Tsai Hui-Ju, Shaikh Nishat, Kho Jennifer Y, Battle Natalie, Naqvi Mariam, Navarro Daniel, Matallana Henry, Lilly Craig M, Eng Celeste S, Kumar Gunjan, Thyne Shannon, Watson H George, Meade Kelley, LeNoir Michael, Choudhry Shweta, Burchard Esteban G
Department of Medicine, University of California, San Francisco, CA 94143-0833, USA.
Hum Genet. 2006 Jun;119(5):547-57. doi: 10.1007/s00439-006-0169-2. Epub 2006 Apr 5.
Beta2-adrenergic receptor (beta2AR) gene polymorphisms have been reported to be associated with various asthma-related traits in different racial/ethnic populations. However, it is unknown whether beta2AR genetic variants are associated with asthma in African Americans. In this study, we have examined whether there is association between beta2AR genetic variants and asthma in African Americans. We have recruited 264 African American asthmatic subjects and 176 matched healthy controls participating in the Study of African Americans, Asthma, Genes and Environments (SAGE). We genotyped seven known and recently identified beta2AR SNP variants, then tested genotype and haplotype association of asthma-related traits with the beta2AR SNPs in our African American cohort with adjustment of confounding effect due to admixture background and environmental risk factors. We found a significant association of the SNP -47 (Arg-19Cys) polymorphism with DeltaFEF(25-75), a measure of bronchodilator drug responsiveness, in African American asthmatics after correction for multiple testing (P = 0.001). We did not observe association of the SNP +46 (Arg16Gly) variant with asthma disease diagnosis and asthma-related phenotypes. In contrast to previous results between the Arg16Gly variant and traits related to bronchodilator responsiveness, our results indicate that the Arg-19Cys polymorphism in beta upstream peptide may play an important role in bronchodilator drug responsiveness in African American subjects. Our findings highlight the importance of investigating genetic risk factors for asthma in different populations.
据报道,β2肾上腺素能受体(beta2AR)基因多态性与不同种族/族裔人群中各种哮喘相关特征有关。然而,尚不清楚beta2AR基因变异是否与非裔美国人的哮喘有关。在本研究中,我们调查了非裔美国人中beta2AR基因变异与哮喘之间是否存在关联。我们招募了264名非裔美国哮喘患者和176名匹配的健康对照,他们均参与了非裔美国人、哮喘、基因与环境研究(SAGE)。我们对7个已知的和最近鉴定出的beta2AR单核苷酸多态性(SNP)变异进行了基因分型,然后在我们的非裔美国队列中测试了哮喘相关特征与beta2AR SNPs的基因型和单倍型关联,并对由于混合背景和环境风险因素导致的混杂效应进行了校正。我们发现,在进行多重检验校正后,非裔美国哮喘患者中SNP -47(Arg-19Cys)多态性与DeltaFEF(25-75)(一种支气管扩张剂药物反应性指标)之间存在显著关联(P = 0.001)。我们未观察到SNP +46(Arg16Gly)变异与哮喘疾病诊断及哮喘相关表型之间存在关联。与先前关于Arg16Gly变异与支气管扩张剂反应性相关特征的研究结果相反,我们的结果表明,β上游肽中的Arg-19Cys多态性可能在非裔美国受试者的支气管扩张剂药物反应性中起重要作用。我们的研究结果突出了在不同人群中研究哮喘遗传风险因素的重要性。