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FOXP3 基因多态性对子痫前期发病风险的影响:Meta 分析及生物信息学方法

Influence of FOXP3 gene polymorphisms on the risk of preeclampsia: a meta-analysis and a bioinformatic approach.

机构信息

Department of Molecular and Cell Biology, Faculty of Basic Sciences, University of Mazandaran, Babolsar, Iran.

Department of Cell and Molecular Biology, Kosar University of Bojnord, Bojnord, Iran.

出版信息

Clin Exp Hypertens. 2022 Apr 3;44(3):280-290. doi: 10.1080/10641963.2021.2022685. Epub 2022 Jan 11.

Abstract

BACKGROUND AND AIM

Preeclampsia (PE), a multifactorial disorder, is the main cause of maternal mortality and morbidity. Genetic polymorphisms in key proteins involved in the immune system may change the risk of PE risk. In this study, we examined the association of two rs2232365 and rs3761548 common polymorphisms of the FOXP3 immune response gene with PE susceptibility by a meta-analysis which was followed by an in-silico analysis.

MATERIALS AND METHODS

Through a systematic search in databases including PubMed, MEDLINE, Google Scholar, and Science Direct, we find eligible studies for meta-analysis. Some bioinformatics tools were used to detect the impact of rs2232365 and rs3761548 polymorphisms on the FOXP3 gene function.

RESULTS

Our data revealed that there is a significant association between rs3761548 polymorphism and decreased risk of PE. In addition, we observed a significant association between rs2232365 and increased risk of mild preeclampsia. Also, our bioinformatic analysis showed that both rs2232365 and rs3761548 polymorphisms could affect FOXP3 gene function.

CONCLUSION

Based on our findings, the rs3761548 genetic variation could be a protective factor against PE risk. While the rs2232365 polymorphism may be a genetic risk factor for mild preeclampsia. Therefore, as a preliminary study, these genetic variations could be considered molecular biomarkers for PE disorder.

摘要

背景与目的

子痫前期(PE)是一种多因素疾病,是孕产妇死亡和发病的主要原因。参与免疫系统的关键蛋白的遗传多态性可能会改变 PE 风险。在这项研究中,我们通过荟萃分析研究了 FOXP3 免疫反应基因的两个常见 rs2232365 和 rs3761548 多态性与 PE 易感性的关系,随后进行了计算机分析。

材料与方法

通过在包括 PubMed、MEDLINE、Google Scholar 和 Science Direct 在内的数据库中进行系统搜索,我们找到了用于荟萃分析的合格研究。使用了一些生物信息学工具来检测 rs2232365 和 rs3761548 多态性对 FOXP3 基因功能的影响。

结果

我们的数据表明,rs3761548 多态性与 PE 风险降低之间存在显著关联。此外,我们观察到 rs2232365 与轻度子痫前期风险增加之间存在显著关联。此外,我们的生物信息学分析表明,rs2232365 和 rs3761548 多态性都可能影响 FOXP3 基因功能。

结论

基于我们的发现,rs3761548 遗传变异可能是 PE 风险的保护因素。而 rs2232365 多态性可能是轻度子痫前期的遗传风险因素。因此,作为初步研究,这些遗传变异可以被视为 PE 障碍的分子生物标志物。

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