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Lung microbiota associations with clinical features of COPD in the SPIROMICS cohort

Chronic obstructive pulmonary disease (COPD) is heterogeneous in development, progression, and phenotypes. Little is known about the lung microbiome, sampled by bronchoscopy, in milder COPD and its relationships to clinical features that reflect disease heterogeneity (lung function, symptom burden,...

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Autores principales: Opron, Kristopher, Begley, Lesa A., Erb-Downward, John R., Freeman, Christine, Madapoosi, Siddharth, Alexis, Neil E., Barjaktarevic, Igor, Graham Barr, R., Bleecker, Eugene R., Bowler, Russell P., Christenson, Stephanie A., Comellas, Alejandro P., Cooper, Christopher B., Couper, David J., Doerschuk, Claire M., Dransfield, Mark T., Han, MeiLan K., Hansel, Nadia N., Hastie, Annette T., Hoffman, Eric A., Kaner, Robert J., Krishnan, Jerry, O’Neal, Wanda K., Ortega, Victor E., Paine, Robert, Peters, Stephen P., Michael Wells, J., Woodruff, Prescott G., Martinez, Fernando J., Curtis, Jeffrey L., Huffnagle, Gary B., Huang, Yvonne J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865064/
https://www.ncbi.nlm.nih.gov/pubmed/33547327
http://dx.doi.org/10.1038/s41522-021-00185-9
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author Opron, Kristopher
Begley, Lesa A.
Erb-Downward, John R.
Freeman, Christine
Madapoosi, Siddharth
Alexis, Neil E.
Barjaktarevic, Igor
Graham Barr, R.
Bleecker, Eugene R.
Bowler, Russell P.
Christenson, Stephanie A.
Comellas, Alejandro P.
Cooper, Christopher B.
Couper, David J.
Doerschuk, Claire M.
Dransfield, Mark T.
Han, MeiLan K.
Hansel, Nadia N.
Hastie, Annette T.
Hoffman, Eric A.
Kaner, Robert J.
Krishnan, Jerry
O’Neal, Wanda K.
Ortega, Victor E.
Paine, Robert
Peters, Stephen P.
Michael Wells, J.
Woodruff, Prescott G.
Martinez, Fernando J.
Curtis, Jeffrey L.
Huffnagle, Gary B.
Huang, Yvonne J.
author_facet Opron, Kristopher
Begley, Lesa A.
Erb-Downward, John R.
Freeman, Christine
Madapoosi, Siddharth
Alexis, Neil E.
Barjaktarevic, Igor
Graham Barr, R.
Bleecker, Eugene R.
Bowler, Russell P.
Christenson, Stephanie A.
Comellas, Alejandro P.
Cooper, Christopher B.
Couper, David J.
Doerschuk, Claire M.
Dransfield, Mark T.
Han, MeiLan K.
Hansel, Nadia N.
Hastie, Annette T.
Hoffman, Eric A.
Kaner, Robert J.
Krishnan, Jerry
O’Neal, Wanda K.
Ortega, Victor E.
Paine, Robert
Peters, Stephen P.
Michael Wells, J.
Woodruff, Prescott G.
Martinez, Fernando J.
Curtis, Jeffrey L.
Huffnagle, Gary B.
Huang, Yvonne J.
author_sort Opron, Kristopher
collection PubMed
description Chronic obstructive pulmonary disease (COPD) is heterogeneous in development, progression, and phenotypes. Little is known about the lung microbiome, sampled by bronchoscopy, in milder COPD and its relationships to clinical features that reflect disease heterogeneity (lung function, symptom burden, and functional impairment). Using bronchoalveolar lavage fluid collected from 181 never-smokers and ever-smokers with or without COPD (GOLD 0-2) enrolled in the SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS), we find that lung bacterial composition associates with several clinical features, in particular bronchodilator responsiveness, peak expiratory flow rate, and forced expiratory flow rate between 25 and 75% of FVC (FEF(25–75)). Measures of symptom burden (COPD Assessment Test) and functional impairment (six-minute walk distance) also associate with disparate lung microbiota composition. Drivers of these relationships include members of the Streptococcus, Prevotella, Veillonella, Staphylococcus, and Pseudomonas genera. Thus, lung microbiota differences may contribute to airway dysfunction and airway disease in milder COPD.
