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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...

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Autores principales: Reynolds, Wanda F., Sermet-Gaudelus, Isabelle, Gausson, Valérie, Feuillet, Marie-Noëlle, Bonnefont, Jean-Paul, Lenoir, Gérard, Descamps-Latscha, Béatrice, Witko-Sarsat, Véronique
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2006
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.
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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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