Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,

Detalhes bibliográficos
Autor(a) principal: Furlan,Larissa Lazzarini
Data de Publicação: 2017
Outros Autores: Ribeiro,José Dirceu, Bertuzzo,Carmen Sílvia, Salomão Junior,João Batista, Souza,Dorotéia Rossi Silva, Marson,Fernando Augusto Lima
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Jornal de Pediatria (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572017000600639
Resumo: Abstract Objective: Interleukin 8 protein promotes inflammatory responses, even in airways. The presence of interleukin 8 gene variants causes altered inflammatory responses and possibly varied responses to inhaled bronchodilators. Thus, this study analyzed the interleukin 8 variants (rs4073, rs2227306, and rs2227307) and their association with the response to inhaled bronchodilators in cystic fibrosis patients. Methods: Analysis of interleukin 8 gene variants was performed by restriction fragment length polymorphism of polymerase chain reaction. The association between spirometry markers and the response to inhaled bronchodilators was evaluated by Mann-Whitney and Kruskal-Wallis tests. The analysis included all cystic fibrosis patients, and subsequently patients with two mutations in the cystic fibrosis transmembrane conductance regulator gene belonging to classes I to III. Results: This study included 186 cystic fibrosis patients. There was no association of the rs2227307 variant with the response to inhaled bronchodilators. The rs2227306 variant was associated with FEF50% in the dominant group and in the group with two identified mutations in the cystic fibrosis transmembrane conductance regulator gene. The rs4073 variant was associated with spirometry markers in four genetic models: co-dominant (FEF25-75% and FEF75%), dominant (FEV1, FEF50%, FEF75%, and FEF25-75%), recessive (FEF75% and FEF25-75%), and over-dominant (FEV1/FVC). Conclusions: This study highlighted the importance of the rs4073 variant of the interleukin 8 gene, regarding response to inhaled bronchodilators, and of the assessment of mutations in the cystic fibrosis transmembrane conductance regulator gene.
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spelling Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,CFTRDisease severityInterleukin 8Lung functionAbstract Objective: Interleukin 8 protein promotes inflammatory responses, even in airways. The presence of interleukin 8 gene variants causes altered inflammatory responses and possibly varied responses to inhaled bronchodilators. Thus, this study analyzed the interleukin 8 variants (rs4073, rs2227306, and rs2227307) and their association with the response to inhaled bronchodilators in cystic fibrosis patients. Methods: Analysis of interleukin 8 gene variants was performed by restriction fragment length polymorphism of polymerase chain reaction. The association between spirometry markers and the response to inhaled bronchodilators was evaluated by Mann-Whitney and Kruskal-Wallis tests. The analysis included all cystic fibrosis patients, and subsequently patients with two mutations in the cystic fibrosis transmembrane conductance regulator gene belonging to classes I to III. Results: This study included 186 cystic fibrosis patients. There was no association of the rs2227307 variant with the response to inhaled bronchodilators. The rs2227306 variant was associated with FEF50% in the dominant group and in the group with two identified mutations in the cystic fibrosis transmembrane conductance regulator gene. The rs4073 variant was associated with spirometry markers in four genetic models: co-dominant (FEF25-75% and FEF75%), dominant (FEV1, FEF50%, FEF75%, and FEF25-75%), recessive (FEF75% and FEF25-75%), and over-dominant (FEV1/FVC). Conclusions: This study highlighted the importance of the rs4073 variant of the interleukin 8 gene, regarding response to inhaled bronchodilators, and of the assessment of mutations in the cystic fibrosis transmembrane conductance regulator gene.Sociedade Brasileira de Pediatria2017-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572017000600639Jornal de Pediatria v.93 n.6 2017reponame:Jornal de Pediatria (Online)instname:Sociedade Brasileira de Pediatria (SBP)instacron:SBPE10.1016/j.jped.2017.03.005info:eu-repo/semantics/openAccessFurlan,Larissa LazzariniRibeiro,José DirceuBertuzzo,Carmen SílviaSalomão Junior,João BatistaSouza,Dorotéia Rossi SilvaMarson,Fernando Augusto Limaeng2017-12-08T00:00:00Zoai:scielo:S0021-75572017000600639Revistahttp://www.jped.com.br/https://old.scielo.br/oai/scielo-oai.php||jped@jped.com.br1678-47820021-7557opendoar:2017-12-08T00:00Jornal de Pediatria (Online) - Sociedade Brasileira de Pediatria (SBP)false