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spelling pubmed-78650642021-02-11 Lung microbiota associations with clinical features of COPD in the SPIROMICS cohort Opron, Kristopher Begley, Lesa A. Erb-Downward, John R. Freeman, Christine Madapoosi, Siddharth Alexis, Neil E. Barjaktarevic, Igor Graham Barr, R. Bleecker, Eugene R. Bowler, Russell P. Christenson, Stephanie A. Comellas, Alejandro P. Cooper, Christopher B. Couper, David J. Doerschuk, Claire M. Dransfield, Mark T. Han, MeiLan K. Hansel, Nadia N. Hastie, Annette T. Hoffman, Eric A. Kaner, Robert J. Krishnan, Jerry O’Neal, Wanda K. Ortega, Victor E. Paine, Robert Peters, Stephen P. Michael Wells, J. Woodruff, Prescott G. Martinez, Fernando J. Curtis, Jeffrey L. Huffnagle, Gary B. Huang, Yvonne J. NPJ Biofilms Microbiomes Article Chronic obstructive pulmonary disease (COPD) is heterogeneous in development, progression, and phenotypes. Little is known about the lung microbiome, sampled by bronchoscopy, in milder COPD and its relationships to clinical features that reflect disease heterogeneity (lung function, symptom burden, and functional impairment). Using bronchoalveolar lavage fluid collected from 181 never-smokers and ever-smokers with or without COPD (GOLD 0-2) enrolled in the SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS), we find that lung bacterial composition associates with several clinical features, in particular bronchodilator responsiveness, peak expiratory flow rate, and forced expiratory flow rate between 25 and 75% of FVC (FEF(25–75)). Measures of symptom burden (COPD Assessment Test) and functional impairment (six-minute walk distance) also associate with disparate lung microbiota composition. Drivers of these relationships include members of the Streptococcus, Prevotella, Veillonella, Staphylococcus, and Pseudomonas genera. Thus, lung microbiota differences may contribute to airway dysfunction and airway disease in milder COPD. Nature Publishing Group UK 2021-02-05 /pmc/articles/PMC7865064/ /pubmed/33547327 http://dx.doi.org/10.1038/s41522-021-00185-9 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Opron, Kristopher
Begley, Lesa A.
Erb-Downward, John R.
Freeman, Christine
Madapoosi, Siddharth
Alexis, Neil E.
Barjaktarevic, Igor
Graham Barr, R.
Bleecker, Eugene R.
Bowler, Russell P.
Christenson, Stephanie A.
Comellas, Alejandro P.
Cooper, Christopher B.
Couper, David J.
Doerschuk, Claire M.
Dransfield, Mark T.
Han, MeiLan K.
Hansel, Nadia N.
Hastie, Annette T.
Hoffman, Eric A.
Kaner, Robert J.
Krishnan, Jerry
O’Neal, Wanda K.
Ortega, Victor E.
Paine, Robert
Peters, Stephen P.
Michael Wells, J.
Woodruff, Prescott G.
Martinez, Fernando J.
Curtis, Jeffrey L.
Huffnagle, Gary B.
Huang, Yvonne J.
Lung microbiota associations with clinical features of COPD in the SPIROMICS cohort
title Lung microbiota associations with clinical features of COPD in the SPIROMICS cohort
title_full Lung microbiota associations with clinical features of COPD in the SPIROMICS cohort
title_fullStr Lung microbiota associations with clinical features of COPD in the SPIROMICS cohort
title_full_unstemmed Lung microbiota associations with clinical features of COPD in the SPIROMICS cohort
title_short Lung microbiota associations with clinical features of COPD in the SPIROMICS cohort
title_sort lung microbiota associations with clinical features of copd in the spiromics cohort
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865064/
https://www.ncbi.nlm.nih.gov/pubmed/33547327
http://dx.doi.org/10.1038/s41522-021-00185-9
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