Association between genetic polymorphisms of the β2-adrenoceptor and response to albuterol in children with and without a history of wheezing

Fernando D. Martinez, Penelope E. Graves, Mauro Baldini, Susan Solomon, Robert Erickson

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578 Scopus citations


The β2-adrenergic receptor (β2AR) agonists are the most widely used agents in the treatment of asthma, but the genetic determinants of responsiveness to these agents are unknown. Two polymorphic loci within the coding region of the β2AR have been recently described at amino acids 16 and 27. It has been reported that glycine at codon 16 (Gly-16) is associated with increased agonist-promoted downregulation of the β2AR as compared with arginine-16 (Arg-16). The form of the receptor with glutamic acid at codon 27 (Glu-27), on the other hand, has been shown to be resistant to downregulation when compared with glutamine-27 (Gln-27), but only when coexpressed with Arg- 16. To assess if different genotypes of these two polymorphisms would show differential responses to inhaled β2AR agonists, we genotyped 269 children who were participants in a longitudinal study of asthma. Spirometry was performed before and after administration of 180 μg of albuterol, and a positive response was considered an increase of >15.3% predicted FEV1. There was marked linkage disequilibrium between the two polymorphisms, with 97.8% of all chromosomes that carried Arg-16 also carrying Gln-27. When compared to homozygotes for Gly-16, homozygotes for Arg-16 were 5.3 times (95% confidence interval 1.6-17.7) and heterozygores for β2AR-16 were 2.3 times (1.3-4.2) more likely to respond to albuterol, respectively. Similar trends were observed for asthmatic and nonasthmatic children, and results were independent of baseline lung function, ethnic origin, and previous use of antiasthma medication. No association was found between the β2AR-27 polymorphism and response to albuterol. These results may explain some of the variability in response to therapeutic doses of albuterol in children.

Original languageEnglish (US)
Pages (from-to)3184-3188
Number of pages5
JournalJournal of Clinical Investigation
Issue number12
StatePublished - Dec 15 1997


  • Asthma
  • Genetics
  • β-adrenergic receptor
  • β-agonists

ASJC Scopus subject areas

  • General Medicine


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