Epigenetics of Trauma Transmission and Fetal Alcohol Spectrum Disorder: What Does the Evidence Support?

Int J Environ Res Public Health. 2023 Sep 3;20(17):6706. doi: 10.3390/ijerph20176706.

Abstract

Fetal alcohol spectrum disorder (FASD) results from teratogenic impacts of alcohol consumption during pregnancy. Trauma and prenatal alcohol exposure (PAE) can both cause neurodevelopmental impairment, and it has been proposed that FASD can amplify effects of trauma. Certain PAE and trauma effects are mediated via epigenetic mechanisms. The objective of this review is to present the current evidence for epigenetics in trauma transmission as it relates to FASD, to help bridge a potential knowledge gap for social workers and related health professionals. We include a primer on epigenetic mechanisms and inheritance, followed by a summary of the current biomedical evidence supporting intergenerational and transgenerational epigenetic transmission of trauma, its relevance to FASD, the intersection with social transmission, and finally the application to social work. We propose potential models of transmission, considering where social and epigenetic pathways may intersect and/or compound across generations. Overall, we aim to provide a better understanding of epigenetic-trauma transmission for its application to health professions, in particular which beliefs are (and are not) evidence-based. We discuss the lack of research and challenges of studying epigenetic transmission in humans and identify the need for public health interventions and best practices that are based on the current evidence.

Keywords: FASD; PAE; epigenetic inheritance; epigenetics; fetal alcohol spectrum disorder; intergenerational trauma; prenatal alcohol exposure; social work; transgenerational trauma; trauma.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Drinking
  • Epigenesis, Genetic
  • Female
  • Fetal Alcohol Spectrum Disorders* / genetics
  • Humans
  • Pregnancy
  • Prenatal Exposure Delayed Effects* / genetics
  • Public Health

Grants and funding

This research was funded by Mount Royal University Internal Research Grant #102679. The APC was funded by Mount Royal University Internal Research Grant #102679.