Exposure to Ambient Particulate Matter Is Associated With Accelerated Functional Decline in Idiopathic Pulmonary Fibrosis
Idiopathic pulmonary fibrosis (IPF), a progressive disease with an unknown pathogenesis, may be due in part to an abnormal response to injurious stimuli by alveolar epithelial cells. Air pollution and particulate inhalation of matter evoke a wide variety of pulmonary and systemic inflammatory diseas...
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Published in | Chest Vol. 153; no. 5; p. 1221 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
01.05.2018
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Abstract | Idiopathic pulmonary fibrosis (IPF), a progressive disease with an unknown pathogenesis, may be due in part to an abnormal response to injurious stimuli by alveolar epithelial cells. Air pollution and particulate inhalation of matter evoke a wide variety of pulmonary and systemic inflammatory diseases. We therefore hypothesized that increased average ambient particulate matter (PM) concentrations would be associated with an accelerated rate of decline in FVC in IPF.
We identified a cohort of subjects seen at a single university referral center from 2007 to 2013. Average concentrations of particulate matter < 10 and < 2.5 μg/m
(PM
and PM
, respectively) were assigned to each patient based on geocoded residential addresses. A linear multivariable mixed-effects model determined the association between the rate of decline in FVC and average PM concentration, controlling for baseline FVC at first measurement and other covariates.
One hundred thirty-five subjects were included in the final analysis after exclusion of subjects missing repeated spirometry measurements and those for whom exposure data were not available. There was a significant association between PM
levels and the rate of decline in FVC during the study period, with each μg/m
increase in PM
corresponding with an additional 46 cc/y decline in FVC (P = .008).
Ambient air pollution, as measured by average PM
concentration, is associated with an increase in the rate of decline of FVC in IPF, suggesting a potential mechanistic role for air pollution in the progression of disease. |
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AbstractList | Idiopathic pulmonary fibrosis (IPF), a progressive disease with an unknown pathogenesis, may be due in part to an abnormal response to injurious stimuli by alveolar epithelial cells. Air pollution and particulate inhalation of matter evoke a wide variety of pulmonary and systemic inflammatory diseases. We therefore hypothesized that increased average ambient particulate matter (PM) concentrations would be associated with an accelerated rate of decline in FVC in IPF.
We identified a cohort of subjects seen at a single university referral center from 2007 to 2013. Average concentrations of particulate matter < 10 and < 2.5 μg/m
(PM
and PM
, respectively) were assigned to each patient based on geocoded residential addresses. A linear multivariable mixed-effects model determined the association between the rate of decline in FVC and average PM concentration, controlling for baseline FVC at first measurement and other covariates.
One hundred thirty-five subjects were included in the final analysis after exclusion of subjects missing repeated spirometry measurements and those for whom exposure data were not available. There was a significant association between PM
levels and the rate of decline in FVC during the study period, with each μg/m
increase in PM
corresponding with an additional 46 cc/y decline in FVC (P = .008).
Ambient air pollution, as measured by average PM
concentration, is associated with an increase in the rate of decline of FVC in IPF, suggesting a potential mechanistic role for air pollution in the progression of disease. |
Author | Jackson, Tara Litzky, Leslie A Rivera-Lebron, Belinda Kreider, Maryl E Miller, Wallace T Patterson, Karen C Penning, Trevor M Winterbottom, Christopher J Heinlen, Krista Localio, A Russell Shah, Rupal J Christie, Jason D Panettieri, Jr, Reynold A |
Author_xml | – sequence: 1 givenname: Christopher J surname: Winterbottom fullname: Winterbottom, Christopher J email: christopher.winterbottom@yale.edu organization: Section of Pulmonary, Critical Care and Sleep Medicine, Yale University School of Medicine, Yale University, New Haven, CT. Electronic address: christopher.winterbottom@yale.edu – sequence: 2 givenname: Rupal J surname: Shah fullname: Shah, Rupal J organization: Division of Pulmonary, Critical Care, Allergy, and Sleep Medicine, University of California, San Francisco, San Francisco, CA – sequence: 3 givenname: Karen C surname: Patterson fullname: Patterson, Karen C organization: Division of Pulmonary, Allergy, and Critical Care Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA – sequence: 4 givenname: Maryl E surname: Kreider fullname: Kreider, Maryl E organization: Division of Pulmonary, Allergy, and Critical Care Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA – sequence: 5 givenname: Reynold A surname: Panettieri, Jr fullname: Panettieri, Jr, Reynold A organization: Department of Medicine, Rutgers Biomedical and Health Sciences University, New Brunswick, NJ – sequence: 6 givenname: Belinda surname: Rivera-Lebron fullname: Rivera-Lebron, Belinda organization: Division of Pulmonary, Allergy, and Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA – sequence: 7 givenname: Wallace T surname: Miller fullname: Miller, Wallace T organization: Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA – sequence: 8 givenname: Leslie A surname: Litzky fullname: Litzky, Leslie A organization: Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA – sequence: 9 givenname: Trevor M surname: Penning fullname: Penning, Trevor M organization: Center of Excellence in Environmental Toxicology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA – sequence: 10 givenname: Krista surname: Heinlen fullname: Heinlen, Krista organization: Cartographic Modeling Laboratory, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA – sequence: 11 givenname: Tara surname: Jackson fullname: Jackson, Tara organization: Cartographic Modeling Laboratory, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA – sequence: 12 givenname: A Russell surname: Localio fullname: Localio, A Russell organization: Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA – sequence: 13 givenname: Jason D surname: Christie fullname: Christie, Jason D organization: Division of Pulmonary, Allergy, and Critical Care Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28802694$$D View this record in MEDLINE/PubMed |
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Copyright | Copyright © 2017 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved. |
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Keywords | air pollution idiopathic pulmonary fibrosis interstitial lung disease environmental pollution pulmonary fibrosis |
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Title | Exposure to Ambient Particulate Matter Is Associated With Accelerated Functional Decline in Idiopathic Pulmonary Fibrosis |
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