Wu Haijing, Yu Ke, Yang Zhenghui
Department of Gynaecologic Oncology, Sichuan Cancer Hospital and Institute, No 55, Section 4 of Renmin South Road, Chengdu, 610041, Sichuan, People's Republic of China,
J Assist Reprod Genet. 2015 Apr;32(4):625-34. doi: 10.1007/s10815-015-0449-7. Epub 2015 Feb 18.
The associations between TNF-α and Interleukin gene polymorphisms and polycystic ovary syndrome (PCOS) risk have been studied in numerous epidemiological studies, but the results remain controversial. To investigate whether these polymorphisms facilitate susceptibility to PCOS, we conducted a comprehensive systematic review and meta-analysis.
PubMed, Embase, Web of Science, Medline, CNKI, and Google Scholar were searched to obtain the genetic association studies according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Odds ratios (OR) with corresponding 95 % confidence intervals (CI) were used to assess the strengths of the associations. Funnel plots and Egger's tests were performed to test for possible publication bias. All statistical analyses were performed using Review Manager 5.2 and STATA11.0.
Eighteen articles were included in the final meta-analysis. The studies involved the following polymorphisms: TNF-α -308G > A, TNF-α -805C>T, TNF-α -1031 T>C, IL-1A -889C>T, IL-1B -511C>T, IL-1B +3953 T>C, IL-6 -174G>C, IL-10 -819C>T, IL-10 -1082A>G, IL-18 -607C>A, and IL-18 -137G>C. Our results show a significant association between PCOS risk and the TNF-α -1031 T>C polymorphism (For TC+CC vs. TT: OR=2.09, 95 % CI=1.58-2.76, p<0.0001. For C allele vs. T allele: OR=1.67, 95 % CI=1.33-2.09, p<0.0001) and between PCOS risk and the IL-6 -174>C polymorphism (For CC+GC vs. GG: OR=0.49, 95 % CI=0.25-0.95, p=0.03. For CC vs. GG: OR=0.48, 95 % CI=0.28-0.80, p=0.005. For C vs. G: OR=0.60, 95 % CI=0.42-0.87, p=0.007). No associations were found with the other genetic models.
The results of the meta-analysis suggest positive associations between the TNF-α -1031 T>C and IL-6 -174G>C polymorphisms and the risk of PCOS. No associations are found between PCOS risk and the TNF-α -308G>A, TNF-α -805C>T, IL-1A -889C>T, IL-1B -511C>T, IL-1B +3953C>T, IL-10 -819C>T, IL-10 -1082 A>G, IL-18 -607C>A, and IL-18 -137G>C polymorphisms. However, due to the heterogeneity and low quality of the studies related to PCOS polymorphisms in the meta-analysis, the results should be interpreted with caution. Future multi-ethnicity studies of homogeneous populations of PCOS patients with larger sample sizes and well-matched controls are needed.
肿瘤坏死因子-α(TNF-α)和白细胞介素基因多态性与多囊卵巢综合征(PCOS)风险之间的关联已在众多流行病学研究中进行了探讨,但结果仍存在争议。为了研究这些多态性是否会增加PCOS易感性,我们进行了一项全面的系统评价和荟萃分析。
根据系统评价和荟萃分析的首选报告项目(PRISMA)指南,检索了PubMed、Embase、Web of Science、Medline、中国知网(CNKI)和谷歌学术,以获取基因关联研究。采用比值比(OR)及其相应的95%置信区间(CI)来评估关联强度。绘制漏斗图并进行Egger检验以检测可能的发表偏倚。所有统计分析均使用Review Manager 5.2和STATA11.0软件进行。
最终的荟萃分析纳入了18篇文章。这些研究涉及以下多态性:TNF-α -308G>A、TNF-α -805C>T、TNF-α -1031T>C、白细胞介素-1A(IL-1A)-889C>T、白细胞介素-1B(IL-1B)-511C>T、IL-1B +3953T>C、白细胞介素-6(IL-6)-174G>C、白细胞介素-10(IL-10)-819C>T、IL-10 -1082A>G、白细胞介素-18(IL-18)-607C>A和IL-18 -137G>C。我们的结果显示,PCOS风险与TNF-α -1031T>C多态性之间存在显著关联(TC+CC与TT相比:OR=2.09,95%CI=1.58-2.76,p<0.0001。C等位基因与T等位基因相比:OR=1.67,95%CI=1.33-2.09,p<0.0001),以及PCOS风险与IL-6 -174G>C多态性之间存在显著关联(CC+GC与GG相比:OR=0.49,95%CI=0.25-0.95,p=0.03。CC与GG相比:OR=0.48,95%CI=0.28-0.80,p=0.005。C与G相比:OR=0.60,95%CI=0.42-0.87,p=0.007)。在其他遗传模型中未发现关联。
荟萃分析结果提示,TNF-α -1031T>C和IL-6 -174G>C多态性与PCOS风险之间存在正相关。未发现PCOS风险与TNF-α -308G>A、TNF-α -805C>T、IL-1A -889C>T、IL-1B -511C>T、IL-1B +3953C>T、IL-10 -819C>T、IL-10 -1082A>G、IL-18 -607C>A和IL-18 -137G>C多态性之间存在关联。然而,由于荟萃分析中与PCOS多态性相关的研究存在异质性且质量较低,这些结果应谨慎解读。未来需要开展样本量更大、对照匹配良好的PCOS患者同质人群的多民族研究。