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首页> 外文期刊>Clinical Endocrinology >Association of AGER gene G82S polymorphism with the severity of coronary artery disease in Chinese Han population.
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Association of AGER gene G82S polymorphism with the severity of coronary artery disease in Chinese Han population.

机译:AGER基因G82S多态性与中国汉族人群冠心病严重程度的关系。

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BACKGROUND AND OBJECTIVE: Advanced glycosylation end-product receptor (AGER) plays an important role in the development and progression of atherosclerosis. The G82S polymorphism (rs2070600) is located in the ligand-binding V-domain of AGER suggesting a possible influence of this variant on AGER function. The aim of this study is to evaluate the association of the G82S polymorphism with the severity of coronary artery disease (CAD) in patients with or without type 2 diabetes mellitus (T2DM). DESIGN AND METHODS: The AGER gene G82S polymorphism was analysed in 270 nondiabetic and 270 type 2 diabetic Chinese Han patients with angiographically proven CAD (luminal stenosis >/= 50%). The number of diseased vessels and Gensini score were used to determine the severity of CAD. Genotyping for the G82S polymorphism was performed by PCR-RFLP using restriction enzymes AluI. RESULTS: The frequency of 82S allele was significantly lower in the diabetic CAD patients with multi-vessel disease than in those with single-vessel disease (P = 0.015). When controlled for confounding variables, the 82S allele was associated with decreased risk of multi-vessel disease [P = 0.038, adjusted OR = 0.565 (0.329-0.972)]. The protective effect of the 82S allele against the severity of CAD was not observed in patients with nondiabetic CAD. CONCLUSIONS: AGER 82S allele showed a protective effect on CAD severity in the presence of T2DM in Chinese Han population.
机译:背景与目的:晚期糖基化终产物受体(AGER)在动脉粥样硬化的发生发展中起重要作用。 G82S多态性(rs2070600)位于AGER的配体结合V结构域中,表明此变体可能对AGER功能产生影响。这项研究的目的是评估G82S多态性与有无2型糖尿病(T2DM)的冠状动脉疾病(CAD)严重程度的关系。设计与方法:分析了270例经血管造影证实为CAD(管腔狭窄> / = 50%)的非糖尿病和270名2型糖尿病中国汉族患者的AGER基因G82S多态性。使用患病血管的数量和Gensini评分确定CAD的严重程度。使用限制酶AluI,通过PCR-RFLP对G82S多态性进行基因分型。结果:糖尿病CAD患者多支血管疾病的82S等位基因频率明显低于单支血管疾病的患者(P = 0.015)。当控制混杂变量时,82S等位基因与多支血管疾病的风险降低相关[P = 0.038,调整后的OR = 0.565(0.329-0.972)]。在非糖尿病CAD患者中未观察到82S等位基因对CAD严重程度的保护作用。结论:在中国汉族人群中,在存在T2DM的情况下,AGER 82S等位基因显示出对CAD严重程度的保护作用。

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