Rahimi Zohreh, Nourozi-Rad Reza, Vaisi-Raygani Asad, Saidi Mohammad-Reza, Rahimi Ziba, Ahmadi Reza, Yarani Reza, Hamzehee Koorosh, Parsian Abbas
Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Genet Test Mol Biomarkers. 2011 Nov;15(11):813-9. doi: 10.1089/gtmb.2011.0037. Epub 2011 Jun 20.
To shed light on the previously inconsistent results about the association of cholesteryl ester transfer protein TaqIB (CETP TaqIB) variants, high-density lipoprotein cholesterol (HDL-C) levels, and the risk of coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM).
To determine the frequency of CETP TaqIB variants and to examine the possible association between CETP TaqIB polymorphism with CAD and T2DM, we studied 207 unrelated patients with CAD, 101 patients with T2DM, and 92 controls. The CETP TaqIB variants were detected by polymerase chain reaction-restriction fragment length polymorphism.
Logistic regression analysis indicated that the B1 allele of CETP was significantly associated with increased risk of CAD (odds ratio, OR 1.65 [95% confidence interval, CI 1.2-2.3, p=0.005]) and T2DM (OR 1.7 [95% CI 1.13-2.54, p=0.005]). Adjusted logistic regression analysis for the effects of age, sex, hypertension, diabetes, and hyperlipidemia was performed; and a significant association was found between the B1 allele and risk of CAD (OR 1.9 [95% CI 1-3.6, p=0.049]) in patients with CAD. There were no associations between the CETP alleles and the levels of triglycerides, total cholesterol, low-density lipoprotein cholesterol, and HDL-C in studied groups.
The results of the present study revealed that the CETP B1 allele is associated with increased risk of CAD and T2DM independent of plasma HDL-C level in our population.
阐明此前关于胆固醇酯转运蛋白TaqIB(CETP TaqIB)变体、高密度脂蛋白胆固醇(HDL-C)水平与冠状动脉疾病(CAD)及2型糖尿病(T2DM)风险之间关联的不一致结果。
为确定CETP TaqIB变体的频率,并检验CETP TaqIB多态性与CAD和T2DM之间的可能关联,我们研究了207例无亲缘关系的CAD患者、101例T2DM患者及92例对照。通过聚合酶链反应-限制性片段长度多态性检测CETP TaqIB变体。
逻辑回归分析表明,CETP的B1等位基因与CAD风险增加显著相关(优势比,OR 1.65 [95%置信区间,CI 1.2 - 2.3,p = 0.005])以及T2DM风险增加显著相关(OR 1.7 [95% CI 1.13 - 2.54,p = 0.005])。对年龄、性别、高血压、糖尿病和高脂血症的影响进行了校正逻辑回归分析;在CAD患者中发现B1等位基因与CAD风险之间存在显著关联(OR 1.9 [95% CI 1 - 3.6,p = 0.049])。在研究组中,CETP等位基因与甘油三酯、总胆固醇、低密度脂蛋白胆固醇及HDL-C水平之间无关联。
本研究结果显示,在我们的人群中,CETP B1等位基因与CAD和T2DM风险增加相关,且独立于血浆HDL-C水平。