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High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD – results from the ECLIPSE study
BACKGROUND: There is a need to identify individuals with COPD at risk for disease progression and mortality. Lung tissue remodeling is associated with the release of extracellular matrix (ECM) fragments into the peripheral circulation. We hypothesized that ECM remodeling was associated with mortalit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050854/ https://www.ncbi.nlm.nih.gov/pubmed/27716343 http://dx.doi.org/10.1186/s12931-016-0440-6 |
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author | Sand, Jannie M. B. Leeming, Diana J. Byrjalsen, Inger Bihlet, Asger R. Lange, Peter Tal-Singer, Ruth Miller, Bruce E. Karsdal, Morten A. Vestbo, Jørgen |
author_facet | Sand, Jannie M. B. Leeming, Diana J. Byrjalsen, Inger Bihlet, Asger R. Lange, Peter Tal-Singer, Ruth Miller, Bruce E. Karsdal, Morten A. Vestbo, Jørgen |
author_sort | Sand, Jannie M. B. |
collection | PubMed |
description | BACKGROUND: There is a need to identify individuals with COPD at risk for disease progression and mortality. Lung tissue remodeling is associated with the release of extracellular matrix (ECM) fragments into the peripheral circulation. We hypothesized that ECM remodeling was associated with mortality in COPD and measured neo-epitopes originating from ECM proteins associated with lung tissue remodeling. METHODS: Biomarkers of ECM remodeling were assessed in a subpopulation (n = 1000) of the Evaluation of COPD Longitudinally to Identify Predictive Surrogate End-points (ECLIPSE) cohort. Validated immunoassays measuring serological neo-epitopes produced by proteolytic cleavage associated with degradation of collagen type I, III, IV, and VI, elastin, and biglycan, and formation of collagen type VI as well as fibrinogen and C-reactive protein were used. Multivariate models were used to assess the prognostic value of these biomarkers. RESULTS: Thirty subjects (3.0 %) died during follow-up. Non-survivors were older, had reduced exercise capacity, increased dyspnea score, and included fewer current smokers. All collagen biomarkers were significantly elevated in non-survivors compared to survivors. Mortality risk was significantly increased for subjects with collagen remodeling biomarkers in the upper quartile, especially for the degradation fragment of collagen type IV C6M (hazard ratio 6.6 [95 % confidence interval 2.9-15.2], P < 0.0001) after adjusting for relevant confounders. CONCLUSIONS: Serological biomarkers of collagen remodeling were strongly associated with mortality in subjects with COPD indicating that assessment of tissue turnover in the parenchyma and small airways may be useful in the prognosis of COPD. TRIAL REGISTRATION: NCT00292552, GSK Study No. SCO104960. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-016-0440-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5050854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50508542016-10-05 High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD – results from the ECLIPSE study Sand, Jannie M. B. Leeming, Diana J. Byrjalsen, Inger Bihlet, Asger R. Lange, Peter Tal-Singer, Ruth Miller, Bruce E. Karsdal, Morten A. Vestbo, Jørgen Respir Res Research BACKGROUND: There is a need to identify individuals with COPD at risk for disease progression and mortality. Lung tissue remodeling is associated with the release of extracellular matrix (ECM) fragments into the peripheral circulation. We hypothesized that ECM remodeling was associated with mortality in COPD and measured neo-epitopes originating from ECM proteins associated with lung tissue remodeling. METHODS: Biomarkers of ECM remodeling were assessed in a subpopulation (n = 1000) of the Evaluation of COPD Longitudinally to Identify Predictive Surrogate End-points (ECLIPSE) cohort. Validated immunoassays measuring serological neo-epitopes produced by proteolytic cleavage associated with degradation of collagen type I, III, IV, and VI, elastin, and biglycan, and formation of collagen type VI as well as fibrinogen and C-reactive protein were used. Multivariate models were used to assess the prognostic value of these biomarkers. RESULTS: Thirty subjects (3.0 %) died during follow-up. Non-survivors were older, had reduced exercise capacity, increased dyspnea score, and included fewer current smokers. All collagen biomarkers were significantly elevated in non-survivors compared to survivors. Mortality risk was significantly increased for subjects with collagen remodeling biomarkers in the upper quartile, especially for the degradation fragment of collagen type IV C6M (hazard ratio 6.6 [95 % confidence interval 2.9-15.2], P < 0.0001) after adjusting for relevant confounders. CONCLUSIONS: Serological biomarkers of collagen remodeling were strongly associated with mortality in subjects with COPD indicating that assessment of tissue turnover in the parenchyma and small airways may be useful in the prognosis of COPD. TRIAL REGISTRATION: NCT00292552, GSK Study No. SCO104960. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-016-0440-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-04 2016 /pmc/articles/PMC5050854/ /pubmed/27716343 http://dx.doi.org/10.1186/s12931-016-0440-6 Text en © The Author(s). 2016 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 Sand, Jannie M. B. Leeming, Diana J. Byrjalsen, Inger Bihlet, Asger R. Lange, Peter Tal-Singer, Ruth Miller, Bruce E. Karsdal, Morten A. Vestbo, Jørgen High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD – results from the ECLIPSE study |
title | High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD – results from the ECLIPSE study |
title_full | High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD – results from the ECLIPSE study |
title_fullStr | High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD – results from the ECLIPSE study |
title_full_unstemmed | High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD – results from the ECLIPSE study |
title_short | High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD – results from the ECLIPSE study |
title_sort | high levels of biomarkers of collagen remodeling are associated with increased mortality in copd – results from the eclipse study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050854/ https://www.ncbi.nlm.nih.gov/pubmed/27716343 http://dx.doi.org/10.1186/s12931-016-0440-6 |
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