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Biomarkers of early chronic obstructive pulmonary disease (COPD) in smokers and former smokers. Protocol of a longitudinal study
BACKGROUND: Chronic obstructive pulmonary disease (COPD) is an irreversible disease, diagnosed predominantly in smokers. COPD is currently the third leading cause of death worldwide. Far more than 15 % of smokers get COPD: in fact, most develop some amount of pulmonary impairment. Smoking-related CO...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4781824/ https://www.ncbi.nlm.nih.gov/pubmed/26951192 http://dx.doi.org/10.1186/s40169-016-0086-5 |
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author | Truedsson, Mikael Malm, Johan Barbara Sahlin, K. Bugge, May Wieslander, Elisabet Dahlbäck, Magnus Appelqvist, Roger Fehniger, Thomas E. Marko-Varga, György |
author_facet | Truedsson, Mikael Malm, Johan Barbara Sahlin, K. Bugge, May Wieslander, Elisabet Dahlbäck, Magnus Appelqvist, Roger Fehniger, Thomas E. Marko-Varga, György |
author_sort | Truedsson, Mikael |
collection | PubMed |
description | BACKGROUND: Chronic obstructive pulmonary disease (COPD) is an irreversible disease, diagnosed predominantly in smokers. COPD is currently the third leading cause of death worldwide. Far more than 15 % of smokers get COPD: in fact, most develop some amount of pulmonary impairment. Smoking-related COPD is associated with both acute exacerbations and is closely correlated to comorbidities, such as cardiovascular disease and lung cancer. The objective of our study (KOL-Örestad) is to identify biomarkers in smokers and ex-smokers, with early signs of COPD, and compare these biomarkers with those of non-smokers and healthy smokers/ex-smokers. The participants in the study are recruited from Örestadskliniken, a primary health care clinic in Malmö, Sweden. METHODS: Two hundred smokers and ex-smokers diagnosed with COPD with airflow restriction according to GOLD stages 1–4 will be included and compared with 50 healthy never-smokers, and 50 healthy smokers/ex-smokers without airflow restriction (total n = 300). The age distribution is 35–80 years. The participants undergo a health examination including medical history, smoking history, lung function measurements, and respond to a “Quality of Life” questionnaire. Blood samples are drawn every 6 months during a period of 5 years. Additional blood sample collection is performed if participants are experiencing an exacerbation. The blood fractions will be analyzed by standard clinical chemistry assays and by proteomics utilizing mass spectrometry platforms. Optimal sample integrity is ensured by rapid handling with robotic biobank processing followed by storage at −80 °C. The study has been approved by the Regional Ethical Review Board in Lund (http://epn.se/en), (Approval number: DNR 2013/480), and registered at the NIH clinical trial registry (http://clinicaltrials.gov). RESULTS AND DISCUSSION: Currently, 220 subjects are enrolled in the study. CONCLUSIONS AND FUTURE DIRECTIONS: The study design will enable discovery of new biomarkers by using novel mass spectrometric techniques that define early changes of COPD. Such panels of novel biomarkers may be able to distinguish COPD from closely related diseases, co-morbidities, and contribute to an increased understanding of these diseases. [Figure: see text] |
format | Online Article Text |
id | pubmed-4781824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-47818242016-04-09 Biomarkers of early chronic obstructive pulmonary disease (COPD) in smokers and former smokers. Protocol of a longitudinal study Truedsson, Mikael Malm, Johan Barbara Sahlin, K. Bugge, May Wieslander, Elisabet Dahlbäck, Magnus Appelqvist, Roger Fehniger, Thomas E. Marko-Varga, György Clin Transl Med Research BACKGROUND: Chronic obstructive pulmonary disease (COPD) is an irreversible disease, diagnosed predominantly in smokers. COPD is currently the third leading cause of death worldwide. Far more than 15 % of smokers get COPD: in fact, most develop some amount of pulmonary impairment. Smoking-related COPD is associated with both acute exacerbations and is closely correlated to comorbidities, such as cardiovascular disease and lung cancer. The objective of our study (KOL-Örestad) is to identify biomarkers in smokers and ex-smokers, with early signs of COPD, and compare these biomarkers with those of non-smokers and healthy smokers/ex-smokers. The participants in the study are recruited from Örestadskliniken, a primary health care clinic in Malmö, Sweden. METHODS: Two hundred smokers and ex-smokers diagnosed with COPD with airflow restriction according to GOLD stages 1–4 will be included and compared with 50 healthy never-smokers, and 50 healthy smokers/ex-smokers without airflow restriction (total n = 300). The age distribution is 35–80 years. The participants undergo a health examination including medical history, smoking history, lung function measurements, and respond to a “Quality of Life” questionnaire. Blood samples are drawn every 6 months during a period of 5 years. Additional blood sample collection is performed if participants are experiencing an exacerbation. The blood fractions will be analyzed by standard clinical chemistry assays and by proteomics utilizing mass spectrometry platforms. Optimal sample integrity is ensured by rapid handling with robotic biobank processing followed by storage at −80 °C. The study has been approved by the Regional Ethical Review Board in Lund (http://epn.se/en), (Approval number: DNR 2013/480), and registered at the NIH clinical trial registry (http://clinicaltrials.gov). RESULTS AND DISCUSSION: Currently, 220 subjects are enrolled in the study. CONCLUSIONS AND FUTURE DIRECTIONS: The study design will enable discovery of new biomarkers by using novel mass spectrometric techniques that define early changes of COPD. Such panels of novel biomarkers may be able to distinguish COPD from closely related diseases, co-morbidities, and contribute to an increased understanding of these diseases. [Figure: see text] Springer Berlin Heidelberg 2016-03-07 /pmc/articles/PMC4781824/ /pubmed/26951192 http://dx.doi.org/10.1186/s40169-016-0086-5 Text en © Truedsson et al. 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. |
spellingShingle | Research Truedsson, Mikael Malm, Johan Barbara Sahlin, K. Bugge, May Wieslander, Elisabet Dahlbäck, Magnus Appelqvist, Roger Fehniger, Thomas E. Marko-Varga, György Biomarkers of early chronic obstructive pulmonary disease (COPD) in smokers and former smokers. Protocol of a longitudinal study |
title | Biomarkers of early chronic obstructive pulmonary disease (COPD) in smokers and former smokers. Protocol of a longitudinal study |
title_full | Biomarkers of early chronic obstructive pulmonary disease (COPD) in smokers and former smokers. Protocol of a longitudinal study |
title_fullStr | Biomarkers of early chronic obstructive pulmonary disease (COPD) in smokers and former smokers. Protocol of a longitudinal study |
title_full_unstemmed | Biomarkers of early chronic obstructive pulmonary disease (COPD) in smokers and former smokers. Protocol of a longitudinal study |
title_short | Biomarkers of early chronic obstructive pulmonary disease (COPD) in smokers and former smokers. Protocol of a longitudinal study |
title_sort | biomarkers of early chronic obstructive pulmonary disease (copd) in smokers and former smokers. protocol of a longitudinal study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4781824/ https://www.ncbi.nlm.nih.gov/pubmed/26951192 http://dx.doi.org/10.1186/s40169-016-0086-5 |
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