Association between β‐adrenoceptor gene polymorphisms and relative response to β₂‐agonists and anticholinergic drugs in Japanese asthmatic patients

<jats:title>ABSTRACT</jats:title><jats:p><jats:bold>Background and objective: </jats:bold> Whether β<jats:sub>2</jats:sub>‐adrenoceptor gene (<jats:italic>ADRB2</jats:italic>) polymorphisms are associated with airway responsiveness to β<jats:sub>2</jats:sub>‐agonist medications remains controversial, partly due to factors that may confound pharmacogenetic associations, including age, cigarette smoking and airway remodelling. To overcome these problems, we performed an analysis using parameters that reflected the specific bronchodilator response to β<jats:sub>2</jats:sub>‐agonists.</jats:p><jats:p><jats:bold>Methods: </jats:bold> The increases in FEV<jats:sub>1</jats:sub> after inhalation of procaterol hydrochloride (ΔFEV<jats:sub>1</jats:sub> procaterol) or oxitropium bromide (ΔFEV<jats:sub>1</jats:sub> oxitropium), and after sequential inhalation of procaterol and oxitropium (total airway reversibility), were measured in 81 Japanese patients with moderate to severe asthma. Approximately 3 kb of the DNA sequence of the coding and 5′‐flanking regions of <jats:italic>ADRB2</jats:italic> were genotyped by direct sequencing and PCR‐restriction fragment length polymorphism assay.</jats:p><jats:p><jats:bold>Results: </jats:bold> The mean age of the participants was 54 years, and 38 (47%) were smokers. Although ΔFEV<jats:sub>1</jats:sub> procaterol and ΔFEV<jats:sub>1</jats:sub> oxitropium adjusted for predicted FEV<jats:sub>1</jats:sub> were not associated with <jats:italic>ADRB2</jats:italic> polymorphisms, the ratio of ΔFEV<jats:sub>1</jats:sub> procaterol to total airway reversibility was significantly associated with the <jats:italic>ADRB2</jats:italic> A46G genotype (<jats:italic>P</jats:italic> < 0.05). Patients who were homozygous for the A46 allele (arginine at amino acid 16) were more responsive than carriers of the G46 (glycine 16) allele (<jats:italic>P</jats:italic> = 0.008). Multivariate linear regression analysis showed that ΔFEV<jats:sub>1</jats:sub> procaterol was correlated with the number of A46 alleles (<jats:italic>P</jats:italic> = 0.014), and also with total airway reversibility (<jats:italic>P</jats:italic> < 0.001) and smoking index in current smokers (<jats:italic>P</jats:italic> = 0.009).</jats:p><jats:p><jats:bold>Conclusions: </jats:bold> The <jats:italic>ADRB2</jats:italic> A46G polymorphism was associated with a relatively greater bronchodilator responsiveness to β<jats:sub>2</jats:sub>‐agonists even in elderly asthmatic patients and smokers.</jats:p>