Role of oxidative stress, genome damage and DNA methylation as determinants of pathological conditions in the newborn: an overview from conception to early neonatal stage

Mutat Res Rev Mutat Res. 2020 Jan-Mar:783:108295. doi: 10.1016/j.mrrev.2019.108295. Epub 2019 Dec 26.

Abstract

Increasing evidence suggests that early-life events can predispose the newborn to a variety of health issues in later life. In adverse pre- and perinatal conditions, oxidative stress appears to play an important role in the development of future pathological outcomes. From a molecular point of view, oxidative stress can result in genome damage and changes in DNA methylation that can in turn prime pathogenic mechanisms. Interestingly, both alterations have been related to a reciprocal regulation of oxidative stress. The aim of this review is to give a brief overview of the complex relationship linking oxidative stress to DNA damage and methylation and to go through the different sources of exposure that a neonate can encounter in utero or shortly after birth. In this context, the setup of methodologies to monitor the extent of oxidative stress, genomic damage and instability or the presence of altered methylation patterns contributes to the understanding on how the complex events occurring in early life can lead to either a healthy status or a pathological condition.

Keywords: DNA methylation; Genome damage; Mothers; Newborns; Oxidative stress.

Publication types

  • Review

MeSH terms

  • DNA Damage*
  • DNA Methylation*
  • Environmental Exposure / adverse effects
  • Epigenesis, Genetic
  • Female
  • Humans
  • Infant, Newborn
  • Metabolic Diseases / genetics
  • Metabolic Diseases / metabolism
  • Oxidative Stress*
  • Pregnancy
  • Pregnancy Complications / genetics
  • Pregnancy Complications / metabolism
  • Premature Birth