Ghazouani Lakhdar, Elmufti Afoua, Baaziz Intissar, Chaabane Ibtissem, Ben Mansour Hedi
Research Unit of Macromolecular Biochemistry and Genetics, Faculty of Sciences of Gafsa, Gafsa, Tunisia.
Research Unit of Analysis and Process Applied to the Environmental-APAE (UR17ES32), Higher Institute of Applied Sciences and Technology Mahdia, University of Monastir, Monastir, Tunisia.
J Clin Lab Anal. 2018 Sep;32(7):e22446. doi: 10.1002/jcla.22446. Epub 2018 Apr 6.
Adiponectin, an adipocyte-derived protein, is known to play a key role in the processes leading to atherosclerosis and coronary artery disease (CAD) through its anti-atherogenic, anti-inflammatory, antioxidative, and anti-apoptotic properties. In the current study, we have studied the association of two single nucleotide polymorphisms (SNPs) +45 T>G (rs2241766) and +276 G>T (rs1501299) of the adiponectin gene with coronary artery disease (CAD) on an Arab/North-African population from Tunisia.
Subjects comprised 277 patients with angiographically demonstrated CAD and 269 age- and gender-matched control subjects. The adiponectin genotypes were performed by polymerase chain reaction-restriction fragment length polymorphism analysis (PCR-RFLP). The contribution of adiponectin variants to CAD was analyzed by haplotype and regression analysis.
Adiponectin +45T>G and +276G>T genotypic and allelic distributions did not show a significant difference between cases and controls. Similarly, no association with CAD was observed for the haplotype analysis. Assuming dominant model of transmission for both polymorphisms and after adjustment of a number of traditional risk factors for CAD, logistic regression analysis showed an association of SNP +45 T>G with increased risk of developing CAD [adjusted OR (95% CI) = 2.59 (1.17-5.70); P = .01]. However, SNP + 276 G>T is associated with decreased risk of developing CAD [adjusted OR (95% CI) = 0.47 (0.22-0.97); P = .04].
There is no allelic or genotypic association of +45 T>G and +276 G>T of the adiponectin gene with CAD in the Tunisian population.
脂联素是一种脂肪细胞衍生蛋白,已知其通过抗动脉粥样硬化、抗炎、抗氧化和抗凋亡特性,在导致动脉粥样硬化和冠状动脉疾病(CAD)的过程中发挥关键作用。在本研究中,我们在来自突尼斯的阿拉伯/北非人群中,研究了脂联素基因的两个单核苷酸多态性(SNP)+45 T>G(rs2241766)和+276 G>T(rs1501299)与冠状动脉疾病(CAD)的关联。
研究对象包括277例经血管造影证实患有CAD的患者和269例年龄及性别匹配的对照者。通过聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)进行脂联素基因分型。通过单倍型和回归分析,分析脂联素变异对CAD的影响。
脂联素+45T>G和+276G>T的基因型和等位基因分布在病例组和对照组之间未显示出显著差异。同样,单倍型分析未观察到与CAD的关联。假设两种多态性均为显性遗传模式,并在调整了一些CAD的传统危险因素后,逻辑回归分析显示SNP +45 T>G与CAD发生风险增加相关[调整后的比值比(95%置信区间)= 2.59(1.17 - 5.70);P = 0.01]。然而,SNP +276 G>T与CAD发生风险降低相关[调整后的比值比(95%置信区间)= 0.47(0.22 - 0.97);P = 0.04]。
在突尼斯人群中,脂联素基因的+45 T>G和+276 G>T与CAD不存在等位基因或基因型关联。