Glucocorticoid receptor gene (NR3C1) methylation processes as mediators of early adversity in stress-related disorders causality: A critical review

被引:243
|
作者
Palma-Gudiel, Helena [1 ]
Cordova-Palomera, Aldo [1 ,2 ]
Carlos Leza, Juan [2 ,3 ]
Fananas, Lourdes [1 ,2 ]
机构
[1] Univ Barcelona, Fac Biol, Dept Anim Biol, Unity Anthropol,Inst Biomed IBUB, E-08028 Barcelona, Spain
[2] Ctr Invest Biomed Red Salud Mental CIBERSAM, Madrid 28007, Spain
[3] Univ Complutense, Fac Med, Dept Pharmacol, E-28040 Madrid, Spain
关键词
DNA methylation; NR3C1; gene; Glucocorticoid receptor; Early life stress; Stress-related disorders; DNA METHYLATION; CHILDHOOD MALTREATMENT; EPIGENETIC REGULATION; IN-UTERO; DEPRESSION; EXPRESSION; EXPOSURE; BRAIN; IDENTIFICATION; EPIDEMIOLOGY;
D O I
10.1016/j.neubiorev.2015.05.016
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Early life stress (ELS) is a known risk factor for suffering psychopathology in adulthood. The hypothalamic-pituitary-adrenal (HPA) axis has been described to be deregulated in both individuals who experienced early psychosocial stress and in patients with a wide range of psychiatric disorders. The NR3C1 gene codes for the glucocorticoid receptor, a key element involved in several steps of HPA axis modulation. In this review, we gather existing evidence linking NR3C1 methylation pattern with either ELS or psychopathology. We summarize that several types of ELS have been frequently associated with NR3C1 hypermethylation whereas hypomethylation has been continuously found to be associated with post-traumatic stress disorder. In light of the reported findings, the main concerns of ongoing research in this field are the lack of methodological consensus and selection of CpG sites. Further studies should target individual CpG site methylation assessment focusing in biologically relevant areas such as transcription factor binding regions whereas widening the examined sequence in order to include all non-coding first exons of the NR3C1 gene in the analysis. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:520 / 535
页数:16
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