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IRS1、TCF7L2、ADRB1、PPARG和HHEX基因多态性与墨西哥人群的动脉粥样硬化风险相关。

IRS1, TCF7L2, ADRB1, PPARG, and HHEX polymorphisms associated with atherogenic risk in Mexican population.

作者信息

Estrada-Velasco B I, Cruz M, Madrid-Marina V, Martínez-Nava G A, Gomez-Zamudio J, Burguete-García A I

机构信息

Centro de Enfermedades Infecciosas, Instituto Nacional de Salud Pública, Avenida Universidad 655, Santa María Ahuacatitlán, Cuernavaca, 62100 Cuernavaca, MOR, Mexico.

Unidad de Investigación Médica en Bioquímica, Hospital de Especialidades, IMSS, Avenida Cuauhtémoc 330, Doctores, Cuauhtémoc, CMN Siglo XXI, 06720 México, DF, Mexico.

出版信息

Biomed Res Int. 2013;2013:394523. doi: 10.1155/2013/394523. Epub 2013 Nov 25.

Abstract

Objective. We aimed to explore the association between polymorphisms of IRS1 (rs1801278), TCF7L2 (rs7903146 and rs12255372), ADRB1 (rs1801253), PPARG (rs1801282), and HHEX (rs5015480) genes with atherogenic risk (AI = Total cholesterol/HDL) in MetS, T2D, and healthy populations from the Mexican Social Security Institute. Methodology and Results. Four hundred thirty-five MetS, 517 T2D, and 547 healthy individuals were selected. The association between the SNPs and the atherogenic index was evaluated by multiple linear regression and multinomial logistic regression models. The ADRB1 gene showed a statistically significant association with high-risk atherogenic index, OR = 2.94 (IC 95% 1.64-5.24; P < 0.0001) for the Arg/Gly variant, under the dominant model an OR = 2.96 (IC 95% 1.67-5.25; P < 0.0001), and under the Log additive model an OR = 2.52 (IC 95% 1.54-4.15; P < 0.0001). Conclusions. The Arg389Gly polymorphism of the ADRB1 gene may be a worthy biological marker to predict the risk of developing cardiovascular diseases given a high-risk atherogenic index.

摘要

目的。我们旨在探讨墨西哥社会保障机构的代谢综合征(MetS)、2型糖尿病(T2D)和健康人群中胰岛素受体底物1(IRS1,rs1801278)、转录因子7样蛋白2(TCF7L2,rs7903146和rs12255372)、β1肾上腺素能受体(ADRB1,rs1801253)、过氧化物酶体增殖物激活受体γ(PPARG,rs1801282)和肝细胞核因子1α(HHEX,rs5015480)基因多态性与致动脉粥样硬化风险(AI = 总胆固醇/高密度脂蛋白)之间的关联。方法与结果。选取了435例代谢综合征患者、517例2型糖尿病患者和547例健康个体。通过多元线性回归和多项逻辑回归模型评估单核苷酸多态性(SNP)与致动脉粥样硬化指数之间的关联。ADRB1基因与高风险致动脉粥样硬化指数存在统计学显著关联,在显性模型下,Arg/Gly变异的比值比(OR)= 2.94(95%置信区间[IC] 1.64 - 5.24;P < 0.0001),在对数加性模型下,OR = 2.96(95% IC 1.67 - 5.25;P < 0.0001),在对数加性模型下,OR = 2.52(95% IC 1.54 - 4.15;P < 0.0001)。结论。鉴于高风险致动脉粥样硬化指数,ADRB1基因的Arg389Gly多态性可能是预测心血管疾病发生风险的一个有价值的生物学标志物。

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