Arvind Manoharan1, William J Anderson, Brian J Lipworth. 1. Asthma and Allergy Research Group, Division of Cardiovascular and Diabetes Medicine, Medical Research Institute, University of Dundee, Dundee, Scotland.
Abstract
BACKGROUND: We previously reported that the β(2)-adrenergic receptor (ADRB2) polymorphism had no effect on bronchial hyperresponsiveness (BHR) to methacholine in asthmatic patients. We have now replicated this analysis in a different and larger cohort of patients. OBJECTIVE: To assess the effect of the ADRB2 polymorphism in methacholine-responsive patients with asthma. METHODS: We conducted a retrospective analysis of the effects of ADRB2 haplotypes at position 16 (Gly/Arg) and 27(Gln/Glu) in 449 patients with a physician diagnosis of asthma who were responsive to methacholine (ie, provocation concentration that caused a decrease in forced expiratory volume in 1 second [FEV(1)] of 20% [PC(20)], <8 mg/mL). RESULTS: No differences were found in age, FEV(1), or inhaled corticosteroid dose among the genotypes or haplotypes. No significant differences were found in methacholine PC(20) (ie, <8 mg/mL) between the separate genotypes at position 16 or 27 or between the haplotypes at positions 16/27 combined. In addition, no significant differences were found among individual genotypes when stratified according to severity of BHR using different doubling dilution cutoff points for methacholine PC(20) (ie, <4 mg/mL, <2 mg/mL, and <1 mg/mL). CONCLUSION: We have confirmed in this replication study that common ADRB2 genotypes or haplotypes at positions 16/27 do not influence BHR in methacholine-responsive patients with asthma.
BACKGROUND: We previously reported that the β(2)-adrenergic receptor (ADRB2) polymorphism had no effect on bronchial hyperresponsiveness (BHR) to methacholine in asthmatic patients. We have now replicated this analysis in a different and larger cohort of patients. OBJECTIVE: To assess the effect of the ADRB2 polymorphism in methacholine-responsive patients with asthma. METHODS: We conducted a retrospective analysis of the effects of ADRB2 haplotypes at position 16 (Gly/Arg) and 27(Gln/Glu) in 449 patients with a physician diagnosis of asthma who were responsive to methacholine (ie, provocation concentration that caused a decrease in forced expiratory volume in 1 second [FEV(1)] of 20% [PC(20)], <8 mg/mL). RESULTS: No differences were found in age, FEV(1), or inhaled corticosteroid dose among the genotypes or haplotypes. No significant differences were found in methacholine PC(20) (ie, <8 mg/mL) between the separate genotypes at position 16 or 27 or between the haplotypes at positions 16/27 combined. In addition, no significant differences were found among individual genotypes when stratified according to severity of BHR using different doubling dilution cutoff points for methacholine PC(20) (ie, <4 mg/mL, <2 mg/mL, and <1 mg/mL). CONCLUSION: We have confirmed in this replication study that common ADRB2 genotypes or haplotypes at positions 16/27 do not influence BHR in methacholine-responsive patients with asthma.
Authors: Ana Carolina Zimiani de Paiva; Fernando Augusto de Lima Marson; José Dirceu Ribeiro; Carmen Sílvia Bertuzzo Journal: Allergy Asthma Clin Immunol Date: 2014-02-05 Impact factor: 3.406
Authors: Li Ping Chung; Svetlana Baltic; Manuel Ferreira; Suzanna Temple; Grant Waterer; Philip J Thompson Journal: PLoS One Date: 2014-04-01 Impact factor: 3.240
Authors: Sunny Jabbal; Arvind Manoharan; Joseph Lipworth; William Anderson; Philip Short; Brian Lipworth Journal: Lung Date: 2016-02-15 Impact factor: 2.584