β2-Adrenergic receptor polymorphisms: pharmacogenetic response to bronchodilator among African American asthmatics

被引:0
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作者
Hui-Ju Tsai
Nishat Shaikh
Jennifer Y. Kho
Natalie Battle
Mariam Naqvi
Daniel Navarro
Henry Matallana
Craig M. Lilly
Celeste S. Eng
Gunjan Kumar
Shannon Thyne
H. George Watson
Kelley Meade
Michael LeNoir
Shweta Choudhry
Esteban G. Burchard
机构
[1] University of California,Department of Medicine
[2] University of California,Center for Human Genetics
[3] San Francisco General Hospital,Lung Biology Center
[4] Brigham and Women’s Hospital,undefined
[5] The James A. Watson Wellness Center,undefined
[6] Children’s Hospital and Research Institute,undefined
[7] Bay Area Pediatrics,undefined
来源
Human Genetics | 2006年 / 119卷
关键词
Asthma; Asthma Severity; Albuterol; Asthmatic Case; African American Subject;
D O I
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学科分类号
摘要
β2-Adrenergic receptor (β2AR) gene polymorphisms have been reported to be associated with various asthma-related traits in different racial/ethnic populations. However, it is unknown whether β2AR genetic variants are associated with asthma in African Americans. In this study, we have examined whether there is association between β2AR 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 β2AR SNP variants, then tested genotype and haplotype association of asthma-related traits with the β2AR 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 ΔFEF25–75, 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 β 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.
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