Association between markers of emphysema and more severe chronic obstructive pulmonary disease

Background: The predominant emphysema phenotype is associated with more severe airflow limitation in patients with chronic obstructive pulmonary disease (COPD). A study was undertaken to investigate whether COPD patients, with or without emphysema quantitatively confirmed by high resolution computed...

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Published inThorax Vol. 61; no. 12; pp. 1037 - 1042
Main Authors Boschetto, P, Quintavalle, S, Zeni, E, Leprotti, S, Potena, A, Ballerin, L, Papi, A, Palladini, G, Luisetti, M, Annovazzi, L, Iadarola, P, De Rosa, E, Fabbri, L M, Mapp, C E
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd and British Thoracic Society 01.12.2006
BMJ
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ISSN0040-6376
1468-3296
DOI10.1136/thx.2006.058321

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Abstract Background: The predominant emphysema phenotype is associated with more severe airflow limitation in patients with chronic obstructive pulmonary disease (COPD). A study was undertaken to investigate whether COPD patients, with or without emphysema quantitatively confirmed by high resolution computed tomography (HRCT), have different COPD severity as assessed by the BODE index (body mass index, airflow obstruction, dyspnoea, exercise performance) and inspiratory capacity to total lung capacity ratio (IC/TLC), and by different biological markers of lung parenchymal destruction. Methods: Twenty six outpatients with COPD and eight healthy non-smokers were examined. Each subject underwent HRCT scanning, pulmonary function tests, cell counts, and measurements of neutrophil elastase, matrix metalloproteinase (MMP)-9 and tissue inhibitor of metalloproteinase (TIMP)-1 in induced sputum, as well as measurement of desmosine, a marker of elastin degradation in urine, plasma and sputum. Results: Patients with HRCT confirmed emphysema had a higher BODE index and lower IC/TLC ratio than subjects without HRCT confirmed emphysema and controls. Forced expiratory volume in 1 second (FEV1), FEV1/forced vital capacity ratio, and carbon monoxide transfer coefficient were lower, whereas the number of eosinophils, MMP-9, and the MMP-9/TIMP-1 ratio in sputum were higher in patients with emphysema. In COPD patients the number of sputum eosinophils was the biological variable that correlated positively with the HRCT score of emphysema (p = 0.04). Conclusions: These results suggest that COPD associated with HRCT confirmed emphysema is characterised by more severe lung function impairment, more intense airway inflammation and, possibly, more serious systemic dysfunction than COPD not associated with HRCT confirmed emphysema.
AbstractList The predominant emphysema phenotype is associated with more severe airflow limitation in patients with chronic obstructive pulmonary disease (COPD). A study was undertaken to investigate whether COPD patients, with or without emphysema quantitatively confirmed by high resolution computed tomography (HRCT), have different COPD severity as assessed by the BODE index (body mass index, airflow obstruction, dyspnoea, exercise performance) and inspiratory capacity to total lung capacity ratio (IC/TLC), and by different biological markers of lung parenchymal destruction. Twenty six outpatients with COPD and eight healthy non-smokers were examined. Each subject underwent HRCT scanning, pulmonary function tests, cell counts, and measurements of neutrophil elastase, matrix metalloproteinase (MMP)-9 and tissue inhibitor of metalloproteinase (TIMP)-1 in induced sputum, as well as measurement of desmosine, a marker of elastin degradation in urine, plasma and sputum. Patients with HRCT confirmed emphysema had a higher BODE index and lower IC/TLC ratio than subjects without HRCT confirmed emphysema and controls. Forced expiratory volume in 1 second (FEV(1)), FEV(1)/forced vital capacity ratio, and carbon monoxide transfer coefficient were lower, whereas the number of eosinophils, MMP-9, and the MMP-9/TIMP-1 ratio in sputum were higher in patients with emphysema. In COPD patients the number of sputum eosinophils was the biological variable that correlated positively with the HRCT score of emphysema (p = 0.04). These results suggest that COPD associated with HRCT confirmed emphysema is characterised by more severe lung function impairment, more intense airway inflammation and, possibly, more serious systemic dysfunction than COPD not associated with HRCT confirmed emphysema.
