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Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitus

机译:内皮型一氧化氮合酶的T等位基因与胆固醇酯转移蛋白TaqIB的B1等位基因之间的强相互作用极大地增加了冠心病和2型糖尿病的风险

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Background The present study was conducted to investigate the possible outcome of interaction between endothelial nitric oxide ( NOS3 ) G894T and cholesteryl ester transfer TaqIB variants on the risk of coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM). The sample included a total of 207 CAD patients (102 CAD patients with T2DM and 105 CAD patients without T2DM). There were also 101 patients with T2DM and 92 age- and sex-matched healthy individuals as controls. All study participants were from Western Iran. The sample was genotyped by polymerase chain reaction-restriction fragment length polymorphism. Results The presence of NOS3 T allele was not associated with the risk of CAD or T2DM, and the CETP B1 allele was only significantly associated with the increased risk of CAD in total CAD patients (odds ratio (OR)?=?5.1, p =?0.019). However, the concomitant presence of both CETP B1 and NOS3 T alleles significantly increased the risk of CAD in total CAD patients (OR?=?18.1, p p =?0.03), and in CAD patients with T2DM (OR?=?13.5, p =?0.002). Also, the presence of both alleles increased the risk of T2DM (OR?=?12, p =?0.004). Conclusions Our findings, for the first time, indicate that NOS3 T allele strongly interacts with CETP B1 allele to augment the risk of CAD and T2DM in the population of Western Iran.
机译:背景本研究旨在研究内皮型一氧化氮(NOS3)G894T和胆固醇酯转移TaqIB变体之间相互作用对冠心病(CAD)和2型糖尿病(T2DM)风险的可能结果。该样本总共包括207位CAD患者(102位患有T2DM的CAD患者和105位没有T2DM的CAD患者)。还有101例T2DM患者和92名年龄和性别匹配的健康个体作为对照。所有研究参与者均来自伊朗西部。通过聚合酶链反应-限制性片段长度多态性对样品进行基因分型。结果NOS3 T等位基因的存在与CAD或T2DM的风险无关,而CETP B1等位基因仅与总CAD患者的CAD风险增加显着相关(优势比(OR)?=?5.1,p = 0.019)。然而,CETP B1和NOS3 T等位基因的同时存在显着增加了总CAD患者(OR?=?18.1,pp =?0.03)和患有T2DM的CAD患者(OR?=?13.5,p =?0.002)。而且,两个等位基因的存在增加了T2DM的风险(ORα=≤12,p =≤0.004)。结论我们的发现首次表明,NOS3 T等位基因与CETP B1等位基因强烈相互作用,从而增加了伊朗西部人群CAD和T2DM的风险。

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