IRF6 rs2235371多态性与非综合征性唇腭裂的关联:一项meta分析

H. Neamatzadeh, M. Zare-Shehneh, M. Mazaheri, K. Daliri, E. Akbarian, E. Sheikhpour
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引用次数: 0

摘要

背景:先前发表的关于干扰素调节因子6 (IRF6)多态性与非综合征性唇腭裂(NSCL±P)风险之间关系的数据仍然没有定论。本研究的目的是进行一项荟萃分析,以进一步评估这些关联。方法:综合检索PubMed、EMBASE、Web of Science和CNKI,检索截至2021年7月的所有符合条件的研究。结果:本次荟萃分析共纳入23项研究,6161例病例和8919例对照。综合分析表明,在等位基因(a对G: OR=0.754, 95% CI 0.628 ~ 0.905, P=0.002)、纯合子(AA对GG: OR=0.621, 95% CI 0.405 ~ 0.953, P=0.029)、杂合子(AC对GG: OR=0.619, 95% CI 0.485 ~ 0.791, P≤0.001)、显性(AA+AG对GG: OR=0.550, 95% CI 0.381 ~ 0.794, P=0.001)和隐性模型(AA对AG+GG: OR=0.583, 95% CI 0.423 ~ 0.804, P=0.001)下,IRF6 rs2235371多态性与CL±P风险均存在显著相关性。种族亚组分析显示,rs2235371与亚洲人的NSCL±P风险相关。结论:本荟萃分析提供了强有力的证据,证明IRF6 rs2235371可能与nsl±P的风险相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of IRF6 rs2235371 Polymorphism with Non-Syndromic Cleft Lip/Palate: A Meta-analysis
Background: The previous published data on the association between interferon regulatory factor 6 (IRF6) polymorphisms and non-syndromic Cleft Lip/Palate (NSCL ± P) risk remained inconclusive. The aim of this study was to conduct a meta-analysis to further assess the associations. Methods: A comprehensive search in PubMed, EMBASE, Web of Science, and CNKI for all eligible studies up July 2021. Results: A total of 23 studies with 6,161 cases and 8,919 controls were selected for this meta-analysis. Overall pooled analysis suggest a significant association between IRF6 rs2235371 polymorphism and CL±P risk under all the five genetic models, i.e., allele (A vs. G: OR=0.754, 95% CI 0.628-0.905, P=0.002), homozygote (AA vs. GG: OR=0.621 95% 0.405-0.953, P=0.029), heterozygote (AC vs. GG: OR=0.619, 95% CI 0.485-0.791, P≤0.001), dominant (AA+AG vs. GG: OR=0.550, 95% CI 0.381-0.794, P=0.001) and recessive model (AA vs. AG+GG: OR=0.583, 95% CI 0.423-0.804, P=0.001). Subgroup analysis by ethnicity showed that rs2235371 was associated with NSCL±P risk in Asians. Conclusion: This meta-analysis provides strong evidences that IRF6 rs2235371 might be associated with risk of NSCL ± P.
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