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Indoor Air Pollution and Outcomes in Cystic Fibrosis

Indoor Air Pollution and Outcomes in Cystic Fibrosis
室内空气污染和囊性纤维化的后果
批准号:
10065102
负责人:
Sara Weller Carson
金额:
$8.74万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-07-02 至 2021-07-01

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PROJECT SUMMARY Cystic Fibrosis (CF) is a lethal autosomal recessive disease affecting nearly 80,000 people worldwide. Despite advances in therapy, CF remains a progressive lung disease that leads to decline in lung function and frequent pulmonary exacerbations. Higher levels of outdoor air pollution, including particulate matter (PM) with a diameter of 10µm or less (PMR10R) and 2.5µm or less (PMR2.5R), nitrogen dioxide (NOR2R), and ozone, have been shown to lead to worse CF outcomes such as decline in lung function and increased pulmonary exacerbations. Many studies have shown that higher levels of indoor air pollution increase morbidity in obstructive lung diseases such as asthma and COPD. To our knowledge, this has not been studied in individuals with CF, also an obstructive lung disease. In this proposal we aim to study how indoor air pollution affects individuals with CF. We hypothesize that higher levels of indoor air pollution are associated with worse CF outcomes, such as increased respiratory symptoms and decline in lung function. To explore our hypothesis, we will conduct a sub-analysis from data collected in the US CF Twin and Sibling Study, which includes data on exposure to sources of indoor air pollution and clinical outcomes on over 2000 CF individuals from 2000-13. Next, we will distribute a survey to our local CF cohort to gather more detailed home exposure data and follow respiratory symptoms and lung function over time. Finally, we will conduct a pilot study to measure daily PMR2.5R and weekly NOR2R and nicotineR Rlevels inside the homes of 20 patients with CF for two one-week periods, separated by season, and ask patients to answer a daily respiratory symptoms questionnaire, complete daily activity diaries, and perform daily home spirometry. We will then determine if daily variations in PMR2.5 Rand weekly levels of NOR2R and nicotine are associated with daily variation in respiratory symptoms and lung function. The research carried out in this proposal is of public health significance and will provide new information on how indoor air pollution affects CF. The results of this study may impact the entire CF community and will serve as a catalyst for a future, multi-center and interventional study which will be the basis for my K23 application.
期刊论文(1)
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DOI: 10.1016/j.jcf.2021.08.015
发表时间: 2022-03
期刊: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
影响因子: --
作者: [Carson SW, Psoter K, Koehler K, Siklosi KR, Montemayor K, Toporek A, West NE, Lechtzin N, Hansel NN, Collaco JM, Merlo CA]
通讯作者: Merlo CA
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