behavioral factors. Moreover, we found that the TaqIB2 allele frequency was lower in our sample than in other European populations, which could be a contributing factor to the unexpectedly high prevalence of coronary heart disease observed in the region of Valencia.
胆固醇酯转运蛋白(CETP)基因座的遗传变异与CETP活性、质量以及血浆高密度脂蛋白胆固醇(HDL-C)和载脂蛋白A-I水平相关。我们在居住于西班牙巴伦西亚的514名健康受试者(231名男性,平均年龄37.4岁;283名女性,平均年龄35.7岁)样本中,研究了常见的CETP TaqIB多态性的等位基因频率和脂质关联。较不常见的TaqIB2等位基因频率(0.351;95%置信区间:0.322 - 0.380)显著低于北欧人群报告的频率。与先前研究一致,我们发现TaqIB多态性与HDL-C水平存在显著关联。B1等位基因纯合子的HDL-C水平低于携带B2等位基因的受试者(男性和女性的P趋势分别<0.001和0.002)。对于任何其他脂质指标,均未观察到具有统计学意义的基因型效应。构建了包括TaqIB基因型、体重指数、吸烟、饮酒、体育活动、婚姻状况和教育程度的多变量模型来预测HDL-C水平。TaqIB多态性始终是HDL-C水平的独立预测因子(P<0.001),并解释了其5.8%的变异。为评估基因 - 环境相互作用,将一阶相互作用项纳入多变量模型进行检验。未检测到TaqIB基因型与吸烟、饮酒、体育活动或教育程度之间具有统计学意义的相互作用。总之,我们观察到TaqIB多态性与HDL-C水平存在显著关联,在不同行为因素水平下均保持一致。此外,我们发现我们样本中的TaqIB2等位基因频率低于其他欧洲人群,这可能是巴伦西亚地区冠心病患病率意外高的一个促成因素。