4.3 Article Proceedings Paper

Effect of polymorphism of the beta(2)-adrenergic receptor on response to regular use of albuterol in asthma

Journal

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
Volume 124, Issue 1-3, Pages 183-186

Publisher

KARGER
DOI: 10.1159/000053705

Keywords

asthma; beta(2)-adrenergic agonists; beta(2)-adrenergic receptor; albuterol

Funding

  1. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [U10HL051831, P01HL041496, U10HL051823, U10HL051810, R01HL045967, U10HL051845, U10HL051843, U10HL051834] Funding Source: NIH RePORTER
  2. NHLBI NIH HHS [U10 HL 51843, U10 HL 51834, U10 HL 51831, R01 HL 45967, U10 HL 51810, P01 HL 41496, U10 HL 51845, U10 HL 51823] Funding Source: Medline

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Background: Regular use of inhaled beta -adrenergic agonists may have adverse effects in some asthma patients. Polymorphisms of the beta (2)-adrenergic receptor (beta (2)-AR) can affect its regulation; however, results of smaller studies of the effects of such polymorphisms on response to beta -agonist therapy have been inconsistent. Methods: We examined the possible effects of polymorphisms at codons 16 (beta (2)-AR-16) and 27 (beta (2)-AR-27) on response to albuterol by genotyping 190 asthmatics who had participated in a trial of regular versus as-needed albuterol use. Results: During the 16-week treatment period, patients homozygous for arginine (Arg/Arg) at beta (2)-AR-16 who used albuterol regularly had a small decline in morning peak expiratory flow (AM PEF). Th is effect was magnified during a 4-week run-out period, when all patients returned to as-needed albuterol only. By the end of the study, Arg/Arg subjects who had used albuterol regularly had an AM PEF 30.5 +/- 12.1 liters/min lower (p = 0.012) than Arg/Arg patients who had used albuterol as needed only. Subjects homozygous for glycine at beta (2)-AR-16 showed no such decline. Evening PEF also declined in the Arg/Arg regular but not in as-need albuterol users. No significant differences between regular and asneeded treatment were associated with polymorphisms at beta (2)-AR-27. Conclusions: Polymorphisms of the beta (2)-AR may influence airway responses to regular inhaled beta -agonist treatment. Copyright (C) 2001 S. Karger AG, Basel.

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