首页> 外文期刊>BMC Musculoskeletal Disorders >Association of IL-6 174G/C (rs1800795) and 572C/G (rs1800796) polymorphisms with risk of osteoporosis: a meta-analysis
【24h】

Association of IL-6 174G/C (rs1800795) and 572C/G (rs1800796) polymorphisms with risk of osteoporosis: a meta-analysis

机译:IL-6 174G / C(RS1800795)和572C / g(RS1800796)的关联,具有骨质疏松症风险的多态性:Meta分析

获取原文
       

摘要

Several studies have been performed to investigate association between IL-6 174G/C (rs1800795) and 572C/G (rs1800796) gene polymorphisms and osteoporosis predisposition. However, the results were conflicting. So, we performed a meta-analysis designed to provide more reliable results for the association between IL-6 gene polymorphisms and osteoporosis. Studies were searched using PubMed, EMBASE, the Cochrane Library and Wanfang electronic databases. The odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate the association between IL-6 174G/C (rs1800795) and 572C/G (rs1800796) gene polymorphisms and osteoporosis risk. The false-positive report probabilities (FPRP) test and the venice criteria were used to assess the credibility of statistically significant associations. A total of 9 studies with 1891 osteoporosis patients and 2027 healthy controls were included in current meta-analysis. Overall, The IL-6 174G/C (rs1800795) gene polymorphism was insignificantly associated with osteoporosis vulnerability. For IL-6 572C/G (rs1800796), statistically significant elevated osteoporosis vulnerability was found in IL-6 572C/G additive model (OR?=?2.25, 95% CI: 1.55–3.26), dominant model (OR?=?1.42, 95% CI: 0.78–2.56) and recessive model (OR?=?1.96, 95% CI: 1.36–2.83). However, the IL-6 572C/G C allele was found to be associated with reduced susceptibility to osteoporosis (OR?=?0.76, 95% CI: 0.56–1.04). When excluding studies that did not conform to HWE, the results did not change significantly. Further, when we evaluated the credibility of the positive results of the current meta-analysis, we identified less credible positive results in IL-6 572C/G recessive and additive model. In conclusion, IL-6 572C/G GG genotype may be associated with increased risk of osteoporosis.
机译:已经进行了几项研究以研究IL-6 174G / C(RS1800795)和572℃/ g(RS1800796)基因多态性和骨质疏松症易感性之间的关联。但是,结果是矛盾的。因此,我们进行了一个旨在为IL-6基因多态性和骨质疏松症之间的关联提供更可靠的结果。使用PubMed,Embase,Cochrane图书馆和Wanfang电子数据库搜索研究。计算了几率比(或)和95%置信区间(CIs)以评估IL-6 174g / C(RS1800795)和572℃/ g(RS1800796)基因多态性和骨质疏松症风险之间的关联。假阳性报告概率(FPRP)测试和威尼斯标准用于评估统计上重要协会的可信度。在目前的荟萃分析中,共有9项患有1891名骨质疏松症患者和2027例健康对照的研究。总的来说,IL-6 174G / C(RS1800795)基因多态性与骨质疏松症脆弱性无关紧要。对于IL-6 572C / g(RS1800796),在IL-6 572C / G添加剂模型中发现统计学显着的骨质疏松症脆弱性(或?=?2.25,95%CI:1.55-3.26),主导模型(或?=? 1.42,95%CI:0.78-2.56)和隐性模型(或?=?1.96,95%CI:1.36-2.83)。然而,发现IL-6 572C / G C等位基因与对骨质疏松症的易感性降低(或?= 0.76,95%CI:0.56-1.04)相关联。在排除没有符合HWE的研究时,结果并没有显着变化。此外,当我们评估当前荟萃分析的积极结果的可信度时,我们确定了IL-6 572C / G隐性和添加剂模型的不太可信的正面结果。总之,IL-6 572C / G GG基因型可能与骨质疏松症的风险增加有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号