Increased systemic inflammation is a risk factor for COPD exacerbations

被引:132
作者
Groenewegen, Karin H. [1 ]
Postma, Dirkje S. [2 ]
Hop, Wim C. J. [3 ]
Wielders, Pascal L. M. L. [4 ]
Schlosser, Noel J. J. [5 ]
Wouters, Entiel F. M. [1 ]
机构
[1] Univ Hosp Maastricht, Dept Resp Med, NL-6202 AZ Maastricht, Netherlands
[2] Univ Groningen, Univ Med Ctr, Groningen, Netherlands
[3] Erasmus MC, Dept Epidemiol & Biostat, Rotterdam, Netherlands
[4] Catharina Hosp Einhoven, Dept Resp Med, Eindhoven, Netherlands
[5] Cent Mil Hosp Utrecht, Dept Resp Med, Utrecht, Netherlands
关键词
acute exacerbation; COPD; systemic inflammation;
D O I
10.1378/chest.07-1342
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: COPD is characterized by episodic increases in respiratory symptoms, so-called exacerbations. COPD exacerbations are associated with an increase in local and systemic inflammation. Data of a previously published study in a well-characterized COPD cohort were analyzed to define predictive factors of acute exacerbations, particularly focusing on systemic inflammation. Objective: To determine if an elevated systemic inflammatory status measured at baseline is related to the occurrence of acute exacerbations in patients with COPD. Methods: The occurrence of moderate (requiring oral prednisolone) and severe exacerbations (requiring hospitalization) was prospectively recorded over 1 year. At the beginning of the study, lung function values (FEV1, FVC, functional residual capacity, and diffusion capacity of the lung for carbon monoxide [DLCO]) and serum levels of C-reactive protein, fibrinogen, lipopolysaccharide binding protein, tumor necrosis factor (TNF)-alpha, and its soluble receptors (soluble TNF receptors 55 and 75) as markers of systemic inflammation were determined. Results: Two hundred seventy-seven person-years of follow-up were analyzed in the total group of 314 patients: 186 patients were responsible for 411 exacerbations (374 moderate and 37 severe). Multivariate analyses showed that a higher initial fibrinogen level and a lower FEV1 predicted a higher rate of both moderate and severe exacerbations. Additional independent predictors of a severe exacerbation were a higher number of prestudy severe exacerbations and lower DLCO. A higher number of prestudy moderate exacerbations was the only additional independent risk factor for the rate of moderate exacerbations. Conclusion: This study demonstrates that besides lung function impairment systemic inflammation manifested by elevated fibrinogen levels is an independent risk factor for exacerbations of COPD. Attenuation of systemic inflammation may offer new perspectives in the management of COPD patients to reduce the burden of exacerbations.
引用
收藏
页码:350 / 357
页数:8
相关论文
共 38 条
  • [1] Elevated plasma procoagulant and fibrinolytic markers in patients with chronic obstructive pulmonary disease
    Ashitani, J
    Mukae, H
    Arimura, Y
    Matsukura, S
    [J]. INTERNAL MEDICINE, 2002, 41 (03) : 181 - 185
  • [2] Outcomes following acute exacerbation of severe chronic obstructive lung disease
    Connors, AF
    Dawson, NV
    Thomas, C
    Harrell, FE
    Desbiens, N
    Fulkerson, WJ
    Kussin, P
    Bellamy, P
    Goldman, L
    Knaus, WA
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (04) : 959 - 967
  • [3] STANDARDIZATION OF THE MEASUREMENT OF TRANSFER-FACTOR (DIFFUSING-CAPACITY) - REPORT WORKING PARTY STANDARDIZATION OF LUNG-FUNCTION TESTS EUROPEAN-COMMUNITY FOR STEEL AND COAL - OFFICIAL STATEMENT OF THE EUROPEAN RESPIRATORY SOCIETY
    COTES, JE
    CHINN, DJ
    QUANJER, PH
    ROCA, J
    YERNAULT, JC
    [J]. EUROPEAN RESPIRATORY JOURNAL, 1993, 6 : 41 - 52
  • [4] Elevated plasma fibrinogen associated with reduced pulmonary function and increased risk of chronic obstructive pulmonary disease
    Dahl, M
    Tybjærg-Hansen, A
    Vestbo, J
    Lange, P
    Nordestgaard, BG
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 164 (06) : 1008 - 1011
  • [5] Plasma fibrinogen level and the risk of major cardiovascular diseases and nonvascular mortality - An individual participant meta-analysis
    Danesh, J
    Lewington, S
    Thompson, SG
    Lowe, GDO
    Collins, R
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 294 (14): : 1799 - 1809
  • [6] Enhanced thromboxane biosynthesis in patients with chronic obstructive pulmonary disease
    Davi, G
    Basili, S
    Vieri, M
    Cipollone, F
    Santarone, S
    Alessandri, C
    Gazzaniga, P
    Cordova, C
    Violi, F
    DeLuca, N
    Coppotelli, L
    Paradiso, M
    Bellomo, A
    Belogi, A
    Ferroni, P
    Pulcinelli, F
    Roccaforte, S
    Antidormi, T
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (06) : 1794 - 1799
  • [7] Systemic anti-inflammatory mediators in COPD: increase in soluble interleukin 1 receptor II during treatment of exacerbations
    Dentener, MA
    Creutzberg, EC
    Schols, AMWJ
    Mantovani, A
    van't Veer, C
    Buurman, WA
    Wouters, EFM
    [J]. THORAX, 2001, 56 (09) : 721 - 726
  • [8] Value of C-reactive protein measurements in exacerbations of chronic obstructive pulmonary disease
    Dev, D
    Wallace, E
    Sankaran, R
    Cunniffe, J
    Govan, JRW
    Wathen, CG
    Emmanuel, FXS
    [J]. RESPIRATORY MEDICINE, 1998, 92 (04) : 664 - 667
  • [9] Airway and systemic inflammation and decline in lung function in patients with COPD
    Donaldson, GC
    Seemungal, TAR
    Patel, IS
    Bhowmik, A
    Wilkinson, TMA
    Hurst, JR
    MacCallum, PK
    Wedzicha, JA
    [J]. CHEST, 2005, 128 (04) : 1995 - 2004
  • [10] Exacerbations and time spent outdoors in chronic obstructive pulmonary disease
    Donaldson, GC
    Wilkinson, TMA
    Hurst, JR
    Perera, WR
    Wedzicha, JA
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 171 (05) : 446 - 452