Effect of Temperature on Cystic Fibrosis Lung Disease and Infections: A Replicated Cohort Study
Joseph M Collaco,
John McGready,
Deanna M Green,
Kathleen M Naughton,
Christopher P Watson,
Timothy Shields,
Scott C Bell,
Claire E Wainwright and
Garry R. Cutting 3 for the ACFBAL Study Group
PLOS ONE, 2011, vol. 6, issue 11, 1-7
Abstract:
Background: 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. Methods: 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). Results: In CFTSS subjects, the presence of Pseudomonas aeruginosa (OR = 1.06 per °F; p
Date: 2011
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Persistent link: https://EconPapers.repec.org/RePEc:plo:pone00:0027784
DOI: 10.1371/journal.pone.0027784
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