{"title":"Associations of ambient fine particulate matter with lung function and nasal microbiota: A panel study in asthmatic children","authors":"Chang Huang, Wen He, Lijuan Liu, Xiao Han, Yuan Yuan, Jianfeng Huang, Fang Liu, Qinglin He, Haidong Kan, Renjie Chen, Xiaobo Zhang, Yue Niu","doi":"10.1016/j.envpol.2025.126084","DOIUrl":null,"url":null,"abstract":"Fine particulate matter (PM<sub>2.5</sub>) has been associated with an increased risk of asthma. However, the underlying mechanisms through which PM<sub>2.5</sub> affects respiratory health in children with asthma remain poorly understood. To address this gap, we performed a panel study to investigate the associations of short-term PM<sub>2.5</sub> exposure with lung function and nasal microbiota in asthmatic children. The study included 50 school-aged asthmatic children, who underwent repeated examinations every three months, including lung function testing and nasal swab sample collection. Linear mixed-effect models and the linear discriminant analysis effect size were adopted to evaluate the impacts of PM<sub>2.5</sub> on lung function and nasal microbiota. Based on 160 lung function records and 160 nasal samples, we found that per interquartile range increase in PM<sub>2.5</sub> concentration at lag 0–72 h was associated with a decrease of 0.09 L (95% CI: 0.01, 0.16), 0.30 L/s (95 CI: 0.04, 0.57), 0.18 L/s (95% CI: 0.03, 0.33), and 0.30 L/s (95% CI: 0.07, 0.53) in forced expiratory volume in 1 second, forced expiratory flow at 50% and 75% of forced vital capacity, and the maximal mid-expiratory flow, respectively. Additionally, short-term exposure to PM<sub>2.5</sub> was also associated with decreased Chao 1 and Simpson’s index, decreased relative abundance in <em>Corynebacterium</em> and <em>Staphylococcus</em>, and increased relative abundance in <em>Muribaculaceae</em>, <em>Ralstonia</em>, and <em>Moraxella</em>. In conclusion, our study demonstrated that short-term exposure to PM<sub>2.5</sub> may impair small airway function, reduce nasal microbiota evenness, and induce microbiota dysbiosis in asthmatic children.","PeriodicalId":311,"journal":{"name":"Environmental Pollution","volume":"18 1","pages":""},"PeriodicalIF":7.6000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Pollution","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1016/j.envpol.2025.126084","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Fine particulate matter (PM2.5) has been associated with an increased risk of asthma. However, the underlying mechanisms through which PM2.5 affects respiratory health in children with asthma remain poorly understood. To address this gap, we performed a panel study to investigate the associations of short-term PM2.5 exposure with lung function and nasal microbiota in asthmatic children. The study included 50 school-aged asthmatic children, who underwent repeated examinations every three months, including lung function testing and nasal swab sample collection. Linear mixed-effect models and the linear discriminant analysis effect size were adopted to evaluate the impacts of PM2.5 on lung function and nasal microbiota. Based on 160 lung function records and 160 nasal samples, we found that per interquartile range increase in PM2.5 concentration at lag 0–72 h was associated with a decrease of 0.09 L (95% CI: 0.01, 0.16), 0.30 L/s (95 CI: 0.04, 0.57), 0.18 L/s (95% CI: 0.03, 0.33), and 0.30 L/s (95% CI: 0.07, 0.53) in forced expiratory volume in 1 second, forced expiratory flow at 50% and 75% of forced vital capacity, and the maximal mid-expiratory flow, respectively. Additionally, short-term exposure to PM2.5 was also associated with decreased Chao 1 and Simpson’s index, decreased relative abundance in Corynebacterium and Staphylococcus, and increased relative abundance in Muribaculaceae, Ralstonia, and Moraxella. In conclusion, our study demonstrated that short-term exposure to PM2.5 may impair small airway function, reduce nasal microbiota evenness, and induce microbiota dysbiosis in asthmatic children.
期刊介绍:
Environmental Pollution is an international peer-reviewed journal that publishes high-quality research papers and review articles covering all aspects of environmental pollution and its impacts on ecosystems and human health.
Subject areas include, but are not limited to:
• Sources and occurrences of pollutants that are clearly defined and measured in environmental compartments, food and food-related items, and human bodies;
• Interlinks between contaminant exposure and biological, ecological, and human health effects, including those of climate change;
• Contaminants of emerging concerns (including but not limited to antibiotic resistant microorganisms or genes, microplastics/nanoplastics, electronic wastes, light, and noise) and/or their biological, ecological, or human health effects;
• Laboratory and field studies on the remediation/mitigation of environmental pollution via new techniques and with clear links to biological, ecological, or human health effects;
• Modeling of pollution processes, patterns, or trends that is of clear environmental and/or human health interest;
• New techniques that measure and examine environmental occurrences, transport, behavior, and effects of pollutants within the environment or the laboratory, provided that they can be clearly used to address problems within regional or global environmental compartments.