首页> 外文期刊>Human Genetics >Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate
【24h】

Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate

机译:IRF6基因与母亲的多种维生素的基因-环境相互作用在控制有/无c裂的唇裂风险中的证据

获取原文
获取原文并翻译 | 示例
           

摘要

Although multiple genes have been identified as genetic risk factors for isolated, non-syndromic cleft lip with/without cleft palate (CL/P), a complex and heterogeneous birth defect, interferon regulatory factor 6 gene (IRF6) is one of the best documented genetic risk factors. In this study, we tested for association between markers in IRF6 and CL/P in 326 Chinese case–parent trios, considering gene–environment interaction for two common maternal exposures, and parent-of-origin effects. CL/P case–parent trios from three sites in mainland China and Taiwan were genotyped for 22 single nucleotide polymorphisms (SNPs) in IRF6. The transmission disequilibrium test was used to test for marginal effects of individual SNPs. We used PBAT to screen the SNPs and haplotypes for gene–environment (G × E) interaction and conditional logistic regression models to quantify effect sizes for SNP–environment interaction. After Bonferroni correction, 14 SNPs showed statistically significant association with CL/P. Evidence of G × E interaction was found for both maternal exposures, multivitamin supplementation and environmental tobacco smoke (ETS). Two SNPs showed evidence of interaction with multivitamin supplementation in conditional logistic regression models (rs2076153 nominal P = 0.019, rs17015218 nominal P = 0.012). In addition, rs1044516 yielded evidence for interaction with maternal ETS (nominal P = 0.041). Haplotype analysis using PBAT also suggested interaction between SNPs in IRF6 and both multivitamin supplementation and ETS. However, no evidence for maternal genotypic effects or significant parent-of-origin effects was seen in these data. These results suggest IRF6 gene may influence risk of CL/P through interaction with multivitamin supplementation and ETS in the Chinese population.
机译:尽管已鉴定出多种基因作为分离的,非综合症的left裂伴或不伴left裂(CL / P),复杂而异质的先天性缺陷的遗传危险因素,但干扰素调节因子6基因(IRF6)是最有据可查的基因之一遗传危险因素。在这项研究中,我们考虑了两种常见母体暴露的基因-环境相互作用以及原产地效应,测试了326个中国病例-父母三重奏中IRF6和CL / P标记之间的关联。对来自中国大陆和台湾三个地点的CL / P病例-父母三重基因组进行了IRF6中22个单核苷酸多态性(SNP)的基因分型。传输不平衡测试用于测试单个SNP的边际效应。我们使用PBAT筛选了基因与环境(G×E)相互作用的SNP和单倍型,并使用条件对数回归模型来量化SNP与环境相互作用的效应大小。 Bonferroni校正后,有14个SNPs与CL / P具有统计学意义的关联。孕产妇接触,补充多种维生素和环境烟草烟雾(ETS)均发现G×E相互作用。在条件对数回归模型中,两个SNP显示出与多种维生素补充剂相互作用的证据(rs2076153标称P = 0.019,rs17015218标称P = 0.012)。此外,rs1044516还提供了与母体ETS相互作用的证据(标称P = 0.041)。使用PBAT进行单倍型分析还表明,IRF6中的SNP与多种维生素补充剂和ETS之间存在相互作用。但是,在这些数据中没有发现母亲基因型效应或显着的起源母体效应的证据。这些结果表明,IRF6基因可能通过与多种维生素补充剂和ETS相互作用而影响中国人群的CL / P风险。

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