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Journal Article

Citation

Buttenschøn HN, Krogh J, Nielsen MN, Kaerlev L, Nordentoft M, Mors O. Acta Neuropsyciatr. 2017; 29(1): 59-64.

Copyright

(Copyright © 2017, Cambridge University Press)

DOI

10.1017/neu.2016.26

PMID

unavailable

Abstract

OBJECTIVE
Dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis has been reported in depression. The aim was to investigate the potential association between depression and seven genes regulating or interfering with the HPA axis, including the gene encoding angiotensin converting enzyme (ACE).


Methods
In total, 78 single nucleotide polymorphisms (SNPs) and one insertion/deletion polymorphism were genotyped. The study included 408 individuals with depression and 289 controls. In a subset of cases, the interaction between genetic variants and stressful life events (SLEs) was investigated.


Results
After quality control, 68 genetic variants were left for analyses. Four of nine variants within ACE were nominally associated with depression and a gene-wise association was likewise observed. However, none of the SNPs located within AVP, CRH, CRHR1, CRHR2, FKBP5 or NC3C1 were associated with depression. One nominally significant interaction, most likely due to chance, was identified.


Conclusion
The results indicate that ACE could be a potential candidate gene for depression.


Language: en

Keywords

angiotensin converting enzyme (ACE); association; depression; hypothalamus–pituitary–adrenal (HPA) axis; single nucleotide polymorphism (SNP)

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