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Mediation of the Relationship between Maternal Phthalate Exposure and Preterm Birth by Oxidative Stress with Repeated Measurements across Pregnancy

BACKGROUND: Mediation analysis is useful for understanding mechanisms and has been used minimally in the study of the environment and disease. OBJECTIVE: We examined mediation of the association between phthalate exposure during pregnancy and preterm birth by oxidative stress. METHODS: This nested c...

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Autores principales: Ferguson, Kelly K., Chen, Yin-Hsiu, VanderWeele, Tyler J., McElrath, Thomas F., Meeker, John D., Mukherjee, Bhramar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332184/
https://www.ncbi.nlm.nih.gov/pubmed/27352406
http://dx.doi.org/10.1289/EHP282
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author Ferguson, Kelly K.
Chen, Yin-Hsiu
VanderWeele, Tyler J.
McElrath, Thomas F.
Meeker, John D.
Mukherjee, Bhramar
author_facet Ferguson, Kelly K.
Chen, Yin-Hsiu
VanderWeele, Tyler J.
McElrath, Thomas F.
Meeker, John D.
Mukherjee, Bhramar
author_sort Ferguson, Kelly K.
collection PubMed
description BACKGROUND: Mediation analysis is useful for understanding mechanisms and has been used minimally in the study of the environment and disease. OBJECTIVE: We examined mediation of the association between phthalate exposure during pregnancy and preterm birth by oxidative stress. METHODS: This nested case–control study of preterm birth (n = 130 cases, 352 controls) included women who delivered in Boston, Massachusestts, from 2006 through 2008. Phthalate metabolites and 8-isoprostane, an oxidative stress biomarker, were measured in urine from three visits in pregnancy. We applied four counterfactual mediation methods: method 1, utilizing exposure and mediator averages; method 2, using averages but allowing for an exposure–mediator interaction; method 3, incorporating longitudinal measurements of the exposure and mediator; and method 4, using longitudinal measurements and allowing for an exposure–mediator interaction. RESULTS: We observed mediation of the associations between phthalate metabolites and all preterm birth by 8-isoprostane, with the greatest estimated proportion mediated observed for spontaneous preterm births specifically. Fully utilizing repeated measures of the exposure and mediator improved precision of indirect (i.e., mediated) effect estimates, and including an exposure–mediator interaction increased the estimated proportion mediated. For example, for mono(2-ethyl-carboxy-propyl) phthalate (MECPP), a metabolite of di(2-ethylhexyl) phthalate (DEHP), the percent of the total effect mediated by 8-isoprostane increased from 47% to 60% with inclusion of an exposure–mediator interaction term, in reference to a total adjusted odds ratio of 1.67 or 1.48, respectively. CONCLUSIONS: This demonstrates mediation of the phthalate–preterm birth relationship by oxidative stress, and the utility of complex regression models in capturing mediated associations when repeated measures of exposure and mediator are available and an exposure–mediator interaction may exist. CITATION: Ferguson KK, Chen YH, VanderWeele TJ, McElrath TF, Meeker JD, Mukherjee B. 2017. Mediation of the relationship between maternal phthalate exposure and preterm birth by oxidative stress with repeated measurements across pregnancy. Environ Health Perspect 125:488–494; http://dx.doi.org/10.1289/EHP282
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spelling pubmed-53321842017-03-15 Mediation of the Relationship between Maternal Phthalate Exposure and Preterm Birth by Oxidative Stress with Repeated Measurements across Pregnancy Ferguson, Kelly K. Chen, Yin-Hsiu VanderWeele, Tyler J. McElrath, Thomas F. Meeker, John D. Mukherjee, Bhramar Environ Health Perspect Research BACKGROUND: Mediation analysis is useful for understanding mechanisms and has been used minimally in the study of the environment and disease. OBJECTIVE: We examined mediation of the association between phthalate exposure during pregnancy and preterm birth by oxidative stress. METHODS: This nested case–control study of preterm birth (n = 130 cases, 352 controls) included women who delivered in Boston, Massachusestts, from 2006 through 2008. Phthalate metabolites and 8-isoprostane, an oxidative stress biomarker, were measured in urine from three visits in pregnancy. We applied four counterfactual mediation methods: method 1, utilizing exposure and mediator averages; method 2, using averages but allowing for an exposure–mediator interaction; method 3, incorporating longitudinal measurements of the exposure and mediator; and method 4, using longitudinal measurements and allowing for an exposure–mediator interaction. RESULTS: We observed mediation of the associations between phthalate metabolites and all preterm birth by 8-isoprostane, with the greatest estimated proportion mediated observed for spontaneous preterm births specifically. Fully utilizing repeated measures of the exposure and mediator improved precision of indirect (i.e., mediated) effect estimates, and including an exposure–mediator interaction increased the estimated proportion mediated. For example, for mono(2-ethyl-carboxy-propyl) phthalate (MECPP), a metabolite of di(2-ethylhexyl) phthalate (DEHP), the percent of the total effect mediated by 8-isoprostane increased from 47% to 60% with inclusion of an exposure–mediator interaction term, in reference to a total adjusted odds ratio of 1.67 or 1.48, respectively. CONCLUSIONS: This demonstrates mediation of the phthalate–preterm birth relationship by oxidative stress, and the utility of complex regression models in capturing mediated associations when repeated measures of exposure and mediator are available and an exposure–mediator interaction may exist. CITATION: Ferguson KK, Chen YH, VanderWeele TJ, McElrath TF, Meeker JD, Mukherjee B. 2017. Mediation of the relationship between maternal phthalate exposure and preterm birth by oxidative stress with repeated measurements across pregnancy. Environ Health Perspect 125:488–494; http://dx.doi.org/10.1289/EHP282 National Institute of Environmental Health Sciences 2016-06-28 2017-03 /pmc/articles/PMC5332184/ /pubmed/27352406 http://dx.doi.org/10.1289/EHP282 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, “Reproduced with permission from Environmental Health Perspectives”); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Ferguson, Kelly K.
Chen, Yin-Hsiu
VanderWeele, Tyler J.
McElrath, Thomas F.
Meeker, John D.
Mukherjee, Bhramar
Mediation of the Relationship between Maternal Phthalate Exposure and Preterm Birth by Oxidative Stress with Repeated Measurements across Pregnancy
title Mediation of the Relationship between Maternal Phthalate Exposure and Preterm Birth by Oxidative Stress with Repeated Measurements across Pregnancy
title_full Mediation of the Relationship between Maternal Phthalate Exposure and Preterm Birth by Oxidative Stress with Repeated Measurements across Pregnancy
title_fullStr Mediation of the Relationship between Maternal Phthalate Exposure and Preterm Birth by Oxidative Stress with Repeated Measurements across Pregnancy
title_full_unstemmed Mediation of the Relationship between Maternal Phthalate Exposure and Preterm Birth by Oxidative Stress with Repeated Measurements across Pregnancy
title_short Mediation of the Relationship between Maternal Phthalate Exposure and Preterm Birth by Oxidative Stress with Repeated Measurements across Pregnancy
title_sort mediation of the relationship between maternal phthalate exposure and preterm birth by oxidative stress with repeated measurements across pregnancy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332184/
https://www.ncbi.nlm.nih.gov/pubmed/27352406
http://dx.doi.org/10.1289/EHP282
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