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常见的信号转导和转录激活因子3(STAT3)变体与女性双胞胎的肥胖或胰岛素抵抗无关。

Common STAT3 variants are not associated with obesity or insulin resistance in female twins.

作者信息

Jamshidi Yalda, Kyriakou Theodosios, Gooljar Sakina B, Collins Laura J, Lane Carl A, Snieder Harold, Wang Xiaoling, Spector Tim D, O'Dell Sandra D

机构信息

Nutrition Food and Health Research Centre, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH, United Kingdom.

出版信息

Obesity (Silver Spring). 2007 Jul;15(7):1634-9. doi: 10.1038/oby.2007.194.

Abstract

In animal models, STAT3 action in the hypothalamus and liver appears essential for normal body weight and glucose homeostasis in response to insulin. We hypothesized that variation in the STAT3 gene may be associated with body fat and/or insulin resistance in the general population. Five tagging SNPs spanning the STAT3 gene, rs8074524, rs2293152, rs2306580, rs6503695, and rs7211777 were genotyped in 2776 white female twins (mean age, 47.4+/-12.5 yrs) from the St Thomas' United Kingdom Adult Twin Registry (Twins UK). Minor allele frequencies were as follows: rs8074524 (0.19), rs2293152 (0.37), rs2306580 (0.06), rs6503695 (0.35), and rs7211777 (0.34). The minor allele of rs2293152 was associated with higher homeostasis model assessment index of insulin resistance (p=0.013) in the full cohort and confirmed in sib-transmission/disequilibrium test (TDT): (p=0.015; n=60). However, there were no associations with fasting serum insulin or glucose or with obesity variables. Although defective STAT3 action results in obesity and insulin resistance in animal models, we failed to establish any indicative associations with common SNPs in this human study.

摘要

在动物模型中,下丘脑和肝脏中的信号转导及转录激活因子3(STAT3)的作用对于响应胰岛素时的正常体重和葡萄糖稳态似乎至关重要。我们推测,STAT3基因的变异可能与普通人群的体脂和/或胰岛素抵抗有关。对来自英国圣托马斯成人双胞胎登记处(Twins UK)的2776名白人女性双胞胎(平均年龄47.4±12.5岁)进行了跨越STAT3基因的5个标签单核苷酸多态性(SNP)的基因分型,这些SNP分别为rs8074524、rs2293152、rs2306580、rs6503695和rs7211777。次要等位基因频率如下:rs8074524(0.19)、rs2293152(0.37)、rs2306580(0.06)、rs6503695(0.35)和rs7211777(0.34)。rs2293152的次要等位基因与整个队列中较高的胰岛素抵抗稳态模型评估指数相关(p = 0.013),并在同胞传递/不平衡检验(TDT)中得到证实:(p = 0.015;n = 60)。然而,与空腹血清胰岛素或葡萄糖以及肥胖变量均无关联。尽管在动物模型中STAT3功能缺陷会导致肥胖和胰岛素抵抗,但在这项人体研究中,我们未能确定与常见SNP有任何指示性关联。

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