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Relative toxicities of major particulate matter constituents on birthweight in Massachusetts

BACKGROUND: Maternal exposure to fine particulate air pollution (PM(2.5)) during pregnancy has been linked to lower newborn birthweight, making it a toxic exposure because lower birthweight is a risk factor for chronic disease and mortality. However, the toxicity of major constituents of PM(2.5) and...

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Autores principales: Fong, Kelvin C., Di, Qian, Kloog, Itai, Laden, Francine, Coull, Brent A., Koutrakis, Petros, Schwartz, Joel D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571180/
https://www.ncbi.nlm.nih.gov/pubmed/31342007
http://dx.doi.org/10.1097/EE9.0000000000000047
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author Fong, Kelvin C.
Di, Qian
Kloog, Itai
Laden, Francine
Coull, Brent A.
Koutrakis, Petros
Schwartz, Joel D.
author_facet Fong, Kelvin C.
Di, Qian
Kloog, Itai
Laden, Francine
Coull, Brent A.
Koutrakis, Petros
Schwartz, Joel D.
author_sort Fong, Kelvin C.
collection PubMed
description BACKGROUND: Maternal exposure to fine particulate air pollution (PM(2.5)) during pregnancy has been linked to lower newborn birthweight, making it a toxic exposure because lower birthweight is a risk factor for chronic disease and mortality. However, the toxicity of major constituents of PM(2.5) and how they compare to each other remain uncertain. METHODS: We assigned address-specific exposure to PM(2.5), elemental carbon (EC), organic carbon (OC), nitrate, and sulfate averaged over the entire period of pregnancy for each birth in Massachusetts from 2001 to 2012 using a high-resolution exposure model. Using multivariate regression adjusted for total PM(2.5), we estimated the relative toxicity of each constituent on continuous birthweight. RESULTS: EC was more toxic per interquartile range increase compared with remaining PM(2.5) in single constituent models that estimated the effect of a constituent with adjustment for PM(2.5). OC, nitrate, and sulfate were each less toxic than their respective remaining PM(2.5) per interquartile range increase. When all constituents and total PM(2.5) were included in the same model, EC was most toxic, followed by nitrate, then OC and sulfate with similar toxicities. Sensitivity analyses using term low birth weight and small for gestational age also showed that EC was most detrimental as did averaging exposures over the third trimester of pregnancy. Scaling to unit mass increases also showed EC to be most toxic. CONCLUSION: Four major constituents of PM(2.5) had different relative toxicities on continuous birthweight. Our findings suggest that EC was most toxic, followed by nitrate, OC, and sulfate.
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spelling pubmed-65711802019-07-22 Relative toxicities of major particulate matter constituents on birthweight in Massachusetts Fong, Kelvin C. Di, Qian Kloog, Itai Laden, Francine Coull, Brent A. Koutrakis, Petros Schwartz, Joel D. Environ Epidemiol Original Research BACKGROUND: Maternal exposure to fine particulate air pollution (PM(2.5)) during pregnancy has been linked to lower newborn birthweight, making it a toxic exposure because lower birthweight is a risk factor for chronic disease and mortality. However, the toxicity of major constituents of PM(2.5) and how they compare to each other remain uncertain. METHODS: We assigned address-specific exposure to PM(2.5), elemental carbon (EC), organic carbon (OC), nitrate, and sulfate averaged over the entire period of pregnancy for each birth in Massachusetts from 2001 to 2012 using a high-resolution exposure model. Using multivariate regression adjusted for total PM(2.5), we estimated the relative toxicity of each constituent on continuous birthweight. RESULTS: EC was more toxic per interquartile range increase compared with remaining PM(2.5) in single constituent models that estimated the effect of a constituent with adjustment for PM(2.5). OC, nitrate, and sulfate were each less toxic than their respective remaining PM(2.5) per interquartile range increase. When all constituents and total PM(2.5) were included in the same model, EC was most toxic, followed by nitrate, then OC and sulfate with similar toxicities. Sensitivity analyses using term low birth weight and small for gestational age also showed that EC was most detrimental as did averaging exposures over the third trimester of pregnancy. Scaling to unit mass increases also showed EC to be most toxic. CONCLUSION: Four major constituents of PM(2.5) had different relative toxicities on continuous birthweight. Our findings suggest that EC was most toxic, followed by nitrate, OC, and sulfate. Wolters Kluwer Health 2019-04-09 /pmc/articles/PMC6571180/ /pubmed/31342007 http://dx.doi.org/10.1097/EE9.0000000000000047 Text en Copyright © 2019 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of Environmental Epidemiology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Original Research
Fong, Kelvin C.
Di, Qian
Kloog, Itai
Laden, Francine
Coull, Brent A.
Koutrakis, Petros
Schwartz, Joel D.
Relative toxicities of major particulate matter constituents on birthweight in Massachusetts
title Relative toxicities of major particulate matter constituents on birthweight in Massachusetts
title_full Relative toxicities of major particulate matter constituents on birthweight in Massachusetts
title_fullStr Relative toxicities of major particulate matter constituents on birthweight in Massachusetts
title_full_unstemmed Relative toxicities of major particulate matter constituents on birthweight in Massachusetts
title_short Relative toxicities of major particulate matter constituents on birthweight in Massachusetts
title_sort relative toxicities of major particulate matter constituents on birthweight in massachusetts
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571180/
https://www.ncbi.nlm.nih.gov/pubmed/31342007
http://dx.doi.org/10.1097/EE9.0000000000000047
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