TY - JOUR
T1 - Using bacterial biomarkers to identify early indicators of cystic fibrosis pulmonary exacerbation onset
AU - Rogers, Geraint B.
AU - Hoffman, Lucas R.
AU - Johnson, Matt W.
AU - Mayer-Hamblett, Nicole
AU - Schwarze, Jürgen
AU - Carroll, Mary P.
AU - Bruce, Kenneth D.
N1 - Funding Information:
1Molecular Microbiology Research Laboratory, Pharmaceutical Science Division, 150 Stamford Street, Franklin-Wilkins Building, King’s College London, London, SE1 9NH, UK 2Department of Pediatrics, University of Washington, Box 356320, HSB RR338, Seattle, WA 98105, USA 3Gastroenterology Surgical Department, St Mark’s Hospital, Harrow, Middlesex, UK 4Cystic Fibrosis Foundation, Therapeutics Development Network Coordinating Center, Children’s Hospital and Regional Medical Center, Seattle, WA, USA 5Child Life and Health and Centre for Inflammation Research, the University of Edinburgh, Queen’s Medical Research Institute, Edinburgh EH16 4TJ, UK 6Cystic Fibrosis Unit, Southampton University Hospital NHS Trust, Tremona Road, Southampton, SO16 6YD, UK †Author for correspondence: Tel.: +44 207 848 4620 [email protected]
PY - 2011/3
Y1 - 2011/3
N2 - Acute periods of pulmonary exacerbation are the single most important cause of morbidity in cystic fibrosis patients, and may be associated with a loss of lung function. Intervening prior to the onset of a substantially increased inflammatory response may limit the associated damage to the airways. While a number of biomarker assays based on inflammatory markers have been developed, providing useful and important measures of disease during these periods, such factors are typically only elevated once the process of exacerbation has been initiated. Identifying biomarkers that can predict the onset of pulmonary exacerbation at an early stage would provide an opportunity to intervene before the establishment of a substantial immune response, with major implications for the advancement of cystic fibrosis care. The precise triggers of pulmonary exacerbation remain to be determined; however, the majority of models relate to the activity of microbes present in the patient's lower airways of cystic fibrosis. Advances in diagnostic microbiology now allow for the examination of these complex systems at a level likely to identify factors on which biomarker assays can be based. In this article, we discuss key considerations in the design and testing of assays that could predict pulmonary exacerbations.
AB - Acute periods of pulmonary exacerbation are the single most important cause of morbidity in cystic fibrosis patients, and may be associated with a loss of lung function. Intervening prior to the onset of a substantially increased inflammatory response may limit the associated damage to the airways. While a number of biomarker assays based on inflammatory markers have been developed, providing useful and important measures of disease during these periods, such factors are typically only elevated once the process of exacerbation has been initiated. Identifying biomarkers that can predict the onset of pulmonary exacerbation at an early stage would provide an opportunity to intervene before the establishment of a substantial immune response, with major implications for the advancement of cystic fibrosis care. The precise triggers of pulmonary exacerbation remain to be determined; however, the majority of models relate to the activity of microbes present in the patient's lower airways of cystic fibrosis. Advances in diagnostic microbiology now allow for the examination of these complex systems at a level likely to identify factors on which biomarker assays can be based. In this article, we discuss key considerations in the design and testing of assays that could predict pulmonary exacerbations.
KW - biomarkers
KW - cystic fibrosis
KW - exhaled breath
KW - inflammation
KW - molecular diagnostics
KW - predictive biomarkers
KW - proteomics
KW - pulmonary exacerbation
KW - quantitative PCR
KW - sputum
KW - trace metals
UR - https://www.scopus.com/pages/publications/79952972412
U2 - 10.1586/erm.10.117
DO - 10.1586/erm.10.117
M3 - Review article
C2 - 21405970
AN - SCOPUS:79952972412
SN - 1473-7159
VL - 11
SP - 197
EP - 206
JO - Expert Review of Molecular Diagnostics
JF - Expert Review of Molecular Diagnostics
IS - 2
ER -