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Respir Res. 2015 Jun 11;16:69. doi: 10.1186/s12931-015-0225-3.

Accelerated extracellular matrix turnover during exacerbations of COPD.

Author information

1
Nordic Bioscience, Biomarkers and Research, Herlev Hovedgade 207, 2730, Herlev, Denmark. jsa@nordicbioscience.com.
2
Section of Social Medicine, Institute of Public Health, University of Copenhagen, Oester Farimagsgade 5, 1014, Copenhagen K, Denmark. jsa@nordicbioscience.com.
3
Division of Respiratory Medicine and Nottingham Respiratory Research Unit, University of Nottingham, Hucknall Road, Nottingham, NG5 1 PB, UK. alan.knox@nottingham.ac.uk.
4
Section of Social Medicine, Institute of Public Health, University of Copenhagen, Oester Farimagsgade 5, 1014, Copenhagen K, Denmark. peter.lange@sund.ku.dk.
5
Section of Respiratory Medicine, Hvidovre Hospital, Kettegaards Alle 30, 2650, Hvidovre, Denmark. peter.lange@sund.ku.dk.
6
Nordic Bioscience, Biomarkers and Research, Herlev Hovedgade 207, 2730, Herlev, Denmark. ssu@nordicbioscience.com.
7
Nordic Bioscience, Biomarkers and Research, Herlev Hovedgade 207, 2730, Herlev, Denmark. jhk@nordicbioscience.com.
8
Nordic Bioscience, Biomarkers and Research, Herlev Hovedgade 207, 2730, Herlev, Denmark. djl@nordicbioscience.com.
9
Nordic Bioscience, Biomarkers and Research, Herlev Hovedgade 207, 2730, Herlev, Denmark. mk@nordicbioscience.com.
10
Division of Respiratory Medicine and Nottingham Respiratory Research Unit, University of Nottingham, Hucknall Road, Nottingham, NG5 1 PB, UK. charlotte.bolton@nottingham.ac.uk.
11
Division of Respiratory Medicine and Nottingham Respiratory Research Unit, University of Nottingham, Hucknall Road, Nottingham, NG5 1 PB, UK. simon.johnson@nottingham.ac.uk.

Abstract

BACKGROUND:

Exacerbations of chronic obstructive pulmonary disease (COPD) contribute significantly to disease progression. However, the effect on tissue structure and turnover is not well described. There is an urgent clinical need for biomarkers of disease activity associated with disease progression. Extracellular matrix (ECM) turnover reflects activity in tissues and consequently assessment of ECM turnover may serve as biomarkers of disease activity. We hypothesized that the turnover of lung ECM proteins were altered during exacerbations of COPD.

METHODS:

69 patients with COPD hospitalised for an exacerbation were recruited at admission and returned for a 4 weeks follow-up. Competitive ELISAs measuring circulating protein fragments in serum or plasma assessed the formation and degradation of collagen types III (Pro-C3 and C3M, respectively), IV (P4NP 7S and C4M, respectively), and VI (Pro-C6 and C6M, respectively), and degradation of elastin (ELM7 and EL-NE) and versican (VCANM).

RESULTS:

Circulating levels of C3M, C4M, C6M, ELM7, and EL-NE were elevated during an exacerbation of COPD as compared to follow-up (all P <0.0001), while VCANM levels were decreased (P <0.0001). Pro-C6 levels were decreased and P4NP 7S levels were elevated during exacerbation (P <0.0001). Pro-C3 levels were unchanged. At time of exacerbation, degradation/formation ratios were increased for collagen types III and VI and decreased for collagen type IV.

CONCLUSIONS:

Exacerbations of COPD resulted in elevated levels of circulating fragments of structural proteins, which may serve as markers of disease activity. This suggests that patients with COPD have accelerated ECM turnover during exacerbations which may be related to disease progression.

PMID:
26062683
PMCID:
PMC4491243
DOI:
10.1186/s12931-015-0225-3
[Indexed for MEDLINE]
Free PMC Article

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