Inhaled Steroids Modulate Extracellular Matrix Composition in Bronchial Biopsies of COPD Patients: A Randomized, Controlled Trial

被引:16
作者
Kunz, Lisette I. Z. [1 ]
Strebus, Jolanda [1 ]
Budulac, Simona E. [2 ]
Lapperre, Therese S. [1 ]
Sterk, Peter J. [3 ]
Postma, Dirkje S. [4 ]
Mauad, Thais [5 ]
Timens, Wim [6 ]
Hiemstra, Pieter S. [1 ]
机构
[1] Leiden Univ Med Ctr, Dept Pulmonol, Leiden, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Resp Med, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Pulmonol, Groningen, Netherlands
[5] Univ Sao Paulo, Sch Med, Dept Pathol, Sao Paulo, Brazil
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol, Groningen, Netherlands
来源
PLOS ONE | 2013年 / 8卷 / 05期
关键词
OBSTRUCTIVE PULMONARY-DISEASE; FIBROBLAST PROTEOGLYCAN PRODUCTION; GENE-EXPRESSION; CIGARETTE-SMOKE; PATHOGENESIS; ELASTIN; TISSUE; AIRWAY; MACROPHAGES; ALVEOLI;
D O I
10.1371/journal.pone.0063430
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rationale: Smoking and inflammation contribute to the pathogenesis of chronic obstructive pulmonary disease (COPD), which involves changes in extracellular matrix. This is thought to contribute to airway remodeling and airflow obstruction. We have previously observed that long-term treatment with inhaled corticosteroids can not only reduce bronchial inflammation, but can also attenuate lung function decline in moderate-severe COPD. We hypothesized that inhaled corticosteroids and current smoking modulate bronchial extracellular matrix components in COPD. Objective: To compare major extracellular matrix components (elastic fibers; proteoglycans [versican, decorin]; collagens type I and III) in bronchial biopsies 1) after 30-months inhaled steroids treatment or placebo; and 2) between current and exsmokers with COPD. Methods: We included 64 moderate-severe, steroid-naive COPD patients (24/40 (ex)-smokers, 62 +/- 7 years, 46 (31-54) packyears, post-bronchodilator forced expiratory volume in one second (FEV1) 62 +/- 9% predicted) at baseline in this randomized, controlled trial. 19 and 13 patients received 30-months treatment with fluticasone or placebo, respectively. Bronchial biopsies collected at baseline and after 30 months were studied using (immuno) histochemistry to evaluate extracellular matrix content. Percentage and density of stained area were calculated by digital image analysis. Results: 30-Months inhaled steroids increased the percentage stained area of versican (9.6% [CI 0.9 to 18.3%]; p = 0.03) and collagen III (20.6% [CI 3.8 to 37.4%]; p = 0.02) compared to placebo. Increased collagen I staining density correlated with increased post-bronchodilator FEV1 after inhaled steroids treatment (Rs = 0.45, p = 0.04). There were no differences between smokers and ex-smokers with COPD in percentages and densities for all extracellular matrix proteins. Conclusions: These data show that long-term inhaled corticosteroids treatment partially changes the composition of extracellular matrix in moderate-severe COPD. This is associated with increased lung function, suggesting that long-term inhaled steroids modulate airway remodeling thereby potentially preventing airway collapse in COPD. Smoking status is not associated with bronchial extracellular matrix proteins.
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页数:8
相关论文
共 34 条
[1]   Extracellular matrix composition in COPD [J].
Annoni, Raquel ;
Lancas, Tatiana ;
Tanigawa, Ryan Yukimatsu ;
Matsushita, Marcus de Medeiros ;
Fernezlian, Sandra de Morais ;
Bruno, Andreina ;
Ferraz da Silva, Luiz Fernando ;
Roughley, Peter J. ;
Battaglia, Salvatore ;
Dolhnikoff, Marisa ;
Hiemstra, Pieter S. ;
Sterk, Peter J. ;
Rabe, Klaus F. ;
Mauad, Thais .
EUROPEAN RESPIRATORY JOURNAL, 2012, 40 (06) :1362-1373
[2]   Changes in elastic fibres in the small airways and alveoli in COPD [J].
Black, P. N. ;
Ching, P. S. T. ;
Beaumont, B. ;
Ranasinghe, S. ;
Taylor, G. ;
Merrilees, M. J. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 31 (05) :998-1004
[3]   Chronic Obstructive Pulmonary Disease 1 New insights into the immunology of chronic obstructive pulmonary disease [J].
Brusselle, Guy G. ;
Joos, Guy F. ;
Bracke, Ken R. .
LANCET, 2011, 378 (9795) :1015-1026
[4]   Multidrug resistance-associated protein-1 (MRP1) genetic variants, MRP1 protein levels and severity of COPD [J].
Budulac, Simona E. ;
Postma, Dirkje S. ;
Hiemstra, Pieter S. ;
Kunz, Lisette I. Z. ;
Siedlinski, Mateusz ;
Smit, Henriette A. ;
Vonk, Judith M. ;
Rutgers, Bea ;
Timens, Wim ;
Boezen, H. Marike .
RESPIRATORY RESEARCH, 2010, 11
[5]   ELASTIN CONTENT OF NORMAL AND EMPHYSEMATOUS LUNG PARENCHYMA [J].
CHRZANOWSKI, P ;
KELLER, S ;
CERRETA, J ;
MANDL, I ;
TURINO, GM .
AMERICAN JOURNAL OF MEDICINE, 1980, 69 (03) :351-359
[6]   Expression of Profibrotic Mediators in Small Airways versus Parenchyma after Cigarette Smoke Exposure [J].
Churg, Andrew ;
Zhou, Steven ;
Preobrazhenska, Olena ;
Tai, Hsin ;
Wang, Rona ;
Wright, Joanne L. .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2009, 40 (03) :268-276
[7]   Elastin expression in very severe human COPD [J].
Deslee, G. ;
Woods, J. C. ;
Moore, C. M. ;
Liu, L. ;
Conradi, S. H. ;
Milne, M. ;
Gierada, D. S. ;
Pierce, J. ;
Patterson, A. ;
Lewit, R. A. ;
Battaile, J. T. ;
Holtzman, M. J. ;
Hogg, J. C. ;
Pierce, R. A. .
EUROPEAN RESPIRATORY JOURNAL, 2009, 34 (02) :324-331
[8]   Extracellular matrix, integrins, and mesenchymal cell function in the airways [J].
Fernandes, DJ ;
Bonacci, JV ;
Stewart, AG .
CURRENT DRUG TARGETS, 2006, 7 (05) :567-577
[9]   Transcriptional and posttranscriptional inhibition of lysyl oxidase expression by cigarette smoke condensate in cultured rat fetal lung fibroblasts [J].
Gao, S ;
Chen, KY ;
Zhao, YZ ;
Rich, CB ;
Chen, LJ ;
Li, SJ ;
Toselli, P ;
Stone, P ;
Li, WD .
TOXICOLOGICAL SCIENCES, 2005, 87 (01) :197-203
[10]  
GODFREY RWA, 1995, EUR RESPIR J, V8, P922