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Effect of β(2) -adrenergic receptor gene Arg16Gly polymorphisms on response to long-acting β(2)-agonist in Chinese Han asthmatic patients
BACKGROUND: To evaluate the effect of variation of the Arg16Gly polymorphism of the β(2)-adrenergic receptor gene on clinical response to salmeterol administered with fluticasone propionate in Chinese Han asthmatic patients. METHODS: Moderate persistent asthmatic patients (n = 62) currently receivin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013543/ https://www.ncbi.nlm.nih.gov/pubmed/24721141 http://dx.doi.org/10.1186/2049-6958-9-22 |
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author | Qiu, Yuying Zhang, Deping Qin, Yu Yin, Kai-Sheng |
author_facet | Qiu, Yuying Zhang, Deping Qin, Yu Yin, Kai-Sheng |
author_sort | Qiu, Yuying |
collection | PubMed |
description | BACKGROUND: To evaluate the effect of variation of the Arg16Gly polymorphism of the β(2)-adrenergic receptor gene on clinical response to salmeterol administered with fluticasone propionate in Chinese Han asthmatic patients. METHODS: Moderate persistent asthmatic patients (n = 62) currently receiving short-acting β(2)-agonists were administered twice-daily therapy with salmeterol/fluticasone propionate 50/250 μg in a single inhaler for 12 weeks, followed by a 2-to-4-day run-out period. Using direct DNA sequencing, five single nucleotide polymorphisms (SNPs) in the promoter and coding block regions of β(2)-adrenergic receptor gene were determined in 62 subjects and haplotypes were combined. RESULTS: There was sustained and significant improvement (p < 0.001) over baseline in all measures of asthma control in subjects receiving salmeterol and fluticasone, regardless of Arg16Gly genotype. However, there was no significant difference in the improvement among three genotypes (p > 0.05). Responses to salmeterol did not appear to be modified by haplotype pairs (p > 0.05). During the run-out period, all subjects had similar decreases in measures of asthma control, with no differences between genotypes (p > 0.05). CONCLUSIONS: Response to salmeterol does not vary with Arg16Gly polymorphisms after chronic dosing with inhaled corticosteroids in Chinese Han asthmatic patients. |
format | Online Article Text |
id | pubmed-4013543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40135432014-05-09 Effect of β(2) -adrenergic receptor gene Arg16Gly polymorphisms on response to long-acting β(2)-agonist in Chinese Han asthmatic patients Qiu, Yuying Zhang, Deping Qin, Yu Yin, Kai-Sheng Multidiscip Respir Med Short Report BACKGROUND: To evaluate the effect of variation of the Arg16Gly polymorphism of the β(2)-adrenergic receptor gene on clinical response to salmeterol administered with fluticasone propionate in Chinese Han asthmatic patients. METHODS: Moderate persistent asthmatic patients (n = 62) currently receiving short-acting β(2)-agonists were administered twice-daily therapy with salmeterol/fluticasone propionate 50/250 μg in a single inhaler for 12 weeks, followed by a 2-to-4-day run-out period. Using direct DNA sequencing, five single nucleotide polymorphisms (SNPs) in the promoter and coding block regions of β(2)-adrenergic receptor gene were determined in 62 subjects and haplotypes were combined. RESULTS: There was sustained and significant improvement (p < 0.001) over baseline in all measures of asthma control in subjects receiving salmeterol and fluticasone, regardless of Arg16Gly genotype. However, there was no significant difference in the improvement among three genotypes (p > 0.05). Responses to salmeterol did not appear to be modified by haplotype pairs (p > 0.05). During the run-out period, all subjects had similar decreases in measures of asthma control, with no differences between genotypes (p > 0.05). CONCLUSIONS: Response to salmeterol does not vary with Arg16Gly polymorphisms after chronic dosing with inhaled corticosteroids in Chinese Han asthmatic patients. BioMed Central 2014-04-11 /pmc/articles/PMC4013543/ /pubmed/24721141 http://dx.doi.org/10.1186/2049-6958-9-22 Text en Copyright © 2014 Qiu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Qiu, Yuying Zhang, Deping Qin, Yu Yin, Kai-Sheng Effect of β(2) -adrenergic receptor gene Arg16Gly polymorphisms on response to long-acting β(2)-agonist in Chinese Han asthmatic patients |
title | Effect of β(2) -adrenergic receptor gene Arg16Gly polymorphisms on response to long-acting β(2)-agonist in Chinese Han asthmatic patients |
title_full | Effect of β(2) -adrenergic receptor gene Arg16Gly polymorphisms on response to long-acting β(2)-agonist in Chinese Han asthmatic patients |
title_fullStr | Effect of β(2) -adrenergic receptor gene Arg16Gly polymorphisms on response to long-acting β(2)-agonist in Chinese Han asthmatic patients |
title_full_unstemmed | Effect of β(2) -adrenergic receptor gene Arg16Gly polymorphisms on response to long-acting β(2)-agonist in Chinese Han asthmatic patients |
title_short | Effect of β(2) -adrenergic receptor gene Arg16Gly polymorphisms on response to long-acting β(2)-agonist in Chinese Han asthmatic patients |
title_sort | effect of β(2) -adrenergic receptor gene arg16gly polymorphisms on response to long-acting β(2)-agonist in chinese han asthmatic patients |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013543/ https://www.ncbi.nlm.nih.gov/pubmed/24721141 http://dx.doi.org/10.1186/2049-6958-9-22 |
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