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Predictive modeling of COPD exacerbation rates using baseline risk factors
BACKGROUND: Demographic and disease characteristics have been associated with the risk of chronic obstructive pulmonary disease (COPD) exacerbations. Using previously collected multinational clinical trial data, we developed models that use baseline risk factors to predict an individual’s rate of mo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340368/ https://www.ncbi.nlm.nih.gov/pubmed/35815359 http://dx.doi.org/10.1177/17534666221107314 |
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author | Singh, Dave Hurst, John R. Martinez, Fernando J. Rabe, Klaus F. Bafadhel, Mona Jenkins, Martin Salazar, Domingo Dorinsky, Paul Darken, Patrick |
author_facet | Singh, Dave Hurst, John R. Martinez, Fernando J. Rabe, Klaus F. Bafadhel, Mona Jenkins, Martin Salazar, Domingo Dorinsky, Paul Darken, Patrick |
author_sort | Singh, Dave |
collection | PubMed |
description | BACKGROUND: Demographic and disease characteristics have been associated with the risk of chronic obstructive pulmonary disease (COPD) exacerbations. Using previously collected multinational clinical trial data, we developed models that use baseline risk factors to predict an individual’s rate of moderate/severe exacerbations in the next year on various pharmacological treatments for COPD. METHODS: Exacerbation data from 20,054 patients in the ETHOS, KRONOS, TELOS, SOPHOS, and PINNACLE-1, PINNACLE-2, and PINNACLE-4 studies were pooled. Machine learning was used to identify predictors of moderate/severe exacerbation rates. Important factors were selected for generalized linear modeling, further informed by backward variable selection. An independent test set was held back for validation. RESULTS: Prior exacerbations, eosinophil count, forced expiratory volume in 1 s percent predicted, prior maintenance treatments, reliever medication use, sex, COPD Assessment Test score, smoking status, and region were significant predictors of exacerbation risk, with response to inhaled corticosteroids (ICSs) increasing with higher eosinophil counts, more prior exacerbations, or additional prior treatments. Model fit was similar in the training and test set. Prediction metrics were ~10% better in the full model than in a simplified model based only on eosinophil count, prior exacerbations, and ICS use. CONCLUSION: These models predicting rates of moderate/severe exacerbations can be applied to a broad range of patients with COPD in terms of airway obstruction, eosinophil counts, exacerbation history, symptoms, and treatment history. Understanding the relative and absolute risks related to these factors may be useful for clinicians in evaluating the benefit: risk ratio of various treatment decisions for individual patients. Clinical trials registered with www.clinicaltrials.gov (NCT02465567, NCT02497001, NCT02766608, NCT02727660, NCT01854645, NCT01854658, NCT02343458, NCT03262012, NCT02536508, and NCT01970878) |
format | Online Article Text |
id | pubmed-9340368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-93403682022-08-02 Predictive modeling of COPD exacerbation rates using baseline risk factors Singh, Dave Hurst, John R. Martinez, Fernando J. Rabe, Klaus F. Bafadhel, Mona Jenkins, Martin Salazar, Domingo Dorinsky, Paul Darken, Patrick Ther Adv Respir Dis Original Research BACKGROUND: Demographic and disease characteristics have been associated with the risk of chronic obstructive pulmonary disease (COPD) exacerbations. Using previously collected multinational clinical trial data, we developed models that use baseline risk factors to predict an individual’s rate of moderate/severe exacerbations in the next year on various pharmacological treatments for COPD. METHODS: Exacerbation data from 20,054 patients in the ETHOS, KRONOS, TELOS, SOPHOS, and PINNACLE-1, PINNACLE-2, and PINNACLE-4 studies were pooled. Machine learning was used to identify predictors of moderate/severe exacerbation rates. Important factors were selected for generalized linear modeling, further informed by backward variable selection. An independent test set was held back for validation. RESULTS: Prior exacerbations, eosinophil count, forced expiratory volume in 1 s percent predicted, prior maintenance treatments, reliever medication use, sex, COPD Assessment Test score, smoking status, and region were significant predictors of exacerbation risk, with response to inhaled corticosteroids (ICSs) increasing with higher eosinophil counts, more prior exacerbations, or additional prior treatments. Model fit was similar in the training and test set. Prediction metrics were ~10% better in the full model than in a simplified model based only on eosinophil count, prior exacerbations, and ICS use. CONCLUSION: These models predicting rates of moderate/severe exacerbations can be applied to a broad range of patients with COPD in terms of airway obstruction, eosinophil counts, exacerbation history, symptoms, and treatment history. Understanding the relative and absolute risks related to these factors may be useful for clinicians in evaluating the benefit: risk ratio of various treatment decisions for individual patients. Clinical trials registered with www.clinicaltrials.gov (NCT02465567, NCT02497001, NCT02766608, NCT02727660, NCT01854645, NCT01854658, NCT02343458, NCT03262012, NCT02536508, and NCT01970878) SAGE Publications 2022-07-09 /pmc/articles/PMC9340368/ /pubmed/35815359 http://dx.doi.org/10.1177/17534666221107314 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Singh, Dave Hurst, John R. Martinez, Fernando J. Rabe, Klaus F. Bafadhel, Mona Jenkins, Martin Salazar, Domingo Dorinsky, Paul Darken, Patrick Predictive modeling of COPD exacerbation rates using baseline risk factors |
title | Predictive modeling of COPD exacerbation rates using baseline risk
factors |
title_full | Predictive modeling of COPD exacerbation rates using baseline risk
factors |
title_fullStr | Predictive modeling of COPD exacerbation rates using baseline risk
factors |
title_full_unstemmed | Predictive modeling of COPD exacerbation rates using baseline risk
factors |
title_short | Predictive modeling of COPD exacerbation rates using baseline risk
factors |
title_sort | predictive modeling of copd exacerbation rates using baseline risk
factors |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340368/ https://www.ncbi.nlm.nih.gov/pubmed/35815359 http://dx.doi.org/10.1177/17534666221107314 |
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