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Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease

BACKGROUND: Chronic bronchitis (CB) is one of the classic phenotypes of COPD. The aims of our study were to investigate genetic variants associated with COPD subjects with CB relative to smokers with normal spirometry, and to assess for genetic differences between subjects with CB and without CB wit...

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Autores principales: Lee, Jin Hwa, Cho, Michael H, Hersh, Craig P, McDonald, Merry-Lynn N, Crapo, James D, Bakke, Per S, Gulsvik, Amund, Comellas, Alejandro P, Wendt, Christine H, Lomas, David A, Kim, Victor, Silverman, Edwin K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190389/
https://www.ncbi.nlm.nih.gov/pubmed/25241909
http://dx.doi.org/10.1186/s12931-014-0113-2
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author Lee, Jin Hwa
Cho, Michael H
Hersh, Craig P
McDonald, Merry-Lynn N
Crapo, James D
Bakke, Per S
Gulsvik, Amund
Comellas, Alejandro P
Wendt, Christine H
Lomas, David A
Kim, Victor
Silverman, Edwin K
author_facet Lee, Jin Hwa
Cho, Michael H
Hersh, Craig P
McDonald, Merry-Lynn N
Crapo, James D
Bakke, Per S
Gulsvik, Amund
Comellas, Alejandro P
Wendt, Christine H
Lomas, David A
Kim, Victor
Silverman, Edwin K
author_sort Lee, Jin Hwa
collection PubMed
description BACKGROUND: Chronic bronchitis (CB) is one of the classic phenotypes of COPD. The aims of our study were to investigate genetic variants associated with COPD subjects with CB relative to smokers with normal spirometry, and to assess for genetic differences between subjects with CB and without CB within the COPD population. METHODS: We analyzed data from current and former smokers from three cohorts: the COPDGene Study; GenKOLS (Bergen, Norway); and the Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE). CB was defined as having a cough productive of phlegm on most days for at least 3 consecutive months per year for at least 2 consecutive years. CB COPD cases were defined as having both CB and at least moderate COPD based on spirometry. Our primary analysis used smokers with normal spirometry as controls; secondary analysis was performed using COPD subjects without CB as controls. Genotyping was performed on Illumina platforms; results were summarized using fixed-effect meta-analysis. RESULTS: For CB COPD relative to smoking controls, we identified a new genome-wide significant locus on chromosome 11p15.5 (rs34391416, OR = 1.93, P = 4.99 × 10(-8)) as well as significant associations of known COPD SNPs within FAM13A. In addition, a GWAS of CB relative to those without CB within COPD subjects showed suggestive evidence for association on 1q23.3 (rs114931935, OR = 1.88, P = 4.99 × 10(-7)). CONCLUSIONS: We found genome-wide significant associations with CB COPD on 4q22.1 (FAM13A) and 11p15.5 (EFCAB4A, CHID1 and AP2A2), and a locus associated with CB within COPD subjects on 1q23.3 (RPL31P11 and ATF6). This study provides further evidence that genetic variants may contribute to phenotypic heterogeneity of COPD. TRIAL REGISTRATION: ClinicalTrials.gov NCT00608764, NCT00292552 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-014-0113-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-41903892014-10-10 Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease Lee, Jin Hwa Cho, Michael H Hersh, Craig P McDonald, Merry-Lynn N Crapo, James D Bakke, Per S Gulsvik, Amund Comellas, Alejandro P Wendt, Christine H Lomas, David A Kim, Victor Silverman, Edwin K Respir Res Research BACKGROUND: Chronic bronchitis (CB) is one of the classic phenotypes of COPD. The aims of our study were to investigate genetic variants associated with COPD subjects with CB relative to smokers with normal spirometry, and to assess for genetic differences between subjects with CB and without CB within the COPD population. METHODS: We analyzed data from current and former smokers from three cohorts: the COPDGene Study; GenKOLS (Bergen, Norway); and the Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE). CB was defined as having a cough productive of phlegm on most days for at least 3 consecutive months per year for at least 2 consecutive years. CB COPD cases were defined as having both CB and at least moderate COPD based on spirometry. Our primary analysis used smokers with normal spirometry as controls; secondary analysis was performed using COPD subjects without CB as controls. Genotyping was performed on Illumina platforms; results were summarized using fixed-effect meta-analysis. RESULTS: For CB COPD relative to smoking controls, we identified a new genome-wide significant locus on chromosome 11p15.5 (rs34391416, OR = 1.93, P = 4.99 × 10(-8)) as well as significant associations of known COPD SNPs within FAM13A. In addition, a GWAS of CB relative to those without CB within COPD subjects showed suggestive evidence for association on 1q23.3 (rs114931935, OR = 1.88, P = 4.99 × 10(-7)). CONCLUSIONS: We found genome-wide significant associations with CB COPD on 4q22.1 (FAM13A) and 11p15.5 (EFCAB4A, CHID1 and AP2A2), and a locus associated with CB within COPD subjects on 1q23.3 (RPL31P11 and ATF6). This study provides further evidence that genetic variants may contribute to phenotypic heterogeneity of COPD. TRIAL REGISTRATION: ClinicalTrials.gov NCT00608764, NCT00292552 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-014-0113-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-21 2014 /pmc/articles/PMC4190389/ /pubmed/25241909 http://dx.doi.org/10.1186/s12931-014-0113-2 Text en © Lee et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), 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 Research
Lee, Jin Hwa
Cho, Michael H
Hersh, Craig P
McDonald, Merry-Lynn N
Crapo, James D
Bakke, Per S
Gulsvik, Amund
Comellas, Alejandro P
Wendt, Christine H
Lomas, David A
Kim, Victor
Silverman, Edwin K
Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease
title Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease
title_full Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease
title_fullStr Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease
title_full_unstemmed Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease
title_short Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease
title_sort genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190389/
https://www.ncbi.nlm.nih.gov/pubmed/25241909
http://dx.doi.org/10.1186/s12931-014-0113-2
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