首页> 美国卫生研究院文献>Mediators of Inflammation >Interleukin 35 Polymorphisms Are Associated with Decreased Risk of Premature Coronary Artery Disease Metabolic Parameters and IL-35 Levels: The Genetics of Atherosclerotic Disease (GEA) Study
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Interleukin 35 Polymorphisms Are Associated with Decreased Risk of Premature Coronary Artery Disease Metabolic Parameters and IL-35 Levels: The Genetics of Atherosclerotic Disease (GEA) Study

机译:白细胞介素35多态性与冠状动脉疾病代谢参数和IL-35水平降低的风险相关:动脉粥样硬化疾病(GEA)的遗传学研究

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摘要

Interleukin 35 (IL-35) is a heterodimeric cytokine involved in the development of atherosclerosis. The aim of the present study was to establish if the polymorphisms of IL-12A and EBI3 genes that encode the IL-35 subunits are associated with the development of premature coronary artery disease (CAD) in Mexican individuals. The IL-12A and EBI3 polymorphisms were determined in 1162 patients with premature CAD and 873 controls. Under different models, the EBI3 rs428253 (OR = 0.831, Padd = 0.036; OR = 0.614, Prec = 0.033; OR = 0.591, Pcod2 = 0.027) and IL-12A rs2243115 (OR = 0.674, Padd = 0.010; OR = 0.676, Pdom = 0.014; OR = 0.698, Phet = 0.027; OR = 0.694, Pcod1 = 0.024) polymorphisms were associated with decreased risk of developing premature CAD. Some polymorphisms were associated with clinical and metabolic parameters. Significant different levels of IL-35 were observed in EBI3 rs4740 and rs4905 genotypes only in the group of healthy controls. In summary, our study suggests that the EBI3 and IL-12A polymorphisms play an important role in decreasing the risk of developing premature CAD; it also demonstrates the relationship of the EBI3 rs4740 and rs4905 genotypes with IL-35 levels in healthy individuals.
机译:白介素35(IL-35)是一种异二聚体细胞因子,参与动脉粥样硬化的发展。本研究的目的是确定墨西哥个体中编码IL-35亚基的IL-12A和EBI3基因多态性是否与早发冠状动脉疾病(CAD)的发生有关。 IL-12A和EBI3多态性在1162例CAD早期患者和873例对照中确定。在不同模型下,EBI3 rs428253(OR = 0.831,Padd = 0.036; OR = 0.614,Prec = 0.033; OR = 0.591,Pcod2 = 0.027)和IL-12A rs2243115(OR = 0.674,Padd = 0.010; OR = 0.676, Pdom = 0.014; OR = 0.698,Phet = 0.027; OR = 0.694,Pcod1 = 0.024)多态性与降低过早CAD的风险相关。一些多态性与临床和代谢参数有关。仅在健康对照组中,在EBI3 rs4740和rs4905基因型中观察到了显着不同的IL-35水平。总而言之,我们的研究表明EBI3和IL-12A多态性在降低过早发生CAD的风险中起着重要作用。它还证明了健康个体中 EBI3 rs4740和rs4905基因型与IL-35水平的关系。

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