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中国孕妇中微小RNA结合位点变异与妊娠期糖尿病风险的研究。

Investigation of miRNA-binding site variants and risk of gestational diabetes mellitus in Chinese pregnant women.

作者信息

Wang Xiaojing, Li Wei, Ma Liangkun, Ping Fan, Liu Juntao, Wu Xueyan, Mao Jiangfeng, Wang Xi, Nie Min

机构信息

Key Laboratory of Endocrinology, Ministry of Health, Department of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Shuai fu Yuan No. 1, Dongcheng District, Beijing, 100730, China.

Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, 100730, China.

出版信息

Acta Diabetol. 2017 Mar;54(3):309-316. doi: 10.1007/s00592-017-0969-y. Epub 2017 Feb 11.

Abstract

AIMS

Emerging evidence suggested genetic factor attributed as a major determinant for the complex pathogenic mechanism of gestational diabetes mellitus (GDM), but the related genetic study was limited. We aimed to investigate the impact of polymorphisms in miRNA-binding sites (miR-binding SNPs) on the risk of GDM in Chinese Han pregnant women.

METHODS

We screened GDM susceptibility genes extensively and selected miR-binding SNPs using four bioinformatics software. TaqMan allelic discrimination assays were applied to miR-binding SNPs genotyping in 839 GDM patients and 900 controls.

RESULTS

In total five potential miR-binding SNPs (SLC30A8 rs2466293, INSR rs1366600, INSR rs3745550, KCNJ11 rs5210 and KCNQ1 rs8234) were selected. Our results showed that SLC30A8 rs2466293 [OR 95% CI = 1.455 (1.077, 1.966); P = 0.014] and INSR rs1366600 [OR 95% CI = 2.191 (1.077, 4.455); P = 0.029] increased the risk of GDM after adjusting age in additive model. Furthermore, rs2466293 was found to significantly associate with higher levels of fasting plasma glucose (b  = 0.054, P  = 0.032), 2-h OGTT plasma glucose (b  = 0.069, P  = 0.007), lower fasting insulin concentrations (b  = -0.082, P  = 0.003) and decreased HOMA-B (b  = -0.067, P  = 0.015). Additionally, the correlation between rs1366600 and 2-h OGTT plasma glucose (b  = 0.078, P  = 0.001) was observed.

CONCLUSIONS

Two miR-binding SNPs SLC30A8 rs2466293 and INSR rs1366600 increased GDM susceptibility. Functional studies were required to confirm the underlying mechanism. Our study provided additional insights into the genetic pathogenesis of GDM.

摘要

目的

新出现的证据表明,遗传因素是妊娠期糖尿病(GDM)复杂致病机制的主要决定因素,但相关的遗传学研究有限。我们旨在研究微小RNA结合位点多态性(miR结合单核苷酸多态性,miR-binding SNPs)对中国汉族孕妇患GDM风险的影响。

方法

我们广泛筛选GDM易感基因,并使用四种生物信息学软件选择miR结合单核苷酸多态性。采用TaqMan等位基因鉴别分析对839例GDM患者和900例对照进行miR结合单核苷酸多态性基因分型。

结果

共选择了5个潜在的miR结合单核苷酸多态性(SLC30A8 rs2466293、INSR rs1366600、INSR rs3745550、KCNJ11 rs5210和KCNQ1 rs8234)。我们的结果显示,在年龄校正后的加性模型中,SLC30A8 rs2466293 [比值比(OR)95%置信区间(CI)=1.455(1.077,1.966);P=0.014]和INSR rs1366600 [OR 95% CI=2.191(1.077,4.455);P=0.029]增加了GDM的风险。此外,发现rs2466293与较高的空腹血糖水平显著相关(b=0.054,P=0.032)、口服葡萄糖耐量试验2小时血糖水平(b=0.069,P=0.007)、较低的空腹胰岛素浓度(b=-0.082,P=0.003)以及较低的胰岛素抵抗指数(HOMA-B)(b=-0.067,P=0.015)。此外,还观察到rs1366600与口服葡萄糖耐量试验2小时血糖水平之间的相关性(b=0.078,P=0.001)。

结论

两个miR结合单核苷酸多态性SLC30A8 rs2466293和INSR rs1366600增加了GDM易感性。需要进行功能研究以证实潜在机制。我们的研究为GDM的遗传发病机制提供了更多见解。

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