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Effects of particulate matter (PM) on childhood asthma exacerbation and control in Xiamen, China
BACKGROUND: The short-term effects of particulate matter (PM) exposure on childhood asthma exacerbation and disease control rate is not thoroughly assessed in Chinese population yet. The previous toxic effects of PM exposure are either based on long-term survey or experimental data from cell lines o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563520/ https://www.ncbi.nlm.nih.gov/pubmed/31196028 http://dx.doi.org/10.1186/s12887-019-1530-7 |
Sumario: | BACKGROUND: The short-term effects of particulate matter (PM) exposure on childhood asthma exacerbation and disease control rate is not thoroughly assessed in Chinese population yet. The previous toxic effects of PM exposure are either based on long-term survey or experimental data from cell lines or mouse models, which also needs to be validated by real-world evidences. METHODS: We evaluated the short-term effects of PM exposure on asthma exacerbation in a Chinese population of 3106 pediatric outpatientsand disease control rate (DCR) in a population of 3344 children using case-crossover design. All the subjects enrolled are non-hospitalized outpatients. All data for this study were collected from the electronic health record (EHR) in the period between January 1, 2016 and June 30, 2018 in Xiamen, China. RESULTS: We found that exposure to PM(2.5) and PM(10) within the past two weeks was significantly associated with elevated risk of exacerbation (OR = 1.049, p < 0.001 for PM(2.5)and OR = 1.027, p < 0.001 for PM(10)). In addition, exposure to PM(10) was associated with decreased DCR (OR = 0.976 for PM(10), p < 0.001). CONCLUSIONS: Our results suggest that exposure to both PM(10) and PM(2.5) has significant short-term effects on childhood asthma exacerbation and DCR, which serves as useful epidemiological parameters for clinical management of asthma risk in the sensitive population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12887-019-1530-7) contains supplementary material, which is available to authorized users. |
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