Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.

Progressive lung disease accounts for the majority of morbidity and mortality observed in cystic fibrosis (CF). Beyond secondhand smoke exposure and socio-economic status, the effect of specific environmental factors on CF lung function is largely unknown.Multivariate regression was used to assess c...

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Main Authors: Joseph M Collaco, John McGready, Deanna M Green, Kathleen M Naughton, Christopher P Watson, Timothy Shields, Scott C Bell, Claire E Wainwright, ACFBAL Study Group, Garry R Cutting
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3220679?pdf=render
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spelling doaj-e5cf7dc2d16e400786deaf276a82aa0e2020-11-25T02:32:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01611e2778410.1371/journal.pone.0027784Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.Joseph M CollacoJohn McGreadyDeanna M GreenKathleen M NaughtonChristopher P WatsonTimothy ShieldsScott C BellClaire E WainwrightACFBAL Study GroupGarry R CuttingProgressive lung disease accounts for the majority of morbidity and mortality observed in cystic fibrosis (CF). Beyond secondhand smoke exposure and socio-economic status, the effect of specific environmental factors on CF lung function is largely unknown.Multivariate regression was used to assess correlation between specific environmental factors, the presence of pulmonary pathogens, and variation in lung function using subjects enrolled in the U.S. CF Twin and Sibling Study (CFTSS: n = 1378). Significant associations were tested for replication in the U.S. CF Foundation Patient Registry (CFF: n = 16439), the Australian CF Data Registry (ACFDR: n = 1801), and prospectively ascertained subjects from Australia/New Zealand (ACFBAL: n = 167).In CFTSS subjects, the presence of Pseudomonas aeruginosa (OR = 1.06 per °F; p<0.001) was associated with warmer annual ambient temperatures. This finding was independently replicated in the CFF (1.02; p<0.001), ACFDR (1.05; p = 0.002), and ACFBAL (1.09; p = 0.003) subjects. Warmer temperatures (-0.34 points per °F; p = 0.005) and public insurance (-6.43 points; p<0.001) were associated with lower lung function in the CFTSS subjects. These findings were replicated in the CFF subjects (temperature: -0.31; p<0.001; insurance: -9.11; p<0.001) and similar in the ACFDR subjects (temperature: -0.23; p = 0.057). The association between temperature and lung function was minimally influenced by P. aeruginosa. Similarly, the association between temperature and P. aeruginosa was largely independent of lung function.Ambient temperature is associated with prevalence of P. aeruginosa and lung function in four independent samples of CF patients from two continents.http://europepmc.org/articles/PMC3220679?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Joseph M Collaco
John McGready
Deanna M Green
Kathleen M Naughton
Christopher P Watson
Timothy Shields
Scott C Bell
Claire E Wainwright
ACFBAL Study Group
Garry R Cutting
spellingShingle Joseph M Collaco
John McGready
Deanna M Green
Kathleen M Naughton
Christopher P Watson
Timothy Shields
Scott C Bell
Claire E Wainwright
ACFBAL Study Group
Garry R Cutting
Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.
PLoS ONE
author_facet Joseph M Collaco
John McGready
Deanna M Green
Kathleen M Naughton
Christopher P Watson
Timothy Shields
Scott C Bell
Claire E Wainwright
ACFBAL Study Group
Garry R Cutting
author_sort Joseph M Collaco
title Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.
title_short Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.
title_full Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.
title_fullStr Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.
title_full_unstemmed Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.
title_sort effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Progressive lung disease accounts for the majority of morbidity and mortality observed in cystic fibrosis (CF). Beyond secondhand smoke exposure and socio-economic status, the effect of specific environmental factors on CF lung function is largely unknown.Multivariate regression was used to assess correlation between specific environmental factors, the presence of pulmonary pathogens, and variation in lung function using subjects enrolled in the U.S. CF Twin and Sibling Study (CFTSS: n = 1378). Significant associations were tested for replication in the U.S. CF Foundation Patient Registry (CFF: n = 16439), the Australian CF Data Registry (ACFDR: n = 1801), and prospectively ascertained subjects from Australia/New Zealand (ACFBAL: n = 167).In CFTSS subjects, the presence of Pseudomonas aeruginosa (OR = 1.06 per °F; p<0.001) was associated with warmer annual ambient temperatures. This finding was independently replicated in the CFF (1.02; p<0.001), ACFDR (1.05; p = 0.002), and ACFBAL (1.09; p = 0.003) subjects. Warmer temperatures (-0.34 points per °F; p = 0.005) and public insurance (-6.43 points; p<0.001) were associated with lower lung function in the CFTSS subjects. These findings were replicated in the CFF subjects (temperature: -0.31; p<0.001; insurance: -9.11; p<0.001) and similar in the ACFDR subjects (temperature: -0.23; p = 0.057). The association between temperature and lung function was minimally influenced by P. aeruginosa. Similarly, the association between temperature and P. aeruginosa was largely independent of lung function.Ambient temperature is associated with prevalence of P. aeruginosa and lung function in four independent samples of CF patients from two continents.
url http://europepmc.org/articles/PMC3220679?pdf=render
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