Background: The predominant emphysema phenotype is associated with more severe airflow limitation in patients with chronic obstructive pulmonary disease (COPD). A study was undertaken to investigate whether COPD patients, with or without emphysema quantitatively confirmed by high resolution computed tomography (HRCT), have different COPD severity as assessed by the BODE index (body mass index, airflow obstruction, dyspnoea, exercise performance) and inspiratory capacity to total lung capacity ratio (IC/TLC), and by different biological markers of lung parenchymal destruction. Methods: Twenty six outpatients with COPD and eight healthy non-smokers were examined. Each subject underwent HRCT scanning, pulmonary function tests, cell counts, and measurements of neutrophil elastase, matrix metalloproteinase (MMP)-9 and tissue inhibitor of metalloproteinase (TIMP)-1 in induced sputum, as well as measurement of desmosine, a marker of elastin degradation in urine, plasma and sputum. Results: Patients with HRCT confirmed emphysema had a higher BODE index and lower IC/TLC ratio than subjects without HRCT confirmed emphysema and controls. Forced expiratory volume in 1 second (FEV1), FEV1/forced vital capacity ratio, and carbon monoxide transfer coefficient were lower, whereas the number of eosinophils, MMP-9, and the MMP-9/TIMP-1 ratio in sputum were higher in patients with emphysema. In COPD patients the number of sputum eosinophils was the biological variable that correlated positively with the HRCT score of emphysema (p = 0.04). Conclusions: These results suggest that COPD associated with HRCT confirmed emphysema is characterised by more severe lung function impairment, more intense airway inflammation and, possibly, more serious systemic dysfunction than COPD not associated with HRCT confirmed emphysema.
The predominant emphysema phenotype is associated with more severe airflow limitation in patients with chronic obstructive pulmonary disease (COPD). A study was undertaken to investigate whether COPD patients, with or without emphysema quantitatively confirmed by high resolution computed tomography (HRCT), have different COPD severity as assessed by the BODE index (body mass index, airflow obstruction, dyspnoea, exercise performance) and inspiratory capacity to total lung capacity ratio (IC/TLC), and by different biological markers of lung parenchymal destruction.BACKGROUNDThe predominant emphysema phenotype is associated with more severe airflow limitation in patients with chronic obstructive pulmonary disease (COPD). A study was undertaken to investigate whether COPD patients, with or without emphysema quantitatively confirmed by high resolution computed tomography (HRCT), have different COPD severity as assessed by the BODE index (body mass index, airflow obstruction, dyspnoea, exercise performance) and inspiratory capacity to total lung capacity ratio (IC/TLC), and by different biological markers of lung parenchymal destruction.Twenty six outpatients with COPD and eight healthy non-smokers were examined. Each subject underwent HRCT scanning, pulmonary function tests, cell counts, and measurements of neutrophil elastase, matrix metalloproteinase (MMP)-9 and tissue inhibitor of metalloproteinase (TIMP)-1 in induced sputum, as well as measurement of desmosine, a marker of elastin degradation in urine, plasma and sputum.METHODSTwenty six outpatients with COPD and eight healthy non-smokers were examined. Each subject underwent HRCT scanning, pulmonary function tests, cell counts, and measurements of neutrophil elastase, matrix metalloproteinase (MMP)-9 and tissue inhibitor of metalloproteinase (TIMP)-1 in induced sputum, as well as measurement of desmosine, a marker of elastin degradation in urine, plasma and sputum.Patients with HRCT confirmed emphysema had a higher BODE index and lower IC/TLC ratio than subjects without HRCT confirmed emphysema and controls. Forced expiratory volume in 1 second (FEV(1)), FEV(1)/forced vital capacity ratio, and carbon monoxide transfer coefficient were lower, whereas the number of eosinophils, MMP-9, and the MMP-9/TIMP-1 ratio in sputum were higher in patients with emphysema. In COPD patients the number of sputum eosinophils was the biological variable that correlated positively with the HRCT score of emphysema (p = 0.04).RESULTSPatients with HRCT confirmed emphysema had a higher BODE index and lower IC/TLC ratio than subjects without HRCT confirmed emphysema and controls. Forced expiratory volume in 1 second (FEV(1)), FEV(1)/forced vital capacity ratio, and carbon monoxide transfer coefficient were lower, whereas the number of eosinophils, MMP-9, and the MMP-9/TIMP-1 ratio in sputum were higher in patients with emphysema. In COPD patients the number of sputum eosinophils was the biological variable that correlated positively with the HRCT score of emphysema (p = 0.04).These results suggest that COPD associated with HRCT confirmed emphysema is characterised by more severe lung function impairment, more intense airway inflammation and, possibly, more serious systemic dysfunction than COPD not associated with HRCT confirmed emphysema.CONCLUSIONSThese results suggest that COPD associated with HRCT confirmed emphysema is characterised by more severe lung function impairment, more intense airway inflammation and, possibly, more serious systemic dysfunction than COPD not associated with HRCT confirmed emphysema.
