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Early-life exposure to PM(2.5) and risk of acute asthma clinical encounters among children in Massachusetts: a case-crossover analysis

BACKGROUND: Associations between ambient particulate matter < 2.5 μm (PM(2.5)) and asthma morbidity have been suggested in previous epidemiologic studies but results are inconsistent for areas with lower PM(2.5) levels. We estimated the associations between early-life short-term PM(2.5) exposure...

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Detalles Bibliográficos
Autores principales: Khalili, Roxana, Bartell, Scott M., Hu, Xuefei, Liu, Yang, Chang, Howard H., Belanoff, Candice, Strickland, Matthew J., Vieira, Verónica M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822480/
https://www.ncbi.nlm.nih.gov/pubmed/29466982
http://dx.doi.org/10.1186/s12940-018-0361-6
Descripción
Sumario:BACKGROUND: Associations between ambient particulate matter < 2.5 μm (PM(2.5)) and asthma morbidity have been suggested in previous epidemiologic studies but results are inconsistent for areas with lower PM(2.5) levels. We estimated the associations between early-life short-term PM(2.5) exposure and the risk of asthma or wheeze clinical encounters among Massachusetts children in the innovative Pregnancy to Early Life Longitudinal (PELL) cohort data linkage system. METHODS: We used a semi-bidirectional case-crossover study design with short-term exposure lags for asthma exacerbation using data from the PELL system. Cases included children up to 9 years of age who had a hospitalization, observational stay, or emergency department visit for asthma or wheeze between January 2001 and September 2009 (n = 33,387). Daily PM(2.5) concentrations were estimated at a 4-km resolution using satellite remote sensing, land use, and meteorological data. We applied conditional logistic regression models to estimate adjusted odds ratios (ORs) and 95% confidence intervals (CI). We also stratified by potential effect modifiers. RESULTS: The median PM(2.5) concentration among participants was 7.8 μg/m(3) with an interquartile range of 5.9 μg/m(3). Overall, associations between PM(2.5) exposure and asthma clinical encounters among children at lags 0, 1 and 2 were close to the null value of OR = 1.0. Evidence of effect modification was observed by birthweight for lags 0, 1 and 2 (p < 0.05), and season of clinical encounter for lags 0 and 1 (p < 0.05). Children with low birthweight (LBW) (< 2500 g) had increased odds of having an asthma clinical encounter due to higher PM(2.5) exposure for lag 1 (OR: 1.08 per interquartile range (IQR) increase in PM(2.5); 95% CI: 1.01, 1.15). CONCLUSION: Asthma or wheeze exacerbations among LBW children were associated with short-term increases in PM(2.5) concentrations at low levels in Massachusetts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12940-018-0361-6) contains supplementary material, which is available to authorized users.