4.7 Review

Effects of the Social Environment and Stress on Glucocorticoid Receptor Gene Methylation: A Systematic Review

Journal

BIOLOGICAL PSYCHIATRY
Volume 79, Issue 2, Pages 87-96

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2014.11.022

Keywords

DNA methylation; Early-life adversity; Epigenetics; Glucocorticoid receptor; Social environment; Systematic review

Funding

  1. Canadian Institute of Health Research [MOP93775, MOP11260, MOP119429, MOP119430]
  2. National Institutes of Health [1R01DA033684-01]
  3. Fonds de Recherche du Quebec - Sante' through a Chercheur National Salary Award
  4. Quebec Network on Suicide, Mood Disorders, and Related Disorders

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The early-life social environment can induce stable changes that influence neurodevelopment and mental health. Research focused on early-life adversity revealed that early-life experiences have a persistent impact on gene expression and behavior through epigenetic mechanisms. The hypothalamus-pituitary-adrenal axis is sensitive to changes in the early-life environment that associate with DNA methylation of a neuron-specific exon 1(7) promoter of the glucocorticoid receptor (GR) (Nr3c1). Since initial findings were published in 2004, numerous reports have investigated GR gene methylation in relationship to early-life experience, parental stress, and psychopathology. We conducted a systematic review of this growing literature, which identified 40 articles (13 animal and 27 human studies) published since 2004. The majority of these examined the GR exon variant 1(F) in humans or the GR1(7) in rats, and 89% of human studies and 70% of animal studies of early-life adversity reported increased methylation at this exon variant. All the studies investigating exon 1(F)/1(7) methylation in conditions of parental stress (one animal study and seven human studies) also reported increased methylation. Studies examining psychosocial stress and psychopathology had less consistent results, with 67% of animal studies reporting increased exon 1(7) methylation and 17% of human studies reporting increased exon 1(F) methylation. We found great consistency among studies investigating early-life adversity and the effect of parental stress, even if the precise phenotype and measures of social environment adversity varied among studies. These results are encouraging and warrant further investigation to better understand correlates and characteristics of these associations.

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