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IGF2BP2 基因变异与 2 型糖尿病风险的定量评估。

Quantitative assessment of the variation in IGF2BP2 gene and type 2 diabetes risk.

机构信息

Department of Endocrinology, Changhai Hospital of Shanghai, Second Military Medical University, Shanghai 200433, People's Republic of China.

出版信息

Acta Diabetol. 2012 Dec;49 Suppl 1:S87-97. doi: 10.1007/s00592-011-0336-3. Epub 2011 Oct 21.

DOI:10.1007/s00592-011-0336-3
PMID:22015911
Abstract

Insulin-like growth factor 2 mRNA-binding protein 2 (IFG2BP2) belongs to an mRNA-binding protein family involved in the development and stimulation of insulin action, which has attracted considerable attention as a candidate gene for type 2 diabetes (T2D) since it was first identified through genome-wide association approach. The relationship between IFG2BP2 and T2D has been reported in various ethnic groups; however, these studies have yielded contradictory results. To investigate this inconsistency, we performed a meta-analysis of 35 studies involving a total of 175,965 subjects for two wildly studied polymorphisms (rs4402960 and rs1470579) of the IFG2BP2 to evaluate the effect of IFG2BP2 on genetic susceptibility for T2D. An overall random-effects per-allele OR of 1.13 (95% CI: 1.12-1.15; P < 10(-5)) and 1.09 (95% CI: 1.07-1.12; P < 10(-5)) was found for the two variants, respectively. Significant results were also observed using dominant or recessive genetic model. No significant results between study heterogeneity were found in most of the comparison. In the subgroup analysis by ethnicity, sample size, diagnostic criterion and mean age and BMI of cases, significantly increased risks were found for these polymorphisms in almost all genetic models. This meta-analysis demonstrated that these two common polymorphisms is a risk factor for developing T2D, but these associations vary in different ethnic populations.

摘要

胰岛素样生长因子 2 mRNA 结合蛋白 2(IFG2BP2)属于一种 mRNA 结合蛋白家族,参与胰岛素作用的发育和刺激,自通过全基因组关联方法首次鉴定以来,它作为 2 型糖尿病(T2D)的候选基因引起了相当大的关注。IFG2BP2 与 T2D 之间的关系在不同种族中均有报道;然而,这些研究的结果存在矛盾。为了研究这种不一致性,我们对 35 项研究进行了荟萃分析,这些研究共涉及 175965 名受试者,对 IFG2BP2 的两个广泛研究的多态性(rs4402960 和 rs1470579)进行了评估,以评估 IFG2BP2 对 T2D 的遗传易感性的影响。对这两种变体的总体随机效应每等位基因 OR 分别为 1.13(95%CI:1.12-1.15;P < 10(-5))和 1.09(95%CI:1.07-1.12;P < 10(-5))。使用显性或隐性遗传模型也观察到了显著结果。在大多数比较中,研究异质性之间没有发现显著结果。按种族、样本量、诊断标准和病例的平均年龄和 BMI 进行亚组分析,在几乎所有遗传模型中,这些多态性都发现了明显的风险增加。这项荟萃分析表明,这两种常见的多态性是发生 T2D 的危险因素,但这些关联在不同的种族群体中有所不同。

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