Turecki Gustavo, Meaney Michael J
Douglas Mental Health University Institute, McGill Group for Suicide Studies, and Ludmer Centre for Neuroinformatics and Mental Health, Department of Psychiatry, McGill University, Montreal, Canada.
Douglas Mental Health University Institute, McGill Group for Suicide Studies, and Ludmer Centre for Neuroinformatics and Mental Health, Department of Psychiatry, McGill University, Montreal, Canada.
Biol Psychiatry. 2016 Jan 15;79(2):87-96. doi: 10.1016/j.biopsych.2014.11.022. Epub 2014 Dec 13.
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 17 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 1F in humans or the GR17 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 1F/17 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 17 methylation and 17% of human studies reporting increased exon 1F 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.
早期生活的社会环境可引发影响神经发育和心理健康的稳定变化。聚焦于早期生活逆境的研究表明,早期生活经历通过表观遗传机制对基因表达和行为产生持久影响。下丘脑 - 垂体 - 肾上腺轴对早期生活环境的变化敏感,这些变化与糖皮质激素受体(GR)(Nr3c1)的神经元特异性外显子17启动子的DNA甲基化有关。自2004年首次发表相关研究结果以来,众多报告对GR基因甲基化与早期生活经历、父母压力和精神病理学之间的关系进行了调查。我们对这一不断增长的文献进行了系统综述,确定了自2004年以来发表的40篇文章(13篇动物研究和27篇人类研究)。其中大多数研究了人类的GR外显子变体1F或大鼠的GR17,89%的人类早期生活逆境研究和70%的动物研究报告该外显子变体的甲基化增加。所有在父母压力条件下研究外显子1F/17甲基化的研究(一项动物研究和七项人类研究)也报告甲基化增加。研究心理社会压力和精神病理学的结果不太一致,67%的动物研究报告外显子17甲基化增加,17%的人类研究报告外显子1F甲基化增加。我们发现,即使不同研究中社会环境逆境的确切表型和测量方法有所不同,但在研究早期生活逆境和父母压力影响的研究之间仍具有高度一致性。这些结果令人鼓舞,值得进一步研究,以更好地理解这些关联的相关性和特征。