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GST T1、M1 和 IRS-1 G972R 基因变异与埃及女性妊娠期糖尿病(GDM)的关联:与母体高血糖相关。

GST T1, M1, and IRS-1 G972R Genetic Variants Association to Gestational Diabetes Mellitus (GDM) in Egyptian Women: Linkage to Maternal Hyperglycemia.

机构信息

Pediatric Department, Faculty of Medicine, Menoufia University, Shebin El-Kom, Egypt.

Department of Chemistry, Biochemistry Division, Faculty of Science, Al-Azhar University, Cairo, Egypt.

出版信息

Curr Diabetes Rev. 2022;18(2):e021921191604. doi: 10.2174/1573399817666210219124628.

Abstract

BACKGROUND

Gestational Diabetes Mellitus (GDM) shares in part the pathogenic mechanisms of multiple genetic interactions. Some of the T2D susceptibility genes are encountered in association with GDM.

OBJECTIVE

We aimed to investigate GST T1, M1, and G972R IRS-I gene polymorphisms with the risk of developing GDM.

METHODS

In this randomized case-control study, pregnant women with GDM were genotyped by PCR analysis for glutathione s-transferase-T1, M1 variant polymorphisms. RFLP was done for the G972R IRS 1 gene. Their newborns were additionally assayed for the whole of the clinical, laboratory, and genetic aspects.

RESULTS

The T allele IRS-1rs1801278 TT genotype was more frequently detected in GDM mothers in comparison to healthy control ones [for TT homozygous variant; OR(CI 95%): 2.05(1.09-3.87, p: 0.025)]. Furthermore, GST T1 null was significantly presented in GDM mothers than those of control mothers [OR (CI95%: 0.29 (0.084-1.02), p:0.04]. Added to the significant correlation of glycemic indices to clinical parameters of infants born to GDM, the M1-null genotype of GST was significantly correlated (p<0.05) to abnormal values of respiratory rates and 1 minute-APGAR score noted for extra NICU care.

CONCLUSION

Our results suggested that GST T1null and IRS-1 TT genotypic variants were claimed for GDM development among Egyptian women with a possible impact on their newly born infants.

摘要

背景

妊娠糖尿病(GDM)部分具有多种基因相互作用的致病机制。一些 2 型糖尿病易感性基因与 GDM 相关。

目的

我们旨在研究 GST T1、M1 和 G972R IRS-I 基因多态性与发生 GDM 的风险。

方法

在这项随机病例对照研究中,通过 PCR 分析对 GDM 孕妇的谷胱甘肽 S-转移酶 T1、M1 变体多态性进行基因分型。进行 RFLP 分析以检测 IRS-1 基因的 G972R。他们的新生儿还进行了全面的临床、实验室和遗传方面的检测。

结果

与健康对照组相比,GDM 母亲中 IRS-1rs1801278 TT 基因型的 T 等位基因更为常见[对于 TT 纯合变体;OR(95%CI):2.05(1.09-3.87,p:0.025)]。此外,GDM 母亲的 GST T1 缺失明显多于对照组母亲[OR(CI95%:0.29(0.084-1.02),p:0.04]。GDM 母亲的 GST M1 缺失基因型与新生儿血糖指数与临床参数呈显著相关性,新生儿呼吸频率和 1 分钟 APGAR 评分的异常值与需要额外 NICU 护理呈显著相关性(p<0.05)。

结论

我们的结果表明,GST T1null 和 IRS-1 TT 基因型变体在埃及女性中与 GDM 发展有关,可能对其新生儿有影响。

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