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

• Published in: Journal of affective disorders Vol. 252; pp. 152 - 159
• Main Authors: Mikolas, Pavol, Tozzi, Leonardo, Doolin, Kelly, Farrell, Chloe, O'Keane, Veronica, Frodl, Thomas
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.06.2019
• Subjects: Adult; Amygdala - pathology; Dentate Gyrus - pathology; Depressive Disorder, Major - genetics; Depressive Disorder, Major - pathology; Early life adversity; Female; FKBP5; Genotype; Hippocampal subfields; Hippocampus; Hippocampus - pathology; Humans; Magnetic Resonance Imaging; Major depression; Male; Middle Aged; Neuronal Plasticity - genetics; Organ Size; rs1360780; Stress, Psychological - genetics; Tacrolimus Binding Proteins - genetics; Temporal Lobe - pathology; Early life adversity; Hippocampal subfields; rs1360780; Major depression; Hippocampus; FKBP5
• ISSN: 0165-0327; 1573-2517; 1573-2517
• DOI: 10.1016/j.jad.2019.04.054

•MDD patients had smaller volumes within the cornu ammonis and dentate gyrus.•MDD exposed to early life adversity had larger hippocampi and their subfields.•There was an interaction of FKBP5 and early life adversity in the HATA subfield. 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. 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. 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 hippocampus-amygdala-transition-area (HATA) as those subjects homozygous for the C allele. We pooled the subjects from 2 centers in order to increase the sample size. We did not include the cumulative lifