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Serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations
BACKGROUND: Bilirubin is a potent anti-oxidant and higher serum concentrations of bilirubin have been associated with better lung function, slower lung function decline, and lower incidence of chronic obstructive pulmonary disease (COPD). We sought to determine whether elevated bilirubin blood conce...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655988/ https://www.ncbi.nlm.nih.gov/pubmed/29065885 http://dx.doi.org/10.1186/s12931-017-0664-0 |
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author | Brown, Kirstin E. Sin, Don D. Voelker, Helen Connett, John E. Niewoehner, Dennis E. Kunisaki, Ken M. |
author_facet | Brown, Kirstin E. Sin, Don D. Voelker, Helen Connett, John E. Niewoehner, Dennis E. Kunisaki, Ken M. |
author_sort | Brown, Kirstin E. |
collection | PubMed |
description | BACKGROUND: Bilirubin is a potent anti-oxidant and higher serum concentrations of bilirubin have been associated with better lung function, slower lung function decline, and lower incidence of chronic obstructive pulmonary disease (COPD). We sought to determine whether elevated bilirubin blood concentrations are associated with lower risk for acute exacerbations of COPD (AECOPD). METHODS: We performed a secondary analyses of data in the Simvastatin for Prevention of Exacerbations in Moderate-to-Severe COPD (STATCOPE) and the Azithromycin for Prevention of Exacerbations of COPD (MACRO) studies. We used time-dependent multivariable Cox proportional hazards analyses, using bilirubin concentrations prior to first AECOPD as the exposure variable and time to first AECOPD as the outcome variable. STATCOPE was used for model development, with validation in MACRO. RESULTS: In STATCOPE (n = 853), higher bilirubin was associated with a lower but statistically insignificant hazard for AECOPD, (adjusted hazard ratio [aHR] 0.89 per log(10) increase [95%CI: 0.74 to 1.09; p = 0.26]). In the validation MACRO study (n = 1018), higher bilirubin was associated with a significantly lower hazard for AECOPD (aHR 0.80 per log(10) increase [95%CI: 0.67 to 0.94; p = 0.008]). CONCLUSIONS: Bilirubin may be a biomarker of AECOPD risk and may be a novel therapeutic target to reduce AECOPD risk. TRIAL REGISTRATIONS: ClinicalTrials.gov NCT01061671 (registered 02 February 2010) and ClinicalTrials.gov NCT00325897 (registered 12 May 2006). |
format | Online Article Text |
id | pubmed-5655988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56559882017-10-31 Serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations Brown, Kirstin E. Sin, Don D. Voelker, Helen Connett, John E. Niewoehner, Dennis E. Kunisaki, Ken M. Respir Res Research BACKGROUND: Bilirubin is a potent anti-oxidant and higher serum concentrations of bilirubin have been associated with better lung function, slower lung function decline, and lower incidence of chronic obstructive pulmonary disease (COPD). We sought to determine whether elevated bilirubin blood concentrations are associated with lower risk for acute exacerbations of COPD (AECOPD). METHODS: We performed a secondary analyses of data in the Simvastatin for Prevention of Exacerbations in Moderate-to-Severe COPD (STATCOPE) and the Azithromycin for Prevention of Exacerbations of COPD (MACRO) studies. We used time-dependent multivariable Cox proportional hazards analyses, using bilirubin concentrations prior to first AECOPD as the exposure variable and time to first AECOPD as the outcome variable. STATCOPE was used for model development, with validation in MACRO. RESULTS: In STATCOPE (n = 853), higher bilirubin was associated with a lower but statistically insignificant hazard for AECOPD, (adjusted hazard ratio [aHR] 0.89 per log(10) increase [95%CI: 0.74 to 1.09; p = 0.26]). In the validation MACRO study (n = 1018), higher bilirubin was associated with a significantly lower hazard for AECOPD (aHR 0.80 per log(10) increase [95%CI: 0.67 to 0.94; p = 0.008]). CONCLUSIONS: Bilirubin may be a biomarker of AECOPD risk and may be a novel therapeutic target to reduce AECOPD risk. TRIAL REGISTRATIONS: ClinicalTrials.gov NCT01061671 (registered 02 February 2010) and ClinicalTrials.gov NCT00325897 (registered 12 May 2006). BioMed Central 2017-10-24 2017 /pmc/articles/PMC5655988/ /pubmed/29065885 http://dx.doi.org/10.1186/s12931-017-0664-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 Brown, Kirstin E. Sin, Don D. Voelker, Helen Connett, John E. Niewoehner, Dennis E. Kunisaki, Ken M. Serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations |
title | Serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations |
title_full | Serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations |
title_fullStr | Serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations |
title_full_unstemmed | Serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations |
title_short | Serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations |
title_sort | serum bilirubin and the risk of chronic obstructive pulmonary disease exacerbations |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655988/ https://www.ncbi.nlm.nih.gov/pubmed/29065885 http://dx.doi.org/10.1186/s12931-017-0664-0 |
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