| Literature DB >> 31062658 |
Hudson P Santos1,2, Arjun Bhattacharya3, Elizabeth M Martin4, Kezia Addo4,5, Matt Psioda3, Lisa Smeester2,4,5, Robert M Joseph6, Stephen R Hooper7, Jean A Frazier8,9, Karl C Kuban10, T Michael O'Shea11, Rebecca C Fry2,4,5.
Abstract
This study evaluated the hypothesis that prenatal maternal socioeconomic status (SES) adversity is associated with DNA methylation in the placenta. SES adversity was defined by the presence of, as well as a summative count of, four factors: less than college education, single marital status, food and nutritional service assistance, and public health insurance. Epigenome-wide DNA methylation was assessed using the Illumina EPIC array in 426 placentas from a sample of infants born < 28 weeks of gestation from the Extremely Low Gestational Age Newborn cohort. Associations between SES adversity and DNA methylation were assessed with robust linear regressions adjusted for covariates and controlled the false discovery rate at < 10%. We also examined whether such associations were sex specific. Indicators of SES adversity were associated with differential methylation at 33 CpG sites. Of the 33 identified CpG sites, 19 (57.6%) displayed increased methylation, and 14 (42.4%) displayed decreased methylation in association with at least one of the SES adversity factors. Sex differences were observed in DNA methylation associated with summative SES score; in which placentas derived from female pregnancies showed more robust differential CpG methylation than placentas from male pregnancies. Maternal SES adversity was associated with differential methylation of genes with key role in gene transcription and placental function, potentially altering immunity and stress response. Further investigation is needed to evaluate the role of epigenetic differences in mediating the association between maternal socioeconomic status during pregnancy and later life health outcomes in children.Entities:
Keywords: DNA methylation; Placenta; epigenetics; preterm children; socioeconomic adversity
Mesh:
Year: 2019 PMID: 31062658 PMCID: PMC6615526 DOI: 10.1080/15592294.2019.1614743
Source DB: PubMed Journal: Epigenetics ISSN: 1559-2294 Impact factor: 4.528