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增殖物激活受体γ Pro12Ala 与胰岛素受体底物 1 Gly972Arg 相互作用,增加南非混合人群发生胰岛素抵抗和糖尿病的风险。

Proliferator-activated receptor gamma Pro12Ala interacts with the insulin receptor substrate 1 Gly972Arg and increase the risk of insulin resistance and diabetes in the mixed ancestry population from South Africa.

机构信息

Biomedical Sciences, Faculty of Health and Wellness Sciences, Cape Peninsula University of Technology, PO Box 1906, Bellville 7530, Cape Town, South Africa.

出版信息

BMC Genet. 2014 Jan 21;15:10. doi: 10.1186/1471-2156-15-10.

Abstract

BACKGROUND

The peroxisome proliferator-activated receptor gamma (PPARG), Pro12Ala and the insulin receptor substrate (IRS1), Gly972Arg confer opposite effects on insulin resistance and type 2 diabetes mellitus (T2DM). We investigated the independent and joint effects of PPARG Pro12Ala and IRS1 Gly972Arg on markers of insulin resistance and T2DM in an African population with elevated risk of T2DM. In all 787 (176 men) mixed-ancestry adults from the Bellville-South community in Cape Town were genotyped for PPARG Pro12Ala and IRS1 Gly972Arg by two independent laboratories. Glucose tolerance status and insulin resistance/sensitivity were assessed.

RESULTS

Genotype frequencies were 10.4% (PPARG Pro12Ala) and 7.7% (IRS1 Gly972Arg). Alone, none of the polymorphisms predicted prevalent T2DM, but in regression models containing both alleles and their interaction term, PPARG Pro12 conferred a 64% higher risk of T2DM. Furthermore PPARG Pro12 was positively associated in adjusted linear regressions with increased 2-hour post-load insulin in non-diabetic but not in diabetic participants.

CONCLUSION

The PPARG Pro12 is associated with insulin resistance and this polymorphism interacts with IRS1 Gly972Arg, to increase the risk of T2DM in the mixed-ancestry population of South Africa. Our findings require replication in a larger study before any generalisation and possible application for risk stratification.

摘要

背景

过氧化物酶体增殖物激活受体 γ (PPARG)、脯氨酸 12 到丙氨酸 (Pro12Ala) 和胰岛素受体底物 (IRS1)、甘氨酸 972 到精氨酸 (Gly972Arg) 对胰岛素抵抗和 2 型糖尿病 (T2DM) 具有相反的影响。我们研究了在具有较高 T2DM 风险的非洲人群中,PPARG Pro12Ala 和 IRS1 Gly972Arg 对胰岛素抵抗和 T2DM 标志物的独立和联合作用。在开普敦贝尔维尔-南部社区的 787 名(176 名男性)混合血统成年人中,通过两个独立的实验室对 PPARG Pro12Ala 和 IRS1 Gly972Arg 进行了基因分型。评估了葡萄糖耐量状况和胰岛素抵抗/敏感性。

结果

基因型频率分别为 10.4%(PPARG Pro12Ala)和 7.7%(IRS1 Gly972Arg)。单独来看,这些多态性都不能预测 T2DM 的患病率,但在包含两个等位基因及其相互作用项的回归模型中,PPARG Pro12 使 T2DM 的风险增加了 64%。此外,在调整后的线性回归中,PPARG Pro12 与非糖尿病参与者餐后 2 小时胰岛素增加呈正相关,但在糖尿病参与者中则没有。

结论

PPARG Pro12 与胰岛素抵抗相关,该多态性与 IRS1 Gly972Arg 相互作用,增加了南非混合血统人群患 T2DM 的风险。在更大的研究中复制我们的发现后,才能进行推广,并有可能用于风险分层。

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