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Tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease
INTRODUCTION: Exacerbations are a leading cause of morbidity in COPD. The objective of this study was to identify metabolomic biomarkers of acute exacerbations of COPD (AECOPD). METHODS: We measured metabolites via mass spectrometry (MS) in plasma drawn within 24 hours of admission to the hospital f...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047709/ https://www.ncbi.nlm.nih.gov/pubmed/27729784 http://dx.doi.org/10.2147/COPD.S107844 |
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author | Gulcev, Makedonka Reilly, Cavan Griffin, Timothy J Broeckling, Corey D Sandri, Brian J Witthuhn, Bruce A Hodgson, Shane W Woodruff, Prescott G Wendt, Chris H |
author_facet | Gulcev, Makedonka Reilly, Cavan Griffin, Timothy J Broeckling, Corey D Sandri, Brian J Witthuhn, Bruce A Hodgson, Shane W Woodruff, Prescott G Wendt, Chris H |
author_sort | Gulcev, Makedonka |
collection | PubMed |
description | INTRODUCTION: Exacerbations are a leading cause of morbidity in COPD. The objective of this study was to identify metabolomic biomarkers of acute exacerbations of COPD (AECOPD). METHODS: We measured metabolites via mass spectrometry (MS) in plasma drawn within 24 hours of admission to the hospital for 33 patients with an AECOPD (day 0) and 30 days later and for 65 matched controls. Individual metabolites were measured via selective reaction monitoring with mass spectrometry. We used a mixed-effect model to compare metabolite levels in cases compared to controls and a paired t-test to test for differences between days 0 and 30 in the AECOPD group. RESULTS: We identified 377 analytes at a false discovery rate of 5% that differed between cases (day 0) and controls, and 31 analytes that differed in the AECOPD cases between day 0 and day 30 (false discovery rate: 5%). Tryptophan was decreased at day 0 of AECOPD compared to controls corresponding to an increase in indoleamine 2,3-dioxygenase activity. CONCLUSION: Patients with AECOPD have a unique metabolomic signature that includes a decrease in tryptophan levels consistent with an increase in indoleamine 2,3-dioxygenase activity. |
format | Online Article Text |
id | pubmed-5047709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50477092016-10-11 Tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease Gulcev, Makedonka Reilly, Cavan Griffin, Timothy J Broeckling, Corey D Sandri, Brian J Witthuhn, Bruce A Hodgson, Shane W Woodruff, Prescott G Wendt, Chris H Int J Chron Obstruct Pulmon Dis Original Research INTRODUCTION: Exacerbations are a leading cause of morbidity in COPD. The objective of this study was to identify metabolomic biomarkers of acute exacerbations of COPD (AECOPD). METHODS: We measured metabolites via mass spectrometry (MS) in plasma drawn within 24 hours of admission to the hospital for 33 patients with an AECOPD (day 0) and 30 days later and for 65 matched controls. Individual metabolites were measured via selective reaction monitoring with mass spectrometry. We used a mixed-effect model to compare metabolite levels in cases compared to controls and a paired t-test to test for differences between days 0 and 30 in the AECOPD group. RESULTS: We identified 377 analytes at a false discovery rate of 5% that differed between cases (day 0) and controls, and 31 analytes that differed in the AECOPD cases between day 0 and day 30 (false discovery rate: 5%). Tryptophan was decreased at day 0 of AECOPD compared to controls corresponding to an increase in indoleamine 2,3-dioxygenase activity. CONCLUSION: Patients with AECOPD have a unique metabolomic signature that includes a decrease in tryptophan levels consistent with an increase in indoleamine 2,3-dioxygenase activity. Dove Medical Press 2016-09-29 /pmc/articles/PMC5047709/ /pubmed/27729784 http://dx.doi.org/10.2147/COPD.S107844 Text en © 2016 Gulcev et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Gulcev, Makedonka Reilly, Cavan Griffin, Timothy J Broeckling, Corey D Sandri, Brian J Witthuhn, Bruce A Hodgson, Shane W Woodruff, Prescott G Wendt, Chris H Tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease |
title | Tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease |
title_full | Tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease |
title_fullStr | Tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease |
title_full_unstemmed | Tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease |
title_short | Tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease |
title_sort | tryptophan catabolism in acute exacerbations of chronic obstructive pulmonary disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047709/ https://www.ncbi.nlm.nih.gov/pubmed/27729784 http://dx.doi.org/10.2147/COPD.S107844 |
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