Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pone.0143793
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dc.title | Prediction of long-term benefits of inhaled steroids by phenotypic markers in moderateto-severe COPD: A randomized controlled trial | |
dc.contributor.author | Snoeck-Stroband J.B. | |
dc.contributor.author | Lapperre T.S. | |
dc.contributor.author | Sterk P.J. | |
dc.contributor.author | Hiemstra P.S. | |
dc.contributor.author | Thiadens H.A. | |
dc.contributor.author | Boezen H.M. | |
dc.contributor.author | Ten Hacken N.H.T. | |
dc.contributor.author | Kerstjens H.A.M. | |
dc.contributor.author | Postma D.S. | |
dc.contributor.author | Timens W. | |
dc.contributor.author | Sont J.K. | |
dc.date.accessioned | 2020-03-19T07:50:22Z | |
dc.date.available | 2020-03-19T07:50:22Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Snoeck-Stroband J.B., Lapperre T.S., Sterk P.J., Hiemstra P.S., Thiadens H.A., Boezen H.M., Ten Hacken N.H.T., Kerstjens H.A.M., Postma D.S., Timens W., Sont J.K. (2015). Prediction of long-term benefits of inhaled steroids by phenotypic markers in moderateto-severe COPD: A randomized controlled trial. PLoS ONE 10 (12) : 143793. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0143793 | |
dc.identifier.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/165757 | |
dc.description.abstract | Background The decline in lung function can be reduced by long-term inhaled corticosteroid (ICS) treatment in subsets of patients with chronic obstructive pulmonary disease (COPD).We aimed to identify which clinical, physiological and non-invasive inflammatory characteristics predict the benefits of ICS on lung function decline in COPD. Methods Analysis was performed in 50 steroid-naive compliant patients with moderate to severe COPD (postbronchodilator forced expiratory volume in one second (FEV1), 30-80% of predicted, compatible with GOLD stages II-III), age 45-75 years, >10 packyears smoking and without asthma. Patients were treated with fluticasone propionate (500 ?g bid) or placebo for 2.5 years. Postbronchodilator FEV1, dyspnea and health status were measured every 3 months; lung volumes, airway hyperresponsiveness (PC20), and induced sputum at 0, 6 and 30 months. A linear mixed effect model was used for analysis of this hypothesis generating study. Results Significant predictors of attenuated FEV1-decline by fluticasone treatment compared to placebo were: fewer packyears smoking, preserved diffusion capacity, limited hyperinflation and lower inflammatory cell counts in induced sputum (p<0.04). Conclusions Long-term benefits of ICS on lung function decline in patients with moderate-to-severe COPD are most pronounced in patients with fewer packyears, and less severe emphysema and inflammation. These data generate novel hypotheses on phenotype-driven therapy in COPD. Copyright: © 2015 Snoeck-Stroband et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | |
dc.publisher | Public Library of Science | |
dc.source | Unpaywall 20200320 | |
dc.subject | fluticasone propionate | |
dc.subject | placebo | |
dc.subject | bronchodilating agent | |
dc.subject | corticosteroid | |
dc.subject | fluticasone | |
dc.subject | adult | |
dc.subject | aged | |
dc.subject | Article | |
dc.subject | cell count | |
dc.subject | chronic obstructive lung disease | |
dc.subject | clinical effectiveness | |
dc.subject | controlled study | |
dc.subject | disease severity | |
dc.subject | double blind procedure | |
dc.subject | drug efficacy | |
dc.subject | dyspnea | |
dc.subject | female | |
dc.subject | forced expiratory volume | |
dc.subject | health status | |
dc.subject | human | |
dc.subject | inflammatory cell | |
dc.subject | lung diffusion capacity | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | multicenter study | |
dc.subject | phenotype | |
dc.subject | prediction | |
dc.subject | randomized controlled trial | |
dc.subject | smoking | |
dc.subject | treatment duration | |
dc.subject | treatment outcome | |
dc.subject | clinical trial | |
dc.subject | drug administration | |
dc.subject | inhalational drug administration | |
dc.subject | lung | |
dc.subject | middle aged | |
dc.subject | pathology | |
dc.subject | pathophysiology | |
dc.subject | physiology | |
dc.subject | placebo effect | |
dc.subject | Pulmonary Disease, Chronic Obstructive | |
dc.subject | severity of illness index | |
dc.subject | spirometry | |
dc.subject | sputum | |
dc.subject | Administration, Inhalation | |
dc.subject | Adrenal Cortex Hormones | |
dc.subject | Aged | |
dc.subject | Bronchodilator Agents | |
dc.subject | Drug Administration Schedule | |
dc.subject | Female | |
dc.subject | Fluticasone | |
dc.subject | Forced Expiratory Volume | |
dc.subject | Humans | |
dc.subject | Lung | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Phenotype | |
dc.subject | Placebo Effect | |
dc.subject | Pulmonary Disease, Chronic Obstructive | |
dc.subject | Severity of Illness Index | |
dc.subject | Spirometry | |
dc.subject | Sputum | |
dc.subject | Treatment Outcome | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.description.doi | 10.1371/journal.pone.0143793 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 10 | |
dc.description.issue | 12 | |
dc.description.page | 143793 | |
Appears in Collections: | Elements Staff Publications |
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