首页> 美国卫生研究院文献>PLoS Clinical Trials >Association Analysis of Single Nucleotide Polymorphisms at Five Loci: Comparison between Atopic Dermatitis and Asthma in the Chinese Han Population
【2h】

Association Analysis of Single Nucleotide Polymorphisms at Five Loci: Comparison between Atopic Dermatitis and Asthma in the Chinese Han Population

机译:五个位点单核苷酸多态性的关联分析:中国汉族人群特应性皮炎和哮喘的比较

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Atopic diseases, such as atopic dermatitis (AD) and asthma, are closely related to clinical phenotypes with hypersensitivity, and often share some similar genetic and pathogenic bases. Our recent GWAS identified three susceptibility gene/loci FLG (rs11204971 and rs3126085), 5q22.1 (rs10067777, rs7701890, rs13360927 and rs13361382) and 20q13.33 (rs6010620) to AD. The effect of these AD associated polymorphisms in asthma is so far unknown. To investigate whether AD relevant genetic variants is identical to asthma and reveal the differences in genetic factors between AD and asthma in Chinese Han population, seven AD associated single nucleotide polymorphisms (SNPs) as well as 3 other SNPs (rs7936562 and rs7124842 at 11q13.5 and rs4982958 at 14q11.2) from our previous AD GWAS were genotyped in 463 asthma patients and 985 controls using Sequenom MassArray system. We found rs4982958 at 14q11.2 was significantly associated with asthma (P = 3.04×10−4, OR = 0.73). We also detected one significant risk haplotype GGGA from the 4 SNPs (rs10067777, rs7701890, rs13360927 and rs13361382) at 5q22.1 in AD cases (P correction = 3.60×10−10, OR = 1.26), and the haplotype was suggestive of risk in asthma cases in this study (P = 0.014, P correction = 0.084, OR = 1.38). These SNPs (rs11204971, rs3126085, rs7936562, rs712484 and rs6010620) at AD susceptibility genes/loci FLG, 11q13.5 and 20q13.33 were not associated with asthma in this study. Our results further comfirmed that 14q11.2 was an important candidate locus for asthma and demonstrated that 5q22.1 might be shared by AD and asthma in Chinese Han population.
机译:特应性疾病,例如特应性皮炎(AD)和哮喘,与临床表型过敏相关,并且经常具有一些相似的遗传和致病基础。我们最近的GWAS确定了对AD的三个易感基因/基因座FLG(rs11204971和rs3126085),5q22.1(rs10067777,rs7701890,rs13360927和rs13361382)和20q13.33(rs6010620)。迄今为止,这些与AD相关的多态性在哮喘中的作用尚不清楚。为了调查AD相关遗传变异是否与哮喘相同,并揭示中国汉族人群AD与哮喘之间的遗传因素差异,七个与AD相关的单核苷酸多态性(SNP)和三个其他SNP(在11q13.5时为rs7936562和rs7124842)和来自我们先前AD GWAS的rs4982958(14q11.2)的基因型使用Sequenom MassArray系统对463名哮喘患者和985名对照进行了基因分型。我们发现14q11.2处的rs4982958与哮喘显着相关(P = 3.04×10 -4 ,OR = 0.73)。在AD病例中,我们在5q22.1时从4个SNP(rs10067777,rs7701890,rs13360927和rs13361382)中检测到一个显着风险单倍型GGGA(P校正= 3.60×10 -10 ,OR = 1.26),在这项研究中,单倍型提示有哮喘病风险(P = 0.014,P校正= 0.084,OR = 1.38)。在本研究中,AD易感基因/位置FLG,11q13.5和20q13.33的这些SNP(rs11204971,rs3126085,rs7936562,rs712484和rs6010620)与哮喘无关。我们的结果进一步证实14q11.2是哮喘的重要候选位点,并证明5q22.1可能与AD和哮喘在中国汉族人群中共享。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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