Wu H, Romieu I, Sienra-Monge J-J, del Rio-Navarro B E, Burdett L, Yuenger J, Li H, Chanock S J, London S J
Laboratory of Respiratory Biology, Division of Intramural Research, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA.
Genes Immun. 2008 Apr;9(3):224-30. doi: 10.1038/gene.2008.8. Epub 2008 Mar 13.
G-protein-coupled receptor for asthma susceptibility (GPRA or GPR154) was identified as an asthma and atopy candidate gene by positional cloning. Some subsequent studies suggest associations of GPRA single nucleotide polymorphisms (SNPs) and haplotypes with asthma or atopy susceptibility. However, the associated SNPs or haplotypes vary among studies. The role of GPRA genetic variation in asthma and atopy remains unsolved. Published data on GRPA variants and asthma come exclusively from Caucasian and Asian populations. We examined whether GPRA SNPs and haplotypes are associated with asthma and atopy in a Mexican population. We genotyped and analyzed 27 GPRA SNPs in 589 nuclear families consisting of asthmatic children aged 4-17 years of age and their parents in Mexico City. Atopy was determined by skin prick tests to 25 aeroallergens. The 27 SNPs examined provided excellent coverage of the GPRA gene. GPRA SNPs and haplotypes were not associated with childhood asthma and the degree of atopy to aeroallergens in a Mexican population. Our review of studies of GPRA variants in relation to asthma phenotypes shows considerable heterogeneity. Accordingly, our results suggest that GPRA variants are not an important contributor to childhood asthma and atopy susceptibility in a Mexican population.
哮喘易感性G蛋白偶联受体(GPRA或GPR154)通过定位克隆被鉴定为哮喘和特应性候选基因。随后的一些研究表明,GPRA单核苷酸多态性(SNP)和单倍型与哮喘或特应性易感性有关。然而,相关的SNP或单倍型在不同研究中有所不同。GPRA基因变异在哮喘和特应性中的作用仍未解决。关于GRPA变异与哮喘的已发表数据仅来自白种人和亚洲人群。我们研究了GPRA SNP和单倍型在墨西哥人群中是否与哮喘和特应性相关。我们对墨西哥城589个核心家庭中的27个GPRA SNP进行了基因分型和分析,这些家庭由4至17岁的哮喘儿童及其父母组成。通过对25种空气过敏原进行皮肤点刺试验来确定特应性。所检测的27个SNP对GPRA基因具有良好的覆盖性。在墨西哥人群中,GPRA SNP和单倍型与儿童哮喘及对空气过敏原的特应性程度无关。我们对GPRA变异与哮喘表型相关研究的综述显示出相当大的异质性。因此,我们的结果表明,在墨西哥人群中,GPRA变异不是儿童哮喘和特应性易感性的重要因素。