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白细胞介素-18基因多态性与复发性流产风险:一项系统评价和荟萃分析。

Interleukin-18 gene polymorphisms and risk of recurrent pregnancy loss: A systematic review and meta-analysis.

作者信息

Chen Hui, Yang Xiaorong, Du Jinge, Lu Ming

机构信息

Clinical Epidemiology Unit, Qilu Hospital, Shandong University, Jinan, China.

Department of Epidemiology, School of Public Health, Shandong University, Jinan, China.

出版信息

J Obstet Gynaecol Res. 2015 Oct;41(10):1506-13. doi: 10.1111/jog.12800. Epub 2015 Sep 8.

Abstract

Interleukin-18 (IL-18) plays a potential pathological role in recurrent pregnancy loss (RPL). The results of published studies on the relationship between IL-18 gene promoter polymorphisms (-137G/C and-607C/A) and RPL risk remain controversial. This meta-analysis was performed to evaluate the association of IL-18, -137G/C and-607C/A gene polymorphisms with the risk of RPL under recessive, dominant and additive genetic models. A literature search was conducted in Medline, Embase and Web of Science for studies that described the effect of IL-18 gene polymorphisms on RPL risk. The numbers of each -137G/C and-607C/A genotype in the case and control groups were extracted. Quality of the original studies' methodology was also assessed. Meta-analysis was performed using Stata 13.1 software and the fixed effect model was used. Five articles were included in this meta-analysis. No significant heterogeneity between the studies was noted. The IL-18 -137 G/C polymorphism was significantly associated with an increased risk of RPL under a recessive genetic model (CC vs. GG + CG: odds ratio = 1.56, 95% confidence interval = 1.13 ~ 2.15). For the -607C/A mutation, we failed to find any association under any genetic models. The Egger's regression asymmetry test showed no publication bias. Our present study indicates a positive association between the CC genotype of the IL-18 -137G/C gene and RPL risk. Future well-designed large studies are needed to validate the association between IL-18 gene polymorphisms and the risk of RPL.

摘要

白细胞介素-18(IL-18)在复发性流产(RPL)中发挥着潜在的病理作用。已发表的关于IL-18基因启动子多态性(-137G/C和-607C/A)与RPL风险之间关系的研究结果仍存在争议。本荟萃分析旨在评估IL-18、-137G/C和-607C/A基因多态性在隐性、显性和加性遗传模型下与RPL风险的关联。在Medline、Embase和科学网中进行文献检索,以查找描述IL-18基因多态性对RPL风险影响的研究。提取病例组和对照组中每种-137G/C和-607C/A基因型的数量。还评估了原始研究方法的质量。使用Stata 13.1软件进行荟萃分析,并采用固定效应模型。本荟萃分析纳入了五篇文章。各研究之间未发现显著异质性。在隐性遗传模型下,IL-18 -137 G/C多态性与RPL风险增加显著相关(CC与GG + CG相比:比值比 = 1.56,95%置信区间 = 1.13 ~ 2.15)。对于-607C/A突变,我们在任何遗传模型下均未发现任何关联。Egger回归不对称检验未显示发表偏倚。我们目前的研究表明,IL-18 -137G/C基因的CC基因型与RPL风险呈正相关。未来需要设计良好的大型研究来验证IL-18基因多态性与RPL风险之间的关联。

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