Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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
_version_ 1783318281382264832
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
work_keys_str_mv AT leealisong prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT legrandblake prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT hsuhsiaohsienleon prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT chiuyuehhsiumathilda prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT brennankaseyj prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT bosesonali prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT rosamariajose prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT brunstkellyj prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT kloogitai prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT wilsonander prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT schwartzjoel prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT morganwayne prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT coullbrenta prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT wrightroberto prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT baccarelliandreaa prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects
AT wrightrosalindj prenatalfineparticulateexposureassociatedwithreducedchildhoodlungfunctionandnasalepitheliagstp1hypermethylationsexspecificeffects