首页> 美国卫生研究院文献>Disease Markers >The Gly482Ser Missense Mutation of the Peroxisome Proliferator-Activated Receptor γ Coactivator-1α (PGC-1α) Gene Associates with Reduced Insulin Sensitivity in Normal and Glucose-Intolerant Obese Subjects
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The Gly482Ser Missense Mutation of the Peroxisome Proliferator-Activated Receptor γ Coactivator-1α (PGC-1α) Gene Associates with Reduced Insulin Sensitivity in Normal and Glucose-Intolerant Obese Subjects

机译:正常人和葡萄糖耐量性肥胖者中过氧化物酶体增殖物激活的受体γ共激活因子-1α(PGC-1α)基因的Gly482Ser错义突变与胰岛素敏感性降低相关。

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摘要

Among the putative candidate genes for insulin resistance, the peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) is a transcriptional coactivator of PPARγ and α, regulating a wide range of processes involved in energy production and utilization, such as thermogenesis, liver gluconeogenesis, glucose uptake in muscle. In population studies a Gly482Ser substitution in PGC-1α has been reported to be associated with increased risk of type diabetes 2 and insulin resistance. In the present study we have analysed the association between the Gly482Ser missense mutation of the PGC-1α gene and insulin sensitivity and glucose tolerance in a population of obese non-diabetic subjects. The Gly482Ser SNPs was detected by PCR-RFLP in a cohort of 358 Caucasian obese subjects (223 with normal glucose tolerance (NGT) and 125 with impaired glucose tolerance (IGT). We observed a significant association (p < 0.007) between carriers of the Gly482Ser variant of the PGC-1α gene and insulin resistance measured by HOMAIR. Multivariate analysis confirmed that the Gly482Ser SNP was a significant (p < 0.02) determinant of decreased insulin sensitivity, independently from other well-known modulators of insulin action. In conclusion, we have found significant association between the Gly482Ser variant of the PGC-1α gene and reduced insulin sensitivity in obese subjects. This association resulted independent from all other known modulators of insulin resistance, and suggests a primary role for the PGC-1α gene on the genetic susceptibility to insulin resistance in obesity.
机译:在推定的胰岛素抵抗候选基因中,过氧化物酶体增殖物激活受体γ共激活因子1α(PGC-1α)是PPARγ和α的转录共激活因子,调节与能量产生和利用有关的多种过程,例如生热,肝糖异生,肌肉中葡萄糖的摄取。在人群研究中,据报道PGC-1α中的Gly482Ser替代与2型糖尿病和胰岛素抵抗的风险增加有关。在本研究中,我们分析了肥胖非糖尿病患者群体中PGC-1α基因的Gly482Ser错义突变与胰岛素敏感性和葡萄糖耐量之间的关联。通过PCR-RFLP在358名白种人肥胖受试者(223名葡萄糖耐量正常(NGT)和125名葡萄糖耐量受损(IGT))中检测到Gly482Ser SNP,我们观察到携带者之间存在显着相关性(p <0.007)。通过HOMAIR测定的PGC-1α基因的Gly482Ser变体和胰岛素抵抗多因素分析证实,Gly482Ser SNP是降低胰岛素敏感性的重要决定因素(p <0.02),独立于其他众所周知的胰岛素作用调节剂。我们发现肥胖受试者中PGC-1α基因的Gly482Ser变体与胰岛素敏感性降低之间存在显着关联,这种关联独立于所有其他已知的胰岛素抵抗调节剂,并提示PGC-1α基因在遗传上起主要作用肥胖患者对胰岛素抵抗的敏感性。

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