TY - JOUR
T1 - DNA methylation changes associated with prenatal mercury exposure
T2 - A meta-analysis of prospective cohort studies from PACE consortium
AU - Lozano, Manuel
AU - Yousefi, Paul
AU - Broberg, Karin
AU - Soler-Blasco, Raquel
AU - Miyashita, Chihiro
AU - Pesce, Giancarlo
AU - Kim, Woo Jin
AU - Rahman, Mohammad
AU - Bakulski, Kelly M.
AU - Haug, Line S.
AU - Ikeda-Araki, Atsuko
AU - Huel, Guy
AU - Park, Jaehyun
AU - Relton, Caroline
AU - Vrijheid, Martine
AU - Rifas-Shiman, Sheryl
AU - Oken, Emily
AU - Dou, John F.
AU - Kishi, Reiko
AU - Gutzkow, Kristine B.
AU - Annesi-Maesano, Isabella
AU - Won, Sungho
AU - Hivert, Marie France
AU - Fallin, M. Daniele
AU - Vafeiadi, Marina
AU - Ballester, Ferran
AU - Bustamante, Mariona
AU - Llop, Sabrina
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2022/3
Y1 - 2022/3
N2 - Mercury (Hg) is a ubiquitous heavy metal that originates from both natural and anthropogenic sources and is transformed in the environment to its most toxicant form, methylmercury (MeHg). Recent studies suggest that MeHg exposure can alter epigenetic modifications during embryogenesis. In this study, we examined associations between prenatal MeHg exposure and levels of cord blood DNA methylation (DNAm) by meta-analysis in up to seven independent studies (n = 1462) as well as persistence of those relationships in blood from 7 to 8 year-old children (n = 794). In cord blood, we found limited evidence of differential DNAm at cg24184221 in MED31 (β = 2.28 × 10−4, p-value = 5.87 × 10−5) in relation to prenatal MeHg exposure. In child blood, we identified differential DNAm at cg15288800 (β = 0.004, p-value = 4.97 × 10−5), also located in MED31. This repeated link to MED31, a gene involved in lipid metabolism and RNA Polymerase II transcription function, may suggest a DNAm perturbation related to MeHg exposure that persists into early childhood. Further, we found evidence for association between prenatal MeHg exposure and child blood DNAm levels at two additional CpGs: cg12204245 (β = 0.002, p-value = 4.81 × 10−7) in GRK1 and cg02212000 (β = −0.001, p-value = 8.13 × 10−7) in GGH. Prenatal MeHg exposure was associated with DNAm modifications that may influence health outcomes, such as cognitive or anthropometric development, in different populations.
AB - Mercury (Hg) is a ubiquitous heavy metal that originates from both natural and anthropogenic sources and is transformed in the environment to its most toxicant form, methylmercury (MeHg). Recent studies suggest that MeHg exposure can alter epigenetic modifications during embryogenesis. In this study, we examined associations between prenatal MeHg exposure and levels of cord blood DNA methylation (DNAm) by meta-analysis in up to seven independent studies (n = 1462) as well as persistence of those relationships in blood from 7 to 8 year-old children (n = 794). In cord blood, we found limited evidence of differential DNAm at cg24184221 in MED31 (β = 2.28 × 10−4, p-value = 5.87 × 10−5) in relation to prenatal MeHg exposure. In child blood, we identified differential DNAm at cg15288800 (β = 0.004, p-value = 4.97 × 10−5), also located in MED31. This repeated link to MED31, a gene involved in lipid metabolism and RNA Polymerase II transcription function, may suggest a DNAm perturbation related to MeHg exposure that persists into early childhood. Further, we found evidence for association between prenatal MeHg exposure and child blood DNAm levels at two additional CpGs: cg12204245 (β = 0.002, p-value = 4.81 × 10−7) in GRK1 and cg02212000 (β = −0.001, p-value = 8.13 × 10−7) in GGH. Prenatal MeHg exposure was associated with DNAm modifications that may influence health outcomes, such as cognitive or anthropometric development, in different populations.
KW - ALSPAC
KW - DNA methylation
KW - HELIX study
KW - Mercury
KW - Methylmercury
KW - PACE
KW - Prenatal exposure
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U2 - 10.1016/j.envres.2021.112093
DO - 10.1016/j.envres.2021.112093
M3 - Article
C2 - 34562483
AN - SCOPUS:85115779064
SN - 0013-9351
VL - 204
JO - Environmental research
JF - Environmental research
M1 - 112093
ER -