β2-Adrenergic Receptor Haplotype may be Associated with Susceptibility to Desensitization to Long-Acting β2-Agonists in COPD Patients
Purpose Τhat β2-adrenergic receptor (β2AR) haplotypes may play a key role in clinical response to β2-agonists and haplotype Cys-19Gly16Gln27 ( CysGlyGln ) is reported to be associated with desensitization of β2AR to β-agonists in lymphocytes isolated from patients with asthma and septic shock. We so...
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Veröffentlicht in: | Lung 2012-08, Vol.190 (4), p.411-417 |
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Sprache: | eng |
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Zusammenfassung: | Purpose
Τhat β2-adrenergic receptor (β2AR) haplotypes may play a key role in clinical response to β2-agonists and haplotype
Cys-19Gly16Gln27
(
CysGlyGln
) is reported to be associated with desensitization of β2AR to β-agonists in lymphocytes isolated from patients with asthma and septic shock. We sought to determine whether haplotypic variation of the β2AR affects the functional outcomes of long-acting β2-agonist (LABA) treatment for chronic obstructive pulmonary disease (COPD) when used as monotherapy.
Methods
Treatment-naïve patients with COPD (
n
= 36) were prospectively treated with two kinds of LABA—inhaled salmeterol and transdermal tulobuterol patch—for 12 weeks in crossover study, and changes in pulmonary function data and 6-minute walk distance (6MWD) were compared between groups stratified by the
CysGlyGln
.
Results
Frequencies of haplotype and diplotype for the
CysGlyGln
were 0.51 and 0.36, respectively. The individuals homozygous for
CysGlyGln
showed less improvement in FEV
1
, %FEF
25−75 %
, and IC/TLC than those with 0 or 1 copy of
CysGlyGln
after treatment with both LABAs despite initial bronchodilator responses to albuterol being similar in these groups. The response in these parameters was not significantly different between two types of LABA. Overall changes in 6MWD in individuals with 2 copies of
CysGlyGln
versus 0 or 1 copy for salmeterol were 2.8 and 11 m, and for tulobuterol were −1.3 and 16 m, respectively.
Conclusions
Homozygous haplotype for the
CysGlyGln
of β2AR may be associated with susceptibility to desensitization to LABA in patients with COPD. |
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ISSN: | 0341-2040 1432-1750 |
DOI: | 10.1007/s00408-012-9387-7 |