Maternal cadmium, iron and zinc levels, DNA methylation and birth weight.

Journal Article (Journal Article)

BACKGROUND: Cadmium (Cd) is a ubiquitous and environmentally persistent toxic metal that has been implicated in neurotoxicity, carcinogenesis and obesity and essential metals including zinc (Zn) and iron (Fe) may alter these outcomes. However mechanisms underlying these relationships remain limited. METHODS: We examined whether maternal Cd levels during early pregnancy were associated with offspring DNA methylation at regulatory sequences of genomically imprinted genes and weight at birth, and whether Fe and Zn altered these associations. Cd, Fe and Zn were measured in maternal blood of 319 women ≤ 12 weeks gestation. Offspring umbilical cord blood leukocyte DNA methylation at regulatory differentially methylated regions (DMRs) of 8 imprinted genes was measured using bisulfite pyrosequencing. Regression models were used to examine the relationships among Cd, Fe, Zn, and DMR methylation and birth weight. RESULTS: Elevated maternal blood Cd levels were associated with lower birth weight (p = 0.03). Higher maternal blood Cd levels were also associated with lower offspring methylation at the PEG3 DMR in females (β = 0.55, se = 0.17, p = 0.05), and at the MEG3 DMR in males (β = 0.72, se = 0.3, p = 0.08), however the latter association was not statistically significant. Associations between Cd and PEG3 and PLAGL1 DNA methylation were stronger in infants born to women with low concentrations of Fe (p < 0.05). CONCLUSIONS: Our data suggest the association between pre-natal Cd and offspring DNA methylation at regulatory sequences of imprinted genes may be sex- and gene-specific. Essential metals such as Zn may mitigate DNA methylation response to Cd exposure. Larger studies are required.

Full Text

Duke Authors

Cited Authors

  • Vidal, AC; Semenova, V; Darrah, T; Vengosh, A; Huang, Z; King, K; Nye, MD; Fry, R; Skaar, D; Maguire, R; Murtha, A; Schildkraut, J; Murphy, S; Hoyo, C

Published Date

  • July 15, 2015

Published In

Volume / Issue

  • 16 /

Start / End Page

  • 20 -

PubMed ID

  • 26173596

Pubmed Central ID

  • PMC4502530

Electronic International Standard Serial Number (EISSN)

  • 2050-6511

Digital Object Identifier (DOI)

  • 10.1186/s40360-015-0020-2


  • eng

Conference Location

  • England