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MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort

Background and objective: Dysregulation of respiratory mucins, MUC5AC in particular, has been implicated in respiratory disease and MUC5AC expression is up-regulated in response to environmental challenges and inflammatory mediators. The aim of this study was to examine the effect of genetic variati...

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Autores principales: Johnson, Lauren, Shah, Imran, Loh, Andrew X, Vinall, Lynne E, Teixeira, Ana S, Rousseau, Karine, Holloway, John W, Hardy, Rebecca, Swallow, Dallas M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784974/
https://www.ncbi.nlm.nih.gov/pubmed/23551418
http://dx.doi.org/10.1111/resp.12092
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author Johnson, Lauren
Shah, Imran
Loh, Andrew X
Vinall, Lynne E
Teixeira, Ana S
Rousseau, Karine
Holloway, John W
Hardy, Rebecca
Swallow, Dallas M
author_facet Johnson, Lauren
Shah, Imran
Loh, Andrew X
Vinall, Lynne E
Teixeira, Ana S
Rousseau, Karine
Holloway, John W
Hardy, Rebecca
Swallow, Dallas M
author_sort Johnson, Lauren
collection PubMed
description Background and objective: Dysregulation of respiratory mucins, MUC5AC in particular, has been implicated in respiratory disease and MUC5AC expression is up-regulated in response to environmental challenges and inflammatory mediators. The aim of this study was to examine the effect of genetic variation on susceptibility to common respiratory conditions. Methods: The association of MUC5AC and the closely linked genes MUC2 and MUC5B with respiratory outcomes was tested in the MRC National Survey of Health and Development, a longitudinal birth cohort of men and women born in 1946. Also examined were the functional variants of the genes encoding inflammatory mediators, IL13, IL1B, IL1RN, TNFA and ERBB1, for which there is a likely influence on MUC5AC expression and were explored potential gene-gene interactions with these inflammatory mediators. Results: Statistically significant associations between the 3'ter MUC5AC simple nucleotide polymorphism (SNP) rs1132440 and various non-independent respiratory outcomes (bronchitis, wheeze, asthma, hay fever) were reported while the adjacent loci show slight (but largely non-statistically significant) differences, presumably reflective of linkage disequilibrium (allelic association) across the region. A novel association between bronchitis and a non-synonymous functional ERBB1 SNP, rs2227983 (aka epidermal growth factor receptor:R497K, R521K) is also reported and evidence presented of interaction between MUC5AC and ERBB1 and between MUC5AC and IL1RN with respect to bronchitis. The ERBB1 result suggests a clear mechanism for a biological interaction in which the allelic variants of epidermal growth factor receptor differentially affect mucin expression. Conclusions: The MUC5AC association and the interactions with inflammatory mediators suggest that genetically determined differences in MUC5AC expression alter susceptibility to respiratory disease. SUMMARY AT A GLANCE This longitudinal cohort study shows occurrence of the common respiratory conditions bronchitis, wheeze, asthma and hay fever to be associated with genetic variation in a mucin gene, MUC5AC. Functional variation in the epidermal growth factor receptor (epidermal growth factor receptor encoded by ERBB1) is also associated with bronchitis and modulates the MUC5AC effect.
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spelling pubmed-37849742013-10-01 MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort Johnson, Lauren Shah, Imran Loh, Andrew X Vinall, Lynne E Teixeira, Ana S Rousseau, Karine Holloway, John W Hardy, Rebecca Swallow, Dallas M Respirology Original Articles Background and objective: Dysregulation of respiratory mucins, MUC5AC in particular, has been implicated in respiratory disease and MUC5AC expression is up-regulated in response to environmental challenges and inflammatory mediators. The aim of this study was to examine the effect of genetic variation on susceptibility to common respiratory conditions. Methods: The association of MUC5AC and the closely linked genes MUC2 and MUC5B with respiratory outcomes was tested in the MRC National Survey of Health and Development, a longitudinal birth cohort of men and women born in 1946. Also examined were the functional variants of the genes encoding inflammatory mediators, IL13, IL1B, IL1RN, TNFA and ERBB1, for which there is a likely influence on MUC5AC expression and were explored potential gene-gene interactions with these inflammatory mediators. Results: Statistically significant associations between the 3'ter MUC5AC simple nucleotide polymorphism (SNP) rs1132440 and various non-independent respiratory outcomes (bronchitis, wheeze, asthma, hay fever) were reported while the adjacent loci show slight (but largely non-statistically significant) differences, presumably reflective of linkage disequilibrium (allelic association) across the region. A novel association between bronchitis and a non-synonymous functional ERBB1 SNP, rs2227983 (aka epidermal growth factor receptor:R497K, R521K) is also reported and evidence presented of interaction between MUC5AC and ERBB1 and between MUC5AC and IL1RN with respect to bronchitis. The ERBB1 result suggests a clear mechanism for a biological interaction in which the allelic variants of epidermal growth factor receptor differentially affect mucin expression. Conclusions: The MUC5AC association and the interactions with inflammatory mediators suggest that genetically determined differences in MUC5AC expression alter susceptibility to respiratory disease. SUMMARY AT A GLANCE This longitudinal cohort study shows occurrence of the common respiratory conditions bronchitis, wheeze, asthma and hay fever to be associated with genetic variation in a mucin gene, MUC5AC. Functional variation in the epidermal growth factor receptor (epidermal growth factor receptor encoded by ERBB1) is also associated with bronchitis and modulates the MUC5AC effect. Blackwell Publishing Ltd 2013-08 2013-07-25 /pmc/articles/PMC3784974/ /pubmed/23551418 http://dx.doi.org/10.1111/resp.12092 Text en Respirology © 2013 Asian Pacific Society of Respirology http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Johnson, Lauren
Shah, Imran
Loh, Andrew X
Vinall, Lynne E
Teixeira, Ana S
Rousseau, Karine
Holloway, John W
Hardy, Rebecca
Swallow, Dallas M
MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort
title MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort
title_full MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort
title_fullStr MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort
title_full_unstemmed MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort
title_short MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort
title_sort muc5ac and inflammatory mediators associated with respiratory outcomes in the british 1946 birth cohort
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784974/
https://www.ncbi.nlm.nih.gov/pubmed/23551418
http://dx.doi.org/10.1111/resp.12092
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