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首页> 外文期刊>Archives of Oral Biology >Association between the IRF6 rs2235371 polymorphism and the risk of nonsyndromic cleft lip with or without cleft palate in Chinese Han populations: A meta-analysis
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Association between the IRF6 rs2235371 polymorphism and the risk of nonsyndromic cleft lip with or without cleft palate in Chinese Han populations: A meta-analysis

机译:IRF6 rs2235371多态性与中国汉族人群中有或没有腭裂的非肌肉裂隙唇的关联:META分析

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Highlights ? The IRF6 rs2235371 T allele decreased the risk of NSCL/P in Chinese Han populations. ? The variant T allele significantly decreased the risk of CLO and CLP, but not for CPO. ? The variant T allele decreased the risk of NSCL/P in Northern Chinese populations. ? Only two genetic models support that the variant T allele decreased the risk of NSCL/P in Southern Chinese populations. Abstract Objective To investigate the association between the risk of nonsyndromic cleft lip with or without cleft palate (NSCL/P) and the IRF6 rs2235371 (C>T) polymorphism in Chinese Han populations. Design PubMed, Web of Science and EMBASE were searched through May 31, 2016, to select eligible studies. Pooled odds ratios (ORs) with 95% confidence intervals (95% CIs) were applied to estimate the risk of NSCL/P associated with the IRF6 rs2235371 polymorphism. Subgroup analyses were conducted according to NSCL/P types (CLO, CPO and CLP) and the geographical location (Northern China and Southern China). Publication bias and sensitivity analyses were performed to assess the reliability of the results. Results A total of 1275 NSCL/P cases and 1294 controls from seven eligible case-control studies were included. In the overall analysis, a significant association between the IRF6 rs2235371 polymorphism and the risk of NSCL/P was identified under all genetic models, with the exception of the recessive model (T vs. C: OR=0.68, 95%CI=0.60-0.76, P Conclusions The IRF6 rs2235371 T allele decreased the risk of NSCL/P in Chinese Han populations. However, further studies with large sample sizes should be conducted to confirm this association.
机译:强调 ? IRF6 RS2235371 T等位基因降低了中国汉族人群NSCL / P的风险。还变体T等位基因显着降低了CLO和CLP的风险,但不是CPO。还变体T等位基因降低了北方人口中NSCL / P的风险。还只有两个遗传模型支持,变异性吨等位基因在南方群体中降低了NSCL / P的风险。摘要目的探讨无论腭裂(NSCL / P)和中国汉族人群的IRF6 RS2235371(C> T)多态性的非肌肉裂隙唇风险与中国汉族人群的多态性。 2016年5月31日,搜查了PubMed,科学网络和Embase网,选择合格的研究。汇总的差距(ORS)具有95%置信区间(95%CIs)来估计与IRF6 RS2235371多态性相关的NSCL / P的风险。根据NSCL / P类型(CLO,CPO和CLP)和地理位置(中国北部和中国北部)进行亚组分析。进行出版物偏差和敏感性分析以评估结果的可靠性。结果包括共有1275个NSCL / P案例和来自七项合格案件控制研究的1294个控制。在整体分析中,在所有遗传模型中鉴定了IRF6 RS2235371多态性和NSCL / P之间的风险之间的重要关联,除了隐性模型(T VS.C:OR = 0.68,95%CI = 0.60- 0.76,P结论IRF6 RS2235371 T等位基因降低了中国汉族人群中NSCL / P的风险。但是,应进行大型样本尺寸的进一步研究以确认该协会。

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