English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/27630
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE
Exportar a otros formatos:

Title

Short-Term Changes in Respiratory Biomarkers after Swimming in a Chlorinated Pool

AuthorsFont-Ribera, Laia; Kogevinas, Manolis; Zock, Jan-Paul; Gómez, Federico P.; Barreiro, Esther; Nieuwenhuijsen, Mark J.; Fernández, Pilar ; Lourencetti, Carolina; Pérez-Olabarría, Maitane; Bustamante, Mariona; Marcos, Ricard; Grimalt, Joan O. ; Villanueva, Cristina M.
KeywordsBiomarkers
Clara cell secretory protein
Disinfection by-products
Exhaled breath condensate
Fractional exhaled nitric oxide
Respiratory health
Swimming
Swimming pools
Trihalomethanes
Issue Date12-Sep-2010
PublisherNational Institute of Environmental Health Sciences (U.S.)
National Institutes of Health (U.S.). PubMed Central
Department of Health and Human Services (U.S.)
CitationEnvironmental Health Perspectives (EHP): (2010)
Abstract[BACKGROUND]: Swimming in chlorinated pools involves exposure to disinfection by-products (DBPs) and has been associated with impaired respiratory health.
[OBJECTIVES]: We evaluated short-term changes in several respiratory biomarkers to explore mechanisms of potential lung damage related to swimming pool exposure.
[METHODS]: We measured lung function and biomarkers of airway inflammation (fractional exhaled nitric oxide –FeNO- and 8 cytokines and 1 growth factor (VEGF) in exhaled breath condensate), oxidative stress (8-isoprostane in exhaled breath condensate), and lung permeability (surfactant protein D -SPD- and the Clara cell secretory protein -CC16- in serum) in 48 healthy non-smoking adults before and after swimming for 40 min in a chlorinated indoor swimming pool. We measured trihalomethanes in exhaled breath as a marker of individual exposure to DBPs. Energy expenditure during swimming, atopy and CC16 genotype (rs3741240) was also determined.
[RESULTS]: Median serum CC16 levels increased from 6.01 to 6.21 μg/L (average increase 3.3%, paired Wilcoxon test p = 0.03), regardless of atopic status and CC16 genotype. This increase was explained both by energy expenditure and different markers of DBP exposure in multivariate models. FeNO was unchanged overall but tended to decrease among atopics. We found no significant changes in lung function, SP-D, 8-isoprostane, 8 cytokines and VEGF.
[CONCLUSIONS]: A slight increase in serum CC16, a marker of lung epithelium permeability, was detected in healthy adults after swimming in an indoor chlorinated pool. Exercise and DBP exposure explained this association, without involving inflammatory mechanisms. Further research is needed to confirm the results, establish the clinical relevance of short-term serum CC16 changes, and evaluate the long-term health impacts.
Description36 páginas, 3 figuras, 5 tablas.
Publisher version (URL)http://dx.doi.org/10.1289/ehp.1001961
URIhttp://hdl.handle.net/10261/27630
DOIhttp://dx.doi.org/10.1289/ehp.1001961
ISSN0091-6765
Appears in Collections:(IDAEA) Artículos
Files in This Item:
File Description SizeFormat 
ehp.1001961.pdf252,43 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.