...
首页> 外文期刊>The Cleft palate-craniofacial journal: official publication of the American Cleft Palate-Craniofacial Association >Genetic effect of transforming growth factor alpha gene variants on the risk of nonsyndromic cleft lip with or without palate in Korean populations
【24h】

Genetic effect of transforming growth factor alpha gene variants on the risk of nonsyndromic cleft lip with or without palate in Korean populations

机译:转化生长因子α基因变异对韩国人群上颚或非上颚非综合征性唇裂风险的遗传效应

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: To identify the contribution of TGFA gene variants to the risk of nonsyndromic cleft lip with or without palate (NS-CL±P). Design: The samples were from 142 Korean NS-CL±P families and 119 control parents having nonaffected children. Minor allele frequency, heterozygosity, and χ2 test for Hardy-Weinberg equilibrium were calculated for each of 10 selected single-nucleotide polymorphisms (SNPs). Ten SNPs were used to examine the association of case-parent trios with the transmission disequilibrium test (TDT) and conditional logistic regression models (CLRMs). Both allelic and genotypic TDTs for individual SNPs and sliding windows of haplotypes consisting of two to five SNPs were tested using family- and haplotype-based association test programs. Genotypic odd ratios (GORs) were obtained from CLRMs using STATA software. The parent-of-origin effect was evaluated for 10 SNPs, and a comparison between 218 case parents and 119 control parents was performed to investigate paternal and maternal ORs. Results: Family-based TDT and haplotype analysis exhibited no statistical significance, but a relatively meaningful association was shown with rs3771497 (all P < .05; two SNPs, rs3771497 and rs3755377; five SNPs, rs3771497, rs3755377, rs3771485, rs11466212, and rs3771475). G/G homozygotes at rs3771497 have a significant decreased risk of NS-CL±P (GOR = 0.30, P < .01). No SNPs showed parent-of-origin effects. However, in the comparison between case parents and control parents, a single-marker analysis of maternal line showed a significant association with NS-CL±P in rs3771497 (P < .001, recessive model). Conclusion: The association of the TGFA gene with NS-CL±P in Korean populations was not clearly found. However, the etiologic effect of the TGFA gene on NS-CL±P patients should be investigated in terms of maternal genotype influence.
机译:目的:确定TGFA基因变异对有或没有pa(NS-CL±P)的非综合征性唇裂风险的影响。设计:样本来自142个韩国NS-CL±P家庭和119个有未患病子女的对照父母。针对所选的10个单核苷酸多态性(SNP)中的每一个,计算了次要等位基因频率,杂合性和Hardy-Weinberg平衡的χ2检验。使用十个SNP来检查病例父母三重奏与传输不平衡检验(TDT)和条件逻辑回归模型(CLRM)的关联。使用基于家族和单倍型的关联测试程序测试了单个SNP的等位基因TDT和基因型TDT,以及由2至5个SNP组成的单倍型滑动窗。使用STATA软件从CLRM获得基因型奇数比(GOR)。评估了10个SNP的原产父母效应,并比较了218例父母和119例对照父母,以调查父亲和母亲的OR。结果:基于家族的TDT和单倍型分析没有统计学意义,但与rs3771497呈现相对有意义的关联(所有P <.05;两个SNP,rs3771497和rs3755377;五个SNP,rs3771497,rs3755377,rs3771485,rs11466212和rs3771475 )。 rs3771497的G / G纯合子的NS-CL±P风险显着降低(GOR = 0.30,P <.01)。没有SNPs显示出原产地的影响。然而,在案例父母与对照父母之间的比较中,对母系的单标记分析显示rs3771497中与NS-CL±P有显着关联(P <.001,隐性模型)。结论:韩国人群中TGFA基因与NS-CL±P的相关性尚不清楚。但是,应根据母体基因型的影响研究TGFA基因对NS-CL±P患者的病因学影响。

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