Alteration in microRNA-146a (miRNA-146a) expression is an important event in the pathogenesis of many human diseases. MiRNA-146a rs2910164 is a functional polymorphism that showed association with several diseases. Metabolic syndrome is an aggregation of multiple risk factors including impaired glucose tolerance, increased highdensity lipoprotein, abdominal obesity, and high blood pressure. The aim of this study was to assess the relation of miRNA-146a rs2910164 with metabolic syndrome and its component traits in Egyptian women from the Suez Canal area. The study included 100 healthy female subjects and 100 metabolic syndrome patients. The component traits of metabolic syndrome were determined and the genotypes of the polymorphisms were assessed using the polymerase chain reaction-restriction fragment length polymorphism technique using the restriction enzyme Hpy188I. The rare C allele had a significantly higher frequency in metabolic syndrome patients (P = 0.013). The heterozygote GC and the rare CC genotypes showed a significant increase in body mass index, waist circumference, triglycerides, total cholesterol, low-density lipoprotein, systolic and diastolic blood pressure. The GC genotype was associated with higher fasting blood glucose, fasting serum insulin and insulin resistance. The carriers of CC genotype had significantly lower HDL compared with the GG genotype carriers. In conclusion, The C allele of miRNA-146a rs2910164 showed positive association with increased susceptibility to metabolic syndrome and its phenotypes in the study population.

译文

:microRNA-146a(miRNA-146a)表达的改变是许多人类疾病发病机理中的重要事件。 MiRNA-146a rs2910164是一种功能性多态性,显示与多种疾病相关。代谢综合征是多种危险因素的综合,包括葡萄糖耐量降低,高密度脂蛋白增加,腹部肥胖和高血压。这项研究的目的是评估苏伊士运河地区的埃及妇女中miRNA-146a rs2910164与代谢综合征及其组成特征的关系。该研究包括100名健康女性受试者和100名代谢综合征患者。使用限制酶Hpy188I,通过聚合酶链反应-限制性片段长度多态性技术,确定代谢综合征的组成特征,并评估多态性的基因型。罕见的C等位基因在代谢综合征患者中的发生频率显着更高(P = 0.013)。杂合子GC和罕见的CC基因型显示出体重指数,腰围,甘油三酸酯,总胆固醇,低密度脂蛋白,收缩压和舒张压显着增加。 GC基因型与较高的空腹血糖,空腹血清胰岛素和胰岛素抵抗有关。与GG基因型携带者相比,CC基因型携带者具有显着更低的HDL。总之,在研究人群中,miRNA-146a rs2910164的C等位基因与代谢综合征及其表型的敏感性增加呈正相关。

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