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 inChest Vol. 153; no. 5; p. 1221
Main Authors Winterbottom, Christopher J, Shah, Rupal J, Patterson, Karen C, Kreider, Maryl E, Panettieri, Jr, Reynold A, Rivera-Lebron, Belinda, Miller, Wallace T, Litzky, Leslie A, Penning, Trevor M, Heinlen, Krista, Jackson, Tara, Localio, A Russell, Christie, Jason D
Format Journal Article
LanguageEnglish
Published 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.
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
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  surname: Winterbottom
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  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
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  organization: Division of Pulmonary, Critical Care, Allergy, and Sleep Medicine, University of California, San Francisco, San Francisco, CA
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  surname: Patterson
  fullname: Patterson, Karen C
  organization: Division of Pulmonary, Allergy, and Critical Care Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
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  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
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  surname: Panettieri, Jr
  fullname: Panettieri, Jr, Reynold A
  organization: Department of Medicine, Rutgers Biomedical and Health Sciences University, New Brunswick, NJ
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  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
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  surname: Miller
  fullname: Miller, Wallace T
  organization: Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
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  surname: Litzky
  fullname: Litzky, Leslie A
  organization: Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
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  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
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  givenname: Krista
  surname: Heinlen
  fullname: Heinlen, Krista
  organization: Cartographic Modeling Laboratory, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
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  surname: Jackson
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  organization: Cartographic Modeling Laboratory, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
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  surname: Localio
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  surname: Christie
  fullname: Christie, Jason D
  organization: Division of Pulmonary, Allergy, and Critical Care Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
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Keywords air pollution
idiopathic pulmonary fibrosis
interstitial lung disease
environmental pollution
pulmonary fibrosis
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Snippet Idiopathic pulmonary fibrosis (IPF), a progressive disease with an unknown pathogenesis, may be due in part to an abnormal response to injurious stimuli by...
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Title Exposure to Ambient Particulate Matter Is Associated With Accelerated Functional Decline in Idiopathic Pulmonary Fibrosis
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