Summary
What is known and objective:â Inhaled combination therapy composing of longâacting ÎČ2âagonist and corticosteroid has been widely applied in the management of asthma, but observed treatment responses vary. The aim of this study was to evaluate the pharmacogenetic effect of the adenylyl cyclase type 9 (ADCY9) gene polymorphism on combination therapy.
Materials and methods:â Eightyâsix mild to moderate Korean asthmatics were enrolled in this clinical trial. After the 2âweek ârunâinâ period, patients received budesonide (an inhaled corticosteroid) and formoterol (longâacting ÎČ2âagonist) during the following 12âweek active treatment period. Forced expiratory volume in 1âs (FEV1) and maximum midâexpiratory flow (MMEF) levels were measured at all visits as primary outcome. ADCY9 (Ile772Met, 150127 C/T, 150130 C/T, 150397 C/T, 150479 C/T, TTTA 5/4) and ÎČ2âadrenergic receptor (ADRB2, Arg16Gly) gene polymorphisms were genotyped.
Results:â Significant associations were observed between the ADCY9 single nucleotide polymorphisms and percent changes in FEV1 (Ile772Met T/C, Pâ=â0·030) and MMEF (150397 C/T, Pâ=â0·016) after 8âweeks of combination therapy. Haplotype associations were also observed with respect to percent changes in FEV1 after 8âweeks of therapy (Ht3[TTCC], Pâ=â0·017). Additive therapeutic effect was observed in those with the ADCY9 Ile772Met and ADRB2 Arg16Gly gene polymorphisms in terms of percent change in FEV1 after 8 and 12âweeks of therapy (Pâ=â0·002 and Pâ=â0·027 respectively).
What is new and conclusion:â Our results suggest that ADCY9 gene polymorphisms may alone, and in combination with ADRB2 gene polymorphisms, contribute to individual response to combination therapy in mild to moderate asthmatics.