dc.title.none.fl_str_mv Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,
title Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,
spellingShingle Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,
Furlan,Larissa Lazzarini
CFTR
Disease severity
Interleukin 8
Lung function
title_short Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,
title_full Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,
title_fullStr Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,
title_full_unstemmed Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,
title_sort Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis,
author Furlan,Larissa Lazzarini
author_facet Furlan,Larissa Lazzarini
Ribeiro,José Dirceu
Bertuzzo,Carmen Sílvia
Salomão Junior,João Batista
Souza,Dorotéia Rossi Silva
Marson,Fernando Augusto Lima
author_role author
author2 Ribeiro,José Dirceu
Bertuzzo,Carmen Sílvia
Salomão Junior,João Batista
Souza,Dorotéia Rossi Silva
Marson,Fernando Augusto Lima
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Furlan,Larissa Lazzarini
Ribeiro,José Dirceu
Bertuzzo,Carmen Sílvia
Salomão Junior,João Batista
Souza,Dorotéia Rossi Silva
Marson,Fernando Augusto Lima
dc.subject.por.fl_str_mv CFTR
Disease severity
Interleukin 8
Lung function
topic CFTR
Disease severity
Interleukin 8
Lung function
description Abstract Objective: Interleukin 8 protein promotes inflammatory responses, even in airways. The presence of interleukin 8 gene variants causes altered inflammatory responses and possibly varied responses to inhaled bronchodilators. Thus, this study analyzed the interleukin 8 variants (rs4073, rs2227306, and rs2227307) and their association with the response to inhaled bronchodilators in cystic fibrosis patients. Methods: Analysis of interleukin 8 gene variants was performed by restriction fragment length polymorphism of polymerase chain reaction. The association between spirometry markers and the response to inhaled bronchodilators was evaluated by Mann-Whitney and Kruskal-Wallis tests. The analysis included all cystic fibrosis patients, and subsequently patients with two mutations in the cystic fibrosis transmembrane conductance regulator gene belonging to classes I to III. Results: This study included 186 cystic fibrosis patients. There was no association of the rs2227307 variant with the response to inhaled bronchodilators. The rs2227306 variant was associated with FEF50% in the dominant group and in the group with two identified mutations in the cystic fibrosis transmembrane conductance regulator gene. The rs4073 variant was associated with spirometry markers in four genetic models: co-dominant (FEF25-75% and FEF75%), dominant (FEV1, FEF50%, FEF75%, and FEF25-75%), recessive (FEF75% and FEF25-75%), and over-dominant (FEV1/FVC). Conclusions: This study highlighted the importance of the rs4073 variant of the interleukin 8 gene, regarding response to inhaled bronchodilators, and of the assessment of mutations in the cystic fibrosis transmembrane conductance regulator gene.
publishDate 2017
dc.date.none.fl_str_mv 2017-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572017000600639
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.jped.2017.03.005
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Pediatria
publisher.none.fl_str_mv Sociedade Brasileira de Pediatria
dc.source.none.fl_str_mv Jornal de Pediatria v.93 n.6 2017
reponame:Jornal de Pediatria (Online)
instname:Sociedade Brasileira de Pediatria (SBP)
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reponame_str Jornal de Pediatria (Online)
collection Jornal de Pediatria (Online)
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repository.mail.fl_str_mv ||jped@jped.com.br
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