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Global Effect Factors for Exposure to Fine Particulate Matter
[Image: see text] We evaluate fine particulate matter (PM(2.5)) exposure–response models to propose a consistent set of global effect factors for product and policy assessments across spatial scales and across urban and rural environments. Relationships among exposure concentrations and PM(2.5)-attr...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613786/ https://www.ncbi.nlm.nih.gov/pubmed/31132267 http://dx.doi.org/10.1021/acs.est.9b01800 |
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author | Fantke, Peter McKone, Thomas E. Tainio, Marko Jolliet, Olivier Apte, Joshua S. Stylianou, Katerina S. Illner, Nicole Marshall, Julian D. Choma, Ernani F. Evans, John S. |
author_facet | Fantke, Peter McKone, Thomas E. Tainio, Marko Jolliet, Olivier Apte, Joshua S. Stylianou, Katerina S. Illner, Nicole Marshall, Julian D. Choma, Ernani F. Evans, John S. |
author_sort | Fantke, Peter |
collection | PubMed |
description | [Image: see text] We evaluate fine particulate matter (PM(2.5)) exposure–response models to propose a consistent set of global effect factors for product and policy assessments across spatial scales and across urban and rural environments. Relationships among exposure concentrations and PM(2.5)-attributable health effects largely depend on location, population density, and mortality rates. Existing effect factors build mostly on an essentially linear exposure–response function with coefficients from the American Cancer Society study. In contrast, the Global Burden of Disease analysis offers a nonlinear integrated exposure–response (IER) model with coefficients derived from numerous epidemiological studies covering a wide range of exposure concentrations. We explore the IER, additionally provide a simplified regression as a function of PM(2.5) level, mortality rates, and severity, and compare results with effect factors derived from the recently published global exposure mortality model (GEMM). Uncertainty in effect factors is dominated by the exposure–response shape, background mortality, and geographic variability. Our central IER-based effect factor estimates for different regions do not differ substantially from previous estimates. However, IER estimates exhibit significant variability between locations as well as between urban and rural environments, driven primarily by variability in PM(2.5) concentrations and mortality rates. Using the IER as the basis for effect factors presents a consistent picture of global PM(2.5)-related effects for use in product and policy assessment frameworks. |
format | Online Article Text |
id | pubmed-6613786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66137862019-07-09 Global Effect Factors for Exposure to Fine Particulate Matter Fantke, Peter McKone, Thomas E. Tainio, Marko Jolliet, Olivier Apte, Joshua S. Stylianou, Katerina S. Illner, Nicole Marshall, Julian D. Choma, Ernani F. Evans, John S. Environ Sci Technol [Image: see text] We evaluate fine particulate matter (PM(2.5)) exposure–response models to propose a consistent set of global effect factors for product and policy assessments across spatial scales and across urban and rural environments. Relationships among exposure concentrations and PM(2.5)-attributable health effects largely depend on location, population density, and mortality rates. Existing effect factors build mostly on an essentially linear exposure–response function with coefficients from the American Cancer Society study. In contrast, the Global Burden of Disease analysis offers a nonlinear integrated exposure–response (IER) model with coefficients derived from numerous epidemiological studies covering a wide range of exposure concentrations. We explore the IER, additionally provide a simplified regression as a function of PM(2.5) level, mortality rates, and severity, and compare results with effect factors derived from the recently published global exposure mortality model (GEMM). Uncertainty in effect factors is dominated by the exposure–response shape, background mortality, and geographic variability. Our central IER-based effect factor estimates for different regions do not differ substantially from previous estimates. However, IER estimates exhibit significant variability between locations as well as between urban and rural environments, driven primarily by variability in PM(2.5) concentrations and mortality rates. Using the IER as the basis for effect factors presents a consistent picture of global PM(2.5)-related effects for use in product and policy assessment frameworks. American Chemical Society 2019-05-27 2019-06-18 /pmc/articles/PMC6613786/ /pubmed/31132267 http://dx.doi.org/10.1021/acs.est.9b01800 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Fantke, Peter McKone, Thomas E. Tainio, Marko Jolliet, Olivier Apte, Joshua S. Stylianou, Katerina S. Illner, Nicole Marshall, Julian D. Choma, Ernani F. Evans, John S. Global Effect Factors for Exposure to Fine Particulate Matter |
title | Global
Effect Factors for Exposure to Fine Particulate
Matter |
title_full | Global
Effect Factors for Exposure to Fine Particulate
Matter |
title_fullStr | Global
Effect Factors for Exposure to Fine Particulate
Matter |
title_full_unstemmed | Global
Effect Factors for Exposure to Fine Particulate
Matter |
title_short | Global
Effect Factors for Exposure to Fine Particulate
Matter |
title_sort | global
effect factors for exposure to fine particulate
matter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613786/ https://www.ncbi.nlm.nih.gov/pubmed/31132267 http://dx.doi.org/10.1021/acs.est.9b01800 |
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