Persistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhood

Abstract Prenatal exposure to mercury, a known neurotoxic metal, is associated with lower cognitive performance during childhood. Disruption of fetal epigenetic programming could explain mercury’s neurodevelopmental effects. We screened for epigenome-wide methylation differences associated with mate...

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Autores principales: Andres Cardenas, Sheryl L. Rifas-Shiman, Golareh Agha, Marie-France Hivert, Augusto A. Litonjua, Dawn L. DeMeo, Xihong Lin, Chitra J. Amarasiriwardena, Emily Oken, Matthew W. Gillman, Andrea A. Baccarelli
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/34d1f356b4af4b6da9e45b49926acd1a
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spelling oai:doaj.org-article:34d1f356b4af4b6da9e45b49926acd1a2021-12-02T15:06:00ZPersistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhood10.1038/s41598-017-00384-52045-2322https://doaj.org/article/34d1f356b4af4b6da9e45b49926acd1a2017-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-00384-5https://doaj.org/toc/2045-2322Abstract Prenatal exposure to mercury, a known neurotoxic metal, is associated with lower cognitive performance during childhood. Disruption of fetal epigenetic programming could explain mercury’s neurodevelopmental effects. We screened for epigenome-wide methylation differences associated with maternal prenatal blood mercury levels in 321 cord blood DNA samples and examined the persistence of these alterations during early (n = 75; 2.9–4.9 years) and mid-childhood (n = 291; 6.7–10.5 years). Among males, prenatal mercury levels were associated with lower regional cord blood DNA methylation at the Paraoxonase 1 gene (PON1) that persisted in early childhood and was attenuated in mid-childhood blood. Cord blood methylation at the PON1 locus predicted lower cognitive test scores measured during early childhood. Methylation at the PON1 locus was associated with PON1 expression in an independent set of cord blood samples. The observed persistent epigenetic disruption of the PON1 gene may modulate mercury toxicity in humans and might serve as a biomarker of exposure and disease susceptibility.Andres CardenasSheryl L. Rifas-ShimanGolareh AghaMarie-France HivertAugusto A. LitonjuaDawn L. DeMeoXihong LinChitra J. AmarasiriwardenaEmily OkenMatthew W. GillmanAndrea A. BaccarelliNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Andres Cardenas
Sheryl L. Rifas-Shiman
Golareh Agha
Marie-France Hivert
Augusto A. Litonjua
Dawn L. DeMeo
Xihong Lin
Chitra J. Amarasiriwardena
Emily Oken
Matthew W. Gillman
Andrea A. Baccarelli
Persistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhood
description Abstract Prenatal exposure to mercury, a known neurotoxic metal, is associated with lower cognitive performance during childhood. Disruption of fetal epigenetic programming could explain mercury’s neurodevelopmental effects. We screened for epigenome-wide methylation differences associated with maternal prenatal blood mercury levels in 321 cord blood DNA samples and examined the persistence of these alterations during early (n = 75; 2.9–4.9 years) and mid-childhood (n = 291; 6.7–10.5 years). Among males, prenatal mercury levels were associated with lower regional cord blood DNA methylation at the Paraoxonase 1 gene (PON1) that persisted in early childhood and was attenuated in mid-childhood blood. Cord blood methylation at the PON1 locus predicted lower cognitive test scores measured during early childhood. Methylation at the PON1 locus was associated with PON1 expression in an independent set of cord blood samples. The observed persistent epigenetic disruption of the PON1 gene may modulate mercury toxicity in humans and might serve as a biomarker of exposure and disease susceptibility.
format article
author Andres Cardenas
Sheryl L. Rifas-Shiman
Golareh Agha
Marie-France Hivert
Augusto A. Litonjua
Dawn L. DeMeo
Xihong Lin
Chitra J. Amarasiriwardena
Emily Oken
Matthew W. Gillman
Andrea A. Baccarelli
author_facet Andres Cardenas
Sheryl L. Rifas-Shiman
Golareh Agha
Marie-France Hivert
Augusto A. Litonjua
Dawn L. DeMeo
Xihong Lin
Chitra J. Amarasiriwardena
Emily Oken
Matthew W. Gillman
Andrea A. Baccarelli
author_sort Andres Cardenas
title Persistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhood
title_short Persistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhood
title_full Persistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhood
title_fullStr Persistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhood
title_full_unstemmed Persistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhood
title_sort persistent dna methylation changes associated with prenatal mercury exposure and cognitive performance during childhood
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/34d1f356b4af4b6da9e45b49926acd1a
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