Citation

Normann C, Buttenschøn HN. Acta Neuropsyciatr. 2020; ePub(ePub): ePub.

Affiliation

NIDO Denmark, Regional Hospital West Jutland, Denmark.

Copyright

(Copyright © 2020, Cambridge University Press)

DOI

10.1017/neu.2020.1

PMID

31902387

Abstract

OBJECTIVE: Gene-Environment (GxE) interactions may comprise an important part of the aetiology of depression, and childhood maltreatment, a significant stressor, has consistently been linked to depression. Hence, in this systematic review, we aimed to investigate the interaction between hypothalamus-pituitary-adrenal axis (HPA-axis) genes and childhood maltreatment (CM) in depression.

METHODS: We conducted a literature search using the Pubmed, Embase, and PsychINFO databases in adherence with the PRISMA guidelines. We included studies investigating GxE interactions between HPA-axis genes (Angiotensin Converting Enzyme (ACE), Arginine Vasopressin (AVP), Corticotrophin Releasing Hormone (CRH), Corticotrophin Releasing Hormone Receptor 1 (CRHR1), Corticotrophin Releasing Hormone Receptor 2 (CRHR2), FK506 binding protein (FKBP5), Nuclear Receptor subfamily 3 group C member 1 (NR3C1), Nuclear Receptor subfamily 3 group C member 2 (NR3C2) and CM in depression.

RESULTS: The literature search identified 159 potentially relevant studies. Following screening, 138 of these were excluded. Thus, 21 studies, investigating a total of 51 single nucleotide polymorphisms (SNPs), were included in the final study. The most prevalent genes in the current study were CRHR1 and FKBP5. Significant GxE interactions were reported in seven of eight studies for CRHR1:rs110402 and CM, and in five of eight studies for FKBP5:rs1360780 and CM. In summary, our results suggest possible GxE interactions between CRHR1, FKBP5, NR3C1, and NR3C2 and CM, respectively. For the remaining genes, no relevant literature emerged.

CONCLUSIONS: We find that genetic variation in four HPA-axis genes may influence the effects of CM in depression.

Language: en

Keywords

Adult Survivors of Child Adverse Events; Depression; Gene-Environment Interaction; Life Change Events; Single Nucleotide Polymorphism