Tumor Necrosis Factor and Interleukin-6 Gene Polymorphisms and Endometriosis Risk in Asians: A Systematic Review and Meta-Analysis

IF 1.2 4区 生物学 Q4 GENETICS & HEREDITY Annals of Human Genetics Pub Date : 2013-12-06 DOI:10.1111/ahg.12048
Jie Li, Yang Chen, Shixiu Wei, Hongbo Wu, Chengjun Liu, Qiaoying Huang, Liuming Li, Yanling Hu
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引用次数: 14

Abstract

A relationship between endometriosis and tumor necrosis factor (TNF-α) and interleukin-6 (IL-6) gene polymorphisms has been raised for Asians. However, this topic is controversial. This study was a meta-analysis to explore whether TNF-α/IL-6 gene polymorphisms were associated with a risk of endometriosis in Asians. By searching PubMed, HuGENet, and China National Knowledge Infrastructure (CNKI) databases, 17 studies were identified and included (3372 cases and 4008 controls). The odds ratio (OR) with 95% confidence interval (CI) was used to assess the association between TNF-α/IL-6 gene polymorphisms and endometriosis risk. An association of TNF-α gene -1031T/C polymorphism with endometriosis was found (TT + TC vs. CC: OR 0.50, 95% CI 0.30–0.82, I2 = 37.1%, P = 0.20; TT vs. CC: OR 0.50, 95% CI 0.30–0.82, I2 = 43.0%, P = 0.173; TC vs. CC: OR 0.49, 95% CI 0.29–0.83, I2 = 10.6%, P = 0.327). In addition, TNF-α-238A/G and IL-6 -174C/G gene polymorphisms were also likely to be associated with endometriosis in Asians. For the TNF-α-238A/G gene polymorphism, the OR was 1.577 (95% CI: 1.01–2.48). For the IL-6 -174C/G gene polymorphism, the OR was 1.554 (95% CI: 1.04–2.31). No associations were detected between the TNF-α-308A/G and IL-6 -634C/G polymorphisms and susceptibility to endometriosis. Our results indicate that the TNF-α gene -1031T/C polymorphism can reduce the risk of endometriosis, but for Asians, TNF-α-238A/G and IL-6 -174C/G gene polymorphisms may be a risk factor for endometriosis. No association was found for the TNF-α-308A/G and IL-6 -634C/G gene polymorphisms.

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肿瘤坏死因子和白细胞介素-6基因多态性与亚洲人子宫内膜异位症的风险:系统回顾和荟萃分析
子宫内膜异位症与肿瘤坏死因子(TNF-α)和白细胞介素-6 (IL-6)基因多态性之间的关系已在亚洲人中提出。然而,这个话题是有争议的。本研究是一项荟萃分析,旨在探讨TNF-α/IL-6基因多态性是否与亚洲人子宫内膜异位症的风险相关。通过检索PubMed、HuGENet和中国知网数据库,共纳入17项研究(3372例,对照4008例)。采用95%可信区间(CI)的比值比(OR)评估TNF-α/IL-6基因多态性与子宫内膜异位症风险之间的关系。发现TNF-α基因-1031T/C多态性与子宫内膜异位症相关(TT + TC vs. CC: OR 0.50, 95% CI 0.30-0.82, I2 = 37.1%, P = 0.20;TT vs. CC: OR 0.50, 95% CI 0.30-0.82, I2 = 43.0%, P = 0.173;TC vs CC: OR 0.49, 95% CI 0.29-0.83, I2 = 10.6%, P = 0.327)。此外,TNF-α-238A/G和IL-6 -174C/G基因多态性也可能与亚洲人子宫内膜异位症有关。TNF-α-238A/G基因多态性OR为1.577 (95% CI: 1.01 ~ 2.48)。对于IL-6 -174C/G基因多态性,OR为1.554 (95% CI: 1.04-2.31)。TNF-α-308A/G、IL-6 -634C/G多态性与子宫内膜异位症易感性之间无相关性。本研究结果提示,TNF-α基因-1031T/C多态性可以降低子宫内膜异位症的风险,但对于亚洲人来说,TNF-α- 238a /G和IL-6 -174C/G基因多态性可能是子宫内膜异位症的危险因素。TNF-α-308A/G与il -634C/G基因多态性无相关性。
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来源期刊
Annals of Human Genetics
Annals of Human Genetics 生物-遗传学
CiteScore
4.20
自引率
0.00%
发文量
34
审稿时长
3 months
期刊介绍: Annals of Human Genetics publishes material directly concerned with human genetics or the application of scientific principles and techniques to any aspect of human inheritance. Papers that describe work on other species that may be relevant to human genetics will also be considered. Mathematical models should include examples of application to data where possible. Authors are welcome to submit Supporting Information, such as data sets or additional figures or tables, that will not be published in the print edition of the journal, but which will be viewable via the online edition and stored on the website.
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