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Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects
BACKGROUND: In utero exposure to particulate matter with an aerodynamic diameter of less than 2.5 μm (PM(2.5)) has been linked to child lung function. Overlapping evidence suggests that child sex and exposure timing may modify effects and associations may be mediated through glutathione S-transferas...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923186/ https://www.ncbi.nlm.nih.gov/pubmed/29703190 http://dx.doi.org/10.1186/s12931-018-0774-3 |
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author | Lee, Alison G. Le Grand, Blake Hsu, Hsiao-Hsien Leon Chiu, Yueh-Hsiu Mathilda Brennan, Kasey J. Bose, Sonali Rosa, Maria José Brunst, Kelly J. Kloog, Itai Wilson, Ander Schwartz, Joel Morgan, Wayne Coull, Brent A. Wright, Robert O. Baccarelli, Andrea A. Wright, Rosalind J. |
author_facet | Lee, Alison G. Le Grand, Blake Hsu, Hsiao-Hsien Leon Chiu, Yueh-Hsiu Mathilda Brennan, Kasey J. Bose, Sonali Rosa, Maria José Brunst, Kelly J. Kloog, Itai Wilson, Ander Schwartz, Joel Morgan, Wayne Coull, Brent A. Wright, Robert O. Baccarelli, Andrea A. Wright, Rosalind J. |
author_sort | Lee, Alison G. |
collection | PubMed |
description | BACKGROUND: In utero exposure to particulate matter with an aerodynamic diameter of less than 2.5 μm (PM(2.5)) has been linked to child lung function. Overlapping evidence suggests that child sex and exposure timing may modify effects and associations may be mediated through glutathione S-transferase P1 (GSTP1) methylation. METHODS: We prospectively examined associations among prenatal PM(2.5) exposure and child lung function and GSTP1 methylation in an urban pregnancy cohort study. We employed a validated satellite-based spatiotemporally resolved prediction model to estimate daily prenatal PM(2.5) exposure over gestation. We used Baysian distributed lag interaction models (BDLIMs) to identify sensitive windows for prenatal PM(2.5) exposure on child lung function and nasal epithelia GSTP1 methylation at age 7 years, and to examine effect modification by child sex. RESULTS: BDLIMs identified a sensitive window for prenatal PM(2.5) exposure at 35–40 weeks gestation [cumulative effect estimate (CEE) = − 0.10, 95%CI = − 0.19 to − 0.01, per μg/m(3) increase in PM(2.5)] and at 36–40 weeks (CEE = − 0.12, 95%CI = − 0.20 to − 0.01) on FEV(1) and FVC, respectively, in boys. BDLIMs also identified a sensitive window of exposure at 37–40 weeks gestation between higher prenatal PM(2.5) exposure and increased GSTP1 percent methylation. The association between higher GSTP1 percent methylation and decreased FEV1 was borderline significant in the sample as a whole (β = − 0.37, SE = 0.20, p = 0.06) and in boys in stratified analyses (β = − 0.56, SE = 0.29, p = 0.05). CONCLUSIONS: Prenatal PM(2.5) exposure in late pregnancy was associated with impaired early childhood lung function and hypermethylation of GSTPI in DNA isolated from nasal epithelial cells. There was a trend towards higher GSTP1 percent methylation being associated with reduced FEV1. All findings were most evident among boys. |
format | Online Article Text |
id | pubmed-5923186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59231862018-05-01 Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects Lee, Alison G. Le Grand, Blake Hsu, Hsiao-Hsien Leon Chiu, Yueh-Hsiu Mathilda Brennan, Kasey J. Bose, Sonali Rosa, Maria José Brunst, Kelly J. Kloog, Itai Wilson, Ander Schwartz, Joel Morgan, Wayne Coull, Brent A. Wright, Robert O. Baccarelli, Andrea A. Wright, Rosalind J. Respir Res Research BACKGROUND: In utero exposure to particulate matter with an aerodynamic diameter of less than 2.5 μm (PM(2.5)) has been linked to child lung function. Overlapping evidence suggests that child sex and exposure timing may modify effects and associations may be mediated through glutathione S-transferase P1 (GSTP1) methylation. METHODS: We prospectively examined associations among prenatal PM(2.5) exposure and child lung function and GSTP1 methylation in an urban pregnancy cohort study. We employed a validated satellite-based spatiotemporally resolved prediction model to estimate daily prenatal PM(2.5) exposure over gestation. We used Baysian distributed lag interaction models (BDLIMs) to identify sensitive windows for prenatal PM(2.5) exposure on child lung function and nasal epithelia GSTP1 methylation at age 7 years, and to examine effect modification by child sex. RESULTS: BDLIMs identified a sensitive window for prenatal PM(2.5) exposure at 35–40 weeks gestation [cumulative effect estimate (CEE) = − 0.10, 95%CI = − 0.19 to − 0.01, per μg/m(3) increase in PM(2.5)] and at 36–40 weeks (CEE = − 0.12, 95%CI = − 0.20 to − 0.01) on FEV(1) and FVC, respectively, in boys. BDLIMs also identified a sensitive window of exposure at 37–40 weeks gestation between higher prenatal PM(2.5) exposure and increased GSTP1 percent methylation. The association between higher GSTP1 percent methylation and decreased FEV1 was borderline significant in the sample as a whole (β = − 0.37, SE = 0.20, p = 0.06) and in boys in stratified analyses (β = − 0.56, SE = 0.29, p = 0.05). CONCLUSIONS: Prenatal PM(2.5) exposure in late pregnancy was associated with impaired early childhood lung function and hypermethylation of GSTPI in DNA isolated from nasal epithelial cells. There was a trend towards higher GSTP1 percent methylation being associated with reduced FEV1. All findings were most evident among boys. BioMed Central 2018-04-27 2018 /pmc/articles/PMC5923186/ /pubmed/29703190 http://dx.doi.org/10.1186/s12931-018-0774-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lee, Alison G. Le Grand, Blake Hsu, Hsiao-Hsien Leon Chiu, Yueh-Hsiu Mathilda Brennan, Kasey J. Bose, Sonali Rosa, Maria José Brunst, Kelly J. Kloog, Itai Wilson, Ander Schwartz, Joel Morgan, Wayne Coull, Brent A. Wright, Robert O. Baccarelli, Andrea A. Wright, Rosalind J. Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects |
title | Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects |
title_full | Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects |
title_fullStr | Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects |
title_full_unstemmed | Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects |
title_short | Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects |
title_sort | prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia gstp1 hypermethylation: sex-specific effects |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923186/ https://www.ncbi.nlm.nih.gov/pubmed/29703190 http://dx.doi.org/10.1186/s12931-018-0774-3 |
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