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Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study
BACKGROUND: Acute pulmonary exacerbations are associated with progressive lung function decline and increased mortality in cystic fibrosis (CF). The role of pulmonary vascular disease in pulmonary exacerbations is unknown. We investigated the association between pulmonary artery enlargement (PA:A>...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5672808/ https://www.ncbi.nlm.nih.gov/pubmed/27298019 http://dx.doi.org/10.1016/S2213-2600(16)30105-9 |
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author | Wells, J. Michael Farris, Roopan F. Gosdin, Taylor A. Dransfield, Mark T. Wood, Michelle E. Bell, Scott C. Rowe, Steven M. |
author_facet | Wells, J. Michael Farris, Roopan F. Gosdin, Taylor A. Dransfield, Mark T. Wood, Michelle E. Bell, Scott C. Rowe, Steven M. |
author_sort | Wells, J. Michael |
collection | PubMed |
description | BACKGROUND: Acute pulmonary exacerbations are associated with progressive lung function decline and increased mortality in cystic fibrosis (CF). The role of pulmonary vascular disease in pulmonary exacerbations is unknown. We investigated the association between pulmonary artery enlargement (PA:A>1), a marker of pulmonary vascular disease, and exacerbations. METHODS: We analyzed clinical, computed tomography (CT), and prospective exacerbation data in a derivation cohort of 74 adult CF patients, measuring the PA:A at the level of the PA bifurcation. We then replicated our findings in a validation cohort of 190 adult CF patients. Patients were separated into groups based on the presence or absence of a PA:A>1 and were followed for 1-year in the derivation cohort and 2-years in the validation cohort. The primary endpoint was developing ≥1 acute pulmonary exacerbation during follow-up. Linear and logistic regression models were used to determine associations between clinical factors, the PA:A ratio, and pulmonary exacerbations. We used Cox regression to determine time to first exacerbation in the validation cohort. FINDINGS: We found that PA:A>1 was present in n=37/74 (50%) of the derivation and n=89/190 (47%) of the validation cohort. In the derivation cohort, n=50/74 (68%) had ≥1 exacerbation at 1 year and n=133/190 (70%) in the validation cohort had ≥1 exacerbation after 2 years. PA:A>1 was associated with younger age in both cohorts and with elevated sweat chloride (100.5±10.9 versus 90.4±19.9mmol/L, difference between groups 10.1mmol/L [95%CI 2.5–17.7], P=0.017) in the derivation group. PA:A>1 was associated with exacerbations in the derivation (OR 3.49, 95%CI 1.18–10.3, P=0.023) and validation (OR 2.41, 95%CI 1.06–5.52, P=0.037) cohorts when adjusted for confounders. Time to first exacerbation was shorter in PA:A>1 versus PA:A<1 [HR 1.66 (95%CI 1.18–2.34), P=0.004] in unadjusted analysis, but not when adjusted for sex, BMI, prior exacerbation, positive Pseudomonas status, and FEV1/FVC [HR 1.14 (95%CI 0.80–1.62), P=0.82]). INTERPRETATION: PA enlargement is prevalent in adult CF patients and is associated with acute pulmonary exacerbation risk in two well-characterized cohorts. PA:A may be a predictive marker in CF. |
format | Online Article Text |
id | pubmed-5672808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-56728082017-11-06 Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study Wells, J. Michael Farris, Roopan F. Gosdin, Taylor A. Dransfield, Mark T. Wood, Michelle E. Bell, Scott C. Rowe, Steven M. Lancet Respir Med Article BACKGROUND: Acute pulmonary exacerbations are associated with progressive lung function decline and increased mortality in cystic fibrosis (CF). The role of pulmonary vascular disease in pulmonary exacerbations is unknown. We investigated the association between pulmonary artery enlargement (PA:A>1), a marker of pulmonary vascular disease, and exacerbations. METHODS: We analyzed clinical, computed tomography (CT), and prospective exacerbation data in a derivation cohort of 74 adult CF patients, measuring the PA:A at the level of the PA bifurcation. We then replicated our findings in a validation cohort of 190 adult CF patients. Patients were separated into groups based on the presence or absence of a PA:A>1 and were followed for 1-year in the derivation cohort and 2-years in the validation cohort. The primary endpoint was developing ≥1 acute pulmonary exacerbation during follow-up. Linear and logistic regression models were used to determine associations between clinical factors, the PA:A ratio, and pulmonary exacerbations. We used Cox regression to determine time to first exacerbation in the validation cohort. FINDINGS: We found that PA:A>1 was present in n=37/74 (50%) of the derivation and n=89/190 (47%) of the validation cohort. In the derivation cohort, n=50/74 (68%) had ≥1 exacerbation at 1 year and n=133/190 (70%) in the validation cohort had ≥1 exacerbation after 2 years. PA:A>1 was associated with younger age in both cohorts and with elevated sweat chloride (100.5±10.9 versus 90.4±19.9mmol/L, difference between groups 10.1mmol/L [95%CI 2.5–17.7], P=0.017) in the derivation group. PA:A>1 was associated with exacerbations in the derivation (OR 3.49, 95%CI 1.18–10.3, P=0.023) and validation (OR 2.41, 95%CI 1.06–5.52, P=0.037) cohorts when adjusted for confounders. Time to first exacerbation was shorter in PA:A>1 versus PA:A<1 [HR 1.66 (95%CI 1.18–2.34), P=0.004] in unadjusted analysis, but not when adjusted for sex, BMI, prior exacerbation, positive Pseudomonas status, and FEV1/FVC [HR 1.14 (95%CI 0.80–1.62), P=0.82]). INTERPRETATION: PA enlargement is prevalent in adult CF patients and is associated with acute pulmonary exacerbation risk in two well-characterized cohorts. PA:A may be a predictive marker in CF. 2016-06-10 2016-08 /pmc/articles/PMC5672808/ /pubmed/27298019 http://dx.doi.org/10.1016/S2213-2600(16)30105-9 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This manuscript version is made available under the CC BY-NC-ND 4.0 license. |
spellingShingle | Article Wells, J. Michael Farris, Roopan F. Gosdin, Taylor A. Dransfield, Mark T. Wood, Michelle E. Bell, Scott C. Rowe, Steven M. Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study |
title | Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study |
title_full | Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study |
title_fullStr | Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study |
title_full_unstemmed | Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study |
title_short | Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study |
title_sort | pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5672808/ https://www.ncbi.nlm.nih.gov/pubmed/27298019 http://dx.doi.org/10.1016/S2213-2600(16)30105-9 |
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