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Association between insulin receptor gene polymorphism and the metabolic syndrome in Han and Yi Chinese.

机译:汉族和彝族人群胰岛素受体基因多态性与代谢综合征的相关性。

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摘要

Insulin resistance has been a possible underlying pathophysiologic defect inducing the metabolic syndrome (MS). However association studies regarding Insulin receptor gene in different ethnic groups are scarce in literature. Here we conduct an association study between MS and genetic polymorphism of the INSR gene in Yi and Han Chinese. In a cross-sectional study, 3,436 Yi and Han people were investigated. Ethnicity-specific case-control studies were designed, with MS patients diagnosed as cases and non-MS people as controls matched on gender and age. Polymerase chain reaction-restriction fragment length polymorphism was used to detect the genotypes of the exon 8 of the INSR gene. Data were analyzed using one-way analysis of variance, chi-square test, and logistic regression where appropriate. Systolic blood pressure (SBP) was significantly higher in MS patients with the N1N2/N2N2 genotypes than that in those with the N1N1 genotype of both ethnic population (p<0.05). Frequency of the N2 allele was significantly higher in MS patients than that in controls of ethnic Han (p=0.020). Multivariable logistic regression analysis showed that the NsiI polymorphism of the exon 8 of the INSR was an independent predictor for MS in Han people adjusted for total cholesterol, sex, physical activity, educational level, family income, alcohol intake and smoking (OR=2.55, 95% CI: 1.31-4.94, p=0.006). The results indicated that NsiI polymorphism of the INSR gene is associated with SBP in these two different ethnic groups, and significantly associate with MS in Han Chinese. These findings contribute to our better understanding on the genetic basis of MS.
机译:胰岛素抵抗可能是引起代谢综合征(MS)的潜在病理生理缺陷。但是,关于不同种族的胰岛素受体基因的关联研究在文献中很少。在这里,我们进行了MS和彝族和汉族INSR基因遗传多态性之间的关联研究。在一项横断面研究中,调查了3436名彝族和汉族。设计了针对特定种族的病例对照研究,将MS患者诊断为病例,将非MS患者诊断为性别和年龄相匹配的对照。用聚合酶链反应-限制性片段长度多态性检测INSR基因第8外显子的基因型。在适当的情况下,使用单向方差分析,卡方检验和逻辑回归分析数据。 N1N2 / N2N2基因型的MS患者的收缩压(SBP)显着高于两个民族人群的N1N1基因型的患者(p <0.05)。 MS患者中N2等位基因的频率显着高于汉族人群(p = 0.020)。多变量logistic回归分析显示,INSR外显子8的NsiI多态性是汉族人群MS的独立预测因子,对汉族人群的总胆固醇,性别,身体活动,教育程度,家庭收入,饮酒和吸烟进行了调整(OR = 2.55, 95%CI:1.31-4.94,p = 0.006)。结果表明,在这两个不同的族裔中,INSR基因的NsiI多态性与SBP相关,并与汉族的MS显着相关。这些发现有助于我们更好地了解MS的遗传基础。

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