Author Fabbri, L M
Quintavalle, S
Zeni, E
Leprotti, S
Boschetto, P
Potena, A
Luisetti, M
Papi, A
Annovazzi, L
Palladini, G
Iadarola, P
De Rosa, E
Ballerin, L
Mapp, C E
AuthorAffiliation S Leprotti , Department of Surgery, Anesthesiology and Radiology, University of Ferrara, Ferrara, Italy
A Potena , L Ballerin , Section of Respiratory Physiopathology, University‐Hospital of Ferrara, Ferrara, Italy
G Palladini , Department of Internal Medicine, IRCCS San Matteo Hospital, University of Pavia, Pavia, Italy
L M Fabbri , Department of Medicine, Oncology and Radiology, Section of Respiratory Diseases, University of Modena & Reggio Emilia, Modena, Italy
L Annovazzi , P Iadarola , Department of Biochemistry, University of Pavia, Pavia, Italy
M Luisetti , Department of Respiratory Diseases, IRCCS San Matteo Hospital, University of Pavia, Pavia, Italy
P Boschetto , S Quintavalle , E Zeni , A Papi , E De Rosa , C E Mapp , Department of Experimental and Clinical Medicine, University of Ferrara, Ferrara, Italy
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Issue 12
Keywords Lung disease
Chronic
Association
Respiratory disease
Chronic disease
Biological marker
Bronchus disease
Cardiovascular disease
Obstructive pulmonary disease
Severe
Emphysema
Language English
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Correspondence to:
 Dr P Boschetto
 Dipartimento di Medicina Clinica e Sperimentale, Sezione di Igiene e Medicina del Lavoro, Via Fossato di Mortara 64/b, 44100 Ferrara, Italy; bsp@unife.it
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References_xml – reference: 17114369 - Thorax. 2006 Dec;61(12):1031-2
– reference: 7489808 - Eur Respir J. 1995 Aug;8(8):1398-420
– reference: 11943590 - Int J Biochem Cell Biol. 2002 Jun;34(6):594-604
– reference: 15591470 - Am J Respir Crit Care Med. 2005 Mar 15;171(6):591-7
– reference: 9759652 - Lab Invest. 1998 Sep;78(9):1077-87
– reference: 12200530 - Thorax. 2002 Sep;57(9):830-4
– reference: 12091180 - Am J Respir Crit Care Med. 2002 Jul 1;166(1):111-7
– reference: 3683459 - N Engl J Med. 1987 Nov 19;317(21):1309-14
– reference: 8499053 - Eur Respir J Suppl. 1993 Mar;16:41-52
– reference: 10420604 - J Chromatogr A. 1999 Jun 18;846(1-2):125-34
– reference: 8911175 - AJR Am J Roentgenol. 1996 Nov;167(5):1169-73
– reference: 15302769 - Chest. 2004 Aug;126(2 Suppl):96S-104S; discussion 159S-161S
– reference: 8499054 - Eur Respir J Suppl. 1993 Mar;16:5-40
– reference: 15802337 - Eur Respir J. 2005 Apr;25(4):640-6
– reference: 7697272 - Am J Respir Crit Care Med. 1995 Apr;151(4):952-9
– reference: 3168574 - Chest. 1988 Oct;94(4):782-7
– reference: 8074288 - Anal Biochem. 1994 May 1;218(2):325-9
– reference: 10885433 - Eur Respir J. 2000 Jun;15(6):1116-9
– reference: 14907713 - J Biol Chem. 1951 Nov;193(1):265-75
– reference: 10588615 - Am J Respir Crit Care Med. 1999 Dec;160(6):1968-75
– reference: 11287822 - Respiration. 2001;68(2):117-28
– reference: 11316667 - Am J Respir Crit Care Med. 2001 Apr;163(5):1256-76
– reference: 14999112 - N Engl J Med. 2004 Mar 4;350(10):1005-12
– reference: 9230755 - Am J Respir Crit Care Med. 1997 Jul;156(1):240-7
