TY - JOUR
T1 - Pulmonary biomarkers in chronic obstructive pulmonary disease
AU - Barnes, Peter J.
AU - Chowdhury, Badrul
AU - Kharitonov, Sergei A.
AU - Magnussen, Helgo
AU - Page, Clive P.
AU - Postma, Dirkje
AU - Saetta, Marina
N1 - Review J
PY - 2006/7/1
Y1 - 2006/7/1
N2 - There has been increasing interest in using pulmonary biomarkers to understand and monitor the inflammation in the respiratory tract of patients with chronic obstructive pulmonary disease (COPD). In this Pulmonary Perspective we discuss the merits of the various approaches by reviewing the current literature on pulmonary biomarkers in COPD and underscore the need for more systematic studies in the future. Bronchial biopsies and bronchoalveolar lavage provide valuable information about inflammatory cells and mediators, but are invasive, so that repeated measurements have to be very limited in assessing any interventions. Induced sputum has provided considerable information about the inflammatory process, including mediators and proteinases in COPD, but selectively samples proximal airways and may not closely reflect distal inflammatory processes. Exhaled gases and breath condensate are noninvasive procedures, so repeated measurements are possible, but for some assays the variability is relatively high. There is relatively little information about how any of these biomarkers relate to other clinical outcomes, such as progression of the disease, severity of disease, clinical subtypes, or response to therapy. More information is also needed about the variability in these measurements. In the future, pulmonary biomarkers may be useful in predicting disease progression, indicating disease instability, and in predicting response to current therapies and novel therapies, many of which are now in development.
AB - There has been increasing interest in using pulmonary biomarkers to understand and monitor the inflammation in the respiratory tract of patients with chronic obstructive pulmonary disease (COPD). In this Pulmonary Perspective we discuss the merits of the various approaches by reviewing the current literature on pulmonary biomarkers in COPD and underscore the need for more systematic studies in the future. Bronchial biopsies and bronchoalveolar lavage provide valuable information about inflammatory cells and mediators, but are invasive, so that repeated measurements have to be very limited in assessing any interventions. Induced sputum has provided considerable information about the inflammatory process, including mediators and proteinases in COPD, but selectively samples proximal airways and may not closely reflect distal inflammatory processes. Exhaled gases and breath condensate are noninvasive procedures, so repeated measurements are possible, but for some assays the variability is relatively high. There is relatively little information about how any of these biomarkers relate to other clinical outcomes, such as progression of the disease, severity of disease, clinical subtypes, or response to therapy. More information is also needed about the variability in these measurements. In the future, pulmonary biomarkers may be useful in predicting disease progression, indicating disease instability, and in predicting response to current therapies and novel therapies, many of which are now in development.
KW - bronchial biopsy
KW - bronchoalveolar lavage
KW - exhaled breath
KW - condensate
KW - exhaled nitric oxide
KW - induced sputum
KW - EXHALED BREATH CONDENSATE
KW - BRONCHOALVEOLAR LAVAGE FLUID
KW - RANDOMIZED CONTROLLED-TRIAL
KW - NITRIC-OXIDE MEASUREMENTS
KW - AIR-FLOW OBSTRUCTION
KW - SPUTUM INFLAMMATORY MARKERS
KW - SHORT-TERM RESPONSE
KW - CHRONIC-BRONCHITIS
KW - OXIDATIVE STRESS
KW - SMOKING-CESSATION
U2 - 10.1164/rccm.200510-1659PP
DO - 10.1164/rccm.200510-1659PP
M3 - Article
SN - 1073-449X
VL - 174
SP - 6
EP - 14
JO - American Journal of Respiratory and Critical Care Medicine
JF - American Journal of Respiratory and Critical Care Medicine
IS - 1
ER -