Chen Hui, Yang Xiaorong, Du Jinge, Lu Ming
Clinical Epidemiology Unit, Qilu Hospital, Shandong University, Jinan, China.
Department of Epidemiology, School of Public Health, Shandong University, Jinan, China.
J Obstet Gynaecol Res. 2015 Oct;41(10):1506-13. doi: 10.1111/jog.12800. Epub 2015 Sep 8.
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.
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。