– reference: 15136381 - Chest. 2004 May;125(5):1714-8
– reference: 3525610 - J Clin Invest. 1986 Aug;78(2):482-93
– reference: 8912738 - Am J Respir Crit Care Med. 1996 Nov;154(5):1290-5
– reference: 14764080 - Eur J Clin Invest. 2004 Feb;34(2):156-64
– reference: 14312390 - Arch Environ Health. 1965 Jul;11:50-8
– reference: 9376127 - Am J Respir Cell Mol Biol. 1997 Oct;17(4):519-28
– reference: 14981697 - Electrophoresis. 2004 Feb;25(4-5):683-91
– reference: 14582923 - Eur Respir J. 2003 Oct;22(4):672-88
– reference: 12023833 - Biochem Soc Trans. 2002 Apr;30(2):98-102
– reference: 12662000 - Eur Respir J. 2003 Mar;21(3):450-4
– reference: 23527532 - COPD. 2013 Mar;10 Suppl 1:3-8
– reference: 9227714 - Thorax. 1997 Jun;52(6):502-6
– reference: 14522813 - Am J Respir Crit Care Med. 2003 Oct 1;168(7):818-900
– reference: 9847290 - Am J Respir Crit Care Med. 1998 Dec;158(6):1945-50
– reference: 11371392 - Am J Respir Crit Care Med. 2001 May;163(6):1304-9
– reference: 14563926 - Proc Natl Acad Sci U S A. 2003 Oct 28;100(22):12941-3
– reference: 15302709 - Chest. 2004 Aug;126(2):329-31
– reference: 11716178 - Eur Respir J. 2001 Oct;18(4):720-30
– reference: 3366931 - J Clin Pathol. 1988 Apr;41(4):435-40
– reference: 10885422 - Eur Respir J. 2000 Jun;15(6):1039-45
– reference: 3342669 - Chest. 1988 Mar;93(3):580-6
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Snippet Background: The predominant emphysema phenotype is associated with more severe airflow limitation in patients with chronic obstructive pulmonary disease...
The predominant emphysema phenotype is associated with more severe airflow limitation in patients with chronic obstructive pulmonary disease (COPD). A study...
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StartPage 1037
SubjectTerms Aged
airflow obstruction
arterial carbon dioxide tension
arterial oxygen tension
Biological and medical sciences
biological markers
Biomarkers - metabolism
BODE index
Body Mass Index
carbon monoxide transfer coefficient
Cell Count
Chronic Obstructive Pulmonary Disease
Chronic obstructive pulmonary disease, asthma
COPD
dyspnoea
Emphysema
exercise performance
Female
FEV1
Forced Expiratory Volume - physiology
forced expiratory volume in 1 second
forced vital capacity
FRC
functional residual capacity
FVC
high resolution computed tomography
HRCT
Humans
inspiratory capacity
Kco
Male
matrix metalloproteinase
Matrix Metalloproteinase 9 - metabolism
mean lung density
Medical sciences
MLD
MMP
neutrophil elastase
outcomes
Paco2
Pao2
Pneumology
Pulmonary Disease, Chronic Obstructive - etiology
Pulmonary Emphysema - complications
Pulmonary Emphysema - diagnostic imaging
Pulmonary Emphysema - physiopathology
residual volume
Sputum - cytology
TIMP
tissue inhibitor of metalloproteinase
Tissue Inhibitor of Metalloproteinase-1 - metabolism
TLC
Tomography
Tomography, X-Ray Computed
Total Lung Capacity
Urine
Vital Capacity - physiology
Title Association between markers of emphysema and more severe chronic obstructive pulmonary disease
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