4.7 Article

Effects of early life adversity and FKBP5 genotype on hippocampal subfields volume in major depression

Journal

JOURNAL OF AFFECTIVE DISORDERS
Volume 252, Issue -, Pages 152-159

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jad.2019.04.054

Keywords

FKBP5; Early life adversity; Hippocampus; Hippocampal subfields; Major depression; rs1360780

Funding

  1. Science Foundation Ireland
  2. Health Research Board
  3. SFI Science Foundation Ireland
  4. Stokes Professorship grant [S.F.I. 07/SK/B1214C-Frodl]

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Background: Smaller hippocampus volume represents a consistent finding in major depression (MDD). Hippocampal neuroplasticity due to chronic stress might have differential effect on hippocampal subfields. We investigated the effects of the rs1360780 polymorphism of the hypothalamic-pituitary-axis related gene FKBP5 in combination with early life stress (ELA) on the structure of hippocampal subfields in MDD. Methods: We assessed the hippocampal subfields volumes in 85/67 MDD/healthy controls. We investigated the effects of diagnosis, FKBP5 allelic status and their interaction as predictors of hippocampal subfield volumes as well as the effect of ELA and its interaction with FKBP5. Results: MDD patients had smaller hippocampal volumes, in particular within the cornu ammonis (CA) and dentate gyrus (DG) regions. Patients exposed to ELA had larger hippocampi, in particular within the CA and DG. Among the patients exposed to ELA, the T allele carriers displayed lower volumes within the hippocampusamygdala-transition-area (HATA) as those subjects homozygous for the C allele. Limitations: We pooled the subjects from 2 centers in order to increase the sample size. We did not include the cumulative lifetime exposure to medication. Conclusions: Hippocampal volume reductions in MDD were present particularly in the CA and DG. MDD with ELA display differential volume changes compared to MDD without ELA. The significant interaction between ELA and the rs1360780 polymorphism in HATA suggests a role of FKBP5 in the pathophysiology of structural alterations in depression.

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