Can social support during pregnancy affect maternal DNA methylation? Findings from a cohort of African-Americans

Pediatr Res. 2020 Jul;88(1):131-138. doi: 10.1038/s41390-019-0512-7. Epub 2019 Jul 26.

Abstract

Background: While stress and the absence of social support during pregnancy have been linked to poor health outcomes, the underlying biological mechanisms are unclear.

Methods: We examined whether adverse experiences during pregnancy alter DNA methylation (DNAm) in maternal epigenomes. Analyses included 250 African-American mothers from the Boston Birth Cohort. Genome-wide DNAm profiling was performed in maternal blood collected after delivery, using the Infinium HumanMethylation450 Beadchip. Linear regression models, with adjustment of pertinent covariates, were applied.

Results: While self-reported maternal psychosocial lifetime stress and stress during pregnancy was not associated with DNAm alterations, we found that absence of support from the baby's father was significantly associated with maternal DNAm changes in TOR3A, IQCB1, C7orf36, and MYH7B and that lack of support from family and friends was associated with maternal DNA hypermethylation on multiple genes, including PRDM16 and BANKL.

Conclusions: This study provides intriguing results suggesting biological embedding of social support during pregnancy on maternal DNAm, warranting additional investigation, and replication.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adenosine Triphosphatases / genetics
  • Adult
  • Black or African American
  • Boston
  • Calmodulin-Binding Proteins / genetics
  • Cardiac Myosins / genetics
  • CpG Islands
  • DNA Methylation*
  • DNA-Binding Proteins / genetics
  • Epigenome
  • Epigenomics
  • Fathers
  • Female
  • Genome-Wide Association Study
  • Humans
  • Male
  • Membrane Proteins / genetics
  • Minor Histocompatibility Antigens / genetics
  • Molecular Chaperones / genetics
  • Mothers
  • Myosin Heavy Chains / genetics
  • Outcome Assessment, Health Care
  • Pregnancy
  • Premature Birth / epidemiology
  • Premature Birth / ethnology
  • Retrospective Studies
  • Social Class
  • Social Support*
  • Transcription Factors / genetics
  • Urban Population
  • Young Adult

Substances

  • Adaptor Proteins, Signal Transducing
  • BANK1 protein, human
  • Calmodulin-Binding Proteins
  • DNA-Binding Proteins
  • IQCB1 protein, human
  • MYH7 protein, human
  • Membrane Proteins
  • Minor Histocompatibility Antigens
  • Molecular Chaperones
  • PRDM16 protein, human
  • Transcription Factors
  • Adenosine Triphosphatases
  • Cardiac Myosins
  • TOR3A protein, human
  • Myosin Heavy Chains