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Chlorinated Pool Attendance, Atopy, and the Risk of Asthma during Childhood

The pool chlorine hypothesis postulates that the rise in childhood asthma in the developed world could result at least partly from the increasing exposure of children to toxic gases and aerosols contaminating the air of indoor chlorinated pools. To further assess this hypothesis, we explored the rel...

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Autores principales: Bernard, Alfred, Carbonnelle, Sylviane, de Burbure, Claire, Michel, Olivier, Nickmilder, Marc
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626429/
https://www.ncbi.nlm.nih.gov/pubmed/17035144
http://dx.doi.org/10.1289/ehp.8461
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author Bernard, Alfred
Carbonnelle, Sylviane
de Burbure, Claire
Michel, Olivier
Nickmilder, Marc
author_facet Bernard, Alfred
Carbonnelle, Sylviane
de Burbure, Claire
Michel, Olivier
Nickmilder, Marc
author_sort Bernard, Alfred
collection PubMed
description The pool chlorine hypothesis postulates that the rise in childhood asthma in the developed world could result at least partly from the increasing exposure of children to toxic gases and aerosols contaminating the air of indoor chlorinated pools. To further assess this hypothesis, we explored the relationships between childhood asthma, atopy, and cumulated pool attendance (CPA). We studied 341 schoolchildren 10–13 years of age who attended at a variable rate the same public pool in Brussels (trichloramine in air, 0.3–0.5 mg/m(3)). Examination of the children included a questionnaire, an exercise-induced bronchoconstriction (EIB) test, and the measurement of exhaled nitric oxide (eNO) and total and aeroallergen-specific serum IgE. CPA by children (range, 0–1,818 hr) emerged among the most consistent predictors of asthma (doctor diagnosed or screened with the EIB test) and of elevated eNO, ranking immediately after atopy and family history of asthma or hay fever. Although the risk of elevated eNO increased with CPA [odds ratio (OR) = 1.30; 95% confidence interval (CI), 1.10–1.43] independently of total or specific serum IgE, the probability of developing asthma increased with CPA only in children with serum IgE > 100 kIU/L (OR for each 100-hr increase in CPA = 1.79; 95% CI, 1.07–2.72). All these effects were dose related and most strongly linked to pool attendance before 6–7 years of age. Use of indoor chlorinated pools especially by young children interacts with atopic status to promote the development of childhood asthma. These findings further support the hypothesis implicating pool chlorine in the rise of childhood asthma in industrialized countries.
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spelling pubmed-16264292006-11-08 Chlorinated Pool Attendance, Atopy, and the Risk of Asthma during Childhood Bernard, Alfred Carbonnelle, Sylviane de Burbure, Claire Michel, Olivier Nickmilder, Marc Environ Health Perspect Research The pool chlorine hypothesis postulates that the rise in childhood asthma in the developed world could result at least partly from the increasing exposure of children to toxic gases and aerosols contaminating the air of indoor chlorinated pools. To further assess this hypothesis, we explored the relationships between childhood asthma, atopy, and cumulated pool attendance (CPA). We studied 341 schoolchildren 10–13 years of age who attended at a variable rate the same public pool in Brussels (trichloramine in air, 0.3–0.5 mg/m(3)). Examination of the children included a questionnaire, an exercise-induced bronchoconstriction (EIB) test, and the measurement of exhaled nitric oxide (eNO) and total and aeroallergen-specific serum IgE. CPA by children (range, 0–1,818 hr) emerged among the most consistent predictors of asthma (doctor diagnosed or screened with the EIB test) and of elevated eNO, ranking immediately after atopy and family history of asthma or hay fever. Although the risk of elevated eNO increased with CPA [odds ratio (OR) = 1.30; 95% confidence interval (CI), 1.10–1.43] independently of total or specific serum IgE, the probability of developing asthma increased with CPA only in children with serum IgE > 100 kIU/L (OR for each 100-hr increase in CPA = 1.79; 95% CI, 1.07–2.72). All these effects were dose related and most strongly linked to pool attendance before 6–7 years of age. Use of indoor chlorinated pools especially by young children interacts with atopic status to promote the development of childhood asthma. These findings further support the hypothesis implicating pool chlorine in the rise of childhood asthma in industrialized countries. National Institute of Environmental Health Sciences 2006-10 2006-06-08 /pmc/articles/PMC1626429/ /pubmed/17035144 http://dx.doi.org/10.1289/ehp.8461 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Bernard, Alfred
Carbonnelle, Sylviane
de Burbure, Claire
Michel, Olivier
Nickmilder, Marc
Chlorinated Pool Attendance, Atopy, and the Risk of Asthma during Childhood
title Chlorinated Pool Attendance, Atopy, and the Risk of Asthma during Childhood
title_full Chlorinated Pool Attendance, Atopy, and the Risk of Asthma during Childhood
title_fullStr Chlorinated Pool Attendance, Atopy, and the Risk of Asthma during Childhood
title_full_unstemmed Chlorinated Pool Attendance, Atopy, and the Risk of Asthma during Childhood
title_short Chlorinated Pool Attendance, Atopy, and the Risk of Asthma during Childhood
title_sort chlorinated pool attendance, atopy, and the risk of asthma during childhood
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626429/
https://www.ncbi.nlm.nih.gov/pubmed/17035144
http://dx.doi.org/10.1289/ehp.8461
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