Mohammadzadeh Ghorban, Ghaffari Mohammad-Ali, Heibar Habib, Bazyar Mohammad
Hyperlipidemia Research Center, Dept. of Clinical Biochemistry, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Cellular and Molecular Research Center, Dept. of Clinical Biochemistry, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Iran Biomed J. 2016 Jul;20(3):152-60. doi: 10.7508/ibj.2016.03.004. Epub 2016 Jan 19.
Adiponectin, an adipocyte-secreted hormone, is known to have anti-atherogenic, anti-inflammatory, and anti-diabetic properties. In the present study, the association between two common single nucleotide polymorphisms (SNPs) (+45T/G and +276G/T) of ADIOPQ gene and coronary artery disease (CAD) was assessed in the subjects with type 2 diabetes (T2DM).
Genotypes of two SNPs were determined by polymerase chain reaction-restriction fragment length polymorphism in 200 subjects with T2DM (100 subjects with CAD and 100 without CAD).
The frequency of TT genotype of +276G/T was significantly elevated in CAD compared to controls (χ2=7.967, P=0.019). A similar difference was found in the allele frequency of +276G/T between two groups (χ2=3.895, P=0.048). The increased risk of CAD was associated with +276 TT genotype when compared to reference GG genotype (OR=5.158; 95% CI=1.016-26.182, P=0.048). However, no similar difference was found in genotype and allele frequencies of SNP +45T/G between two groups. There was a CAD protective haplotype combination of +276 wild-type and +45 mutant-type allele (276G-45G) (OR=0.37, 95% CI=0.16-0.86, P=0.022) in the subject population.
Our findings indicated that T allele of SNP +276G/T is more associated with the increased risk of CAD in subjects with T2DM. Also, a haplotype combination of +45G/+276G of these two SNPs has a protective effect on the risk of CAD.
脂联素是一种由脂肪细胞分泌的激素,已知具有抗动脉粥样硬化、抗炎和抗糖尿病特性。在本研究中,对2型糖尿病(T2DM)患者中脂联素基因(ADIPQ)的两个常见单核苷酸多态性(SNP)(+45T/G和+276G/T)与冠状动脉疾病(CAD)之间的关联进行了评估。
采用聚合酶链反应-限制性片段长度多态性方法,对200例T2DM患者(100例CAD患者和100例无CAD患者)的两个SNP进行基因分型。
与对照组相比,CAD患者中+276G/T的TT基因型频率显著升高(χ2=7.967,P=0.019)。两组间+276G/T的等位基因频率也存在类似差异(χ2=3.895,P=0.048)。与参考GG基因型相比,+276 TT基因型使CAD风险增加(OR=5.158;95%CI=1.016-26.182,P=0.048)。然而,两组间SNP +45T/G的基因型和等位基因频率未发现类似差异。在研究人群中,存在一种CAD保护性单倍型组合,即+276野生型和+45突变型等位基因(276G-45G)(OR=0.37,95%CI=0.16-0.86,P=0.022)。
我们的研究结果表明,SNP +276G/T的T等位基因与T2DM患者CAD风险增加更相关。此外,这两个SNP的+45G/+276G单倍型组合对CAD风险具有保护作用。