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在法裔加拿大家庭样本中17q21单核苷酸多态性与哮喘之间关联的重复研究。

Replication of an association between 17q21 SNPs and asthma in a French-Canadian familial collection.

作者信息

Madore Anne-Marie, Tremblay Karine, Hudson Thomas J, Laprise Catherine

机构信息

Department of Medicine, Laval University, Laval, QC, Canada.

出版信息

Hum Genet. 2008 Feb;123(1):93-5. doi: 10.1007/s00439-007-0444-x. Epub 2007 Nov 9.

Abstract

Asthma is a complex trait which is influenced by environmental and genetic factors. In a recent genome-wide association study on asthma in European subjects, novel associations were reported between 17q21 single nucleotide polymorphisms (SNPs) and childhood asthma. We performed an association study with the ten SNPs that showed the strongest association in a French-Canadian asthmatic familial collection. Family-based association tests revealed significant associations for eight SNPs (0.005 < P < 0.017) and for two haplotypes (P = 0.0004 and 0.002), confirming the 17q21 as an asthma locus.

摘要

哮喘是一种受环境和遗传因素影响的复杂性状。在最近一项针对欧洲受试者哮喘的全基因组关联研究中,报告了17q21单核苷酸多态性(SNP)与儿童哮喘之间的新关联。我们对在法裔加拿大哮喘家族样本中显示出最强关联的10个SNP进行了关联研究。基于家系的关联检验显示,8个SNP(0.005 < P < 0.017)和2个单倍型(P = 0.0004和0.002)存在显著关联,证实17q21为哮喘相关基因座。

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