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Myeloperoxidase Promoter Polymorphism −463G Is Associated With More Severe Clinical Expression of Cystic Fibrosis Pulmonary Disease
The severity of cystic fibrosis (CF) pulmonary disease is not directly related to CFTR genotype but depends upon several parameters, including neutrophil-dominated inflammation. Identification of agents modulating inflammation constitutes a relevant goal. Myeloperoxidase (MPO) is involved in both mi...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592586/ https://www.ncbi.nlm.nih.gov/pubmed/16883063 http://dx.doi.org/10.1155/MI/2006/36735 |
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author | Reynolds, Wanda F. Sermet-Gaudelus, Isabelle Gausson, Valérie Feuillet, Marie-Noëlle Bonnefont, Jean-Paul Lenoir, Gérard Descamps-Latscha, Béatrice Witko-Sarsat, Véronique |
author_facet | Reynolds, Wanda F. Sermet-Gaudelus, Isabelle Gausson, Valérie Feuillet, Marie-Noëlle Bonnefont, Jean-Paul Lenoir, Gérard Descamps-Latscha, Béatrice Witko-Sarsat, Véronique |
author_sort | Reynolds, Wanda F. |
collection | PubMed |
description | The severity of cystic fibrosis (CF) pulmonary disease is not directly related to CFTR genotype but depends upon several parameters, including neutrophil-dominated inflammation. Identification of agents modulating inflammation constitutes a relevant goal. Myeloperoxidase (MPO) is involved in both microbicidal and proinflammatory neutrophil activities. The aim of this study was to evaluate whether the −463GA MPO promoter polymorphism is linked to clinical severity of CF-associated pulmonary inflammation. This polymorphism significantly affects the level of MPO gene expression in leukocytes and the G allele is more expressing than the A allele. We show that MPO genotype significantly influences the severity of pulmonary disease in early stages, prior to the development of chronic lung infections, with GG genotype being associated with more severe CF disease. Our findings indicate that the level of MPO gene expression influences the CF pathogenesis, presumably reflecting cellular damage by MPO-generated oxidants or other activity of MPO in airway inflammation. |
format | Text |
id | pubmed-1592586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-15925862006-10-23 Myeloperoxidase Promoter Polymorphism −463G Is Associated With More Severe Clinical Expression of Cystic Fibrosis Pulmonary Disease Reynolds, Wanda F. Sermet-Gaudelus, Isabelle Gausson, Valérie Feuillet, Marie-Noëlle Bonnefont, Jean-Paul Lenoir, Gérard Descamps-Latscha, Béatrice Witko-Sarsat, Véronique Mediators Inflamm Research Communication The severity of cystic fibrosis (CF) pulmonary disease is not directly related to CFTR genotype but depends upon several parameters, including neutrophil-dominated inflammation. Identification of agents modulating inflammation constitutes a relevant goal. Myeloperoxidase (MPO) is involved in both microbicidal and proinflammatory neutrophil activities. The aim of this study was to evaluate whether the −463GA MPO promoter polymorphism is linked to clinical severity of CF-associated pulmonary inflammation. This polymorphism significantly affects the level of MPO gene expression in leukocytes and the G allele is more expressing than the A allele. We show that MPO genotype significantly influences the severity of pulmonary disease in early stages, prior to the development of chronic lung infections, with GG genotype being associated with more severe CF disease. Our findings indicate that the level of MPO gene expression influences the CF pathogenesis, presumably reflecting cellular damage by MPO-generated oxidants or other activity of MPO in airway inflammation. Hindawi Publishing Corporation 2006 2006-03-14 /pmc/articles/PMC1592586/ /pubmed/16883063 http://dx.doi.org/10.1155/MI/2006/36735 Text en Copyright © 2006 Wanda F. Reynolds et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Communication Reynolds, Wanda F. Sermet-Gaudelus, Isabelle Gausson, Valérie Feuillet, Marie-Noëlle Bonnefont, Jean-Paul Lenoir, Gérard Descamps-Latscha, Béatrice Witko-Sarsat, Véronique Myeloperoxidase Promoter Polymorphism −463G Is Associated With More Severe Clinical Expression of Cystic Fibrosis Pulmonary Disease |
title | Myeloperoxidase Promoter Polymorphism −463G
Is Associated With More Severe Clinical Expression of Cystic
Fibrosis Pulmonary Disease |
title_full | Myeloperoxidase Promoter Polymorphism −463G
Is Associated With More Severe Clinical Expression of Cystic
Fibrosis Pulmonary Disease |
title_fullStr | Myeloperoxidase Promoter Polymorphism −463G
Is Associated With More Severe Clinical Expression of Cystic
Fibrosis Pulmonary Disease |
title_full_unstemmed | Myeloperoxidase Promoter Polymorphism −463G
Is Associated With More Severe Clinical Expression of Cystic
Fibrosis Pulmonary Disease |
title_short | Myeloperoxidase Promoter Polymorphism −463G
Is Associated With More Severe Clinical Expression of Cystic
Fibrosis Pulmonary Disease |
title_sort | myeloperoxidase promoter polymorphism −463g
is associated with more severe clinical expression of cystic
fibrosis pulmonary disease |
topic | Research Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592586/ https://www.ncbi.nlm.nih.gov/pubmed/16883063 http://dx.doi.org/10.1155/MI/2006/36735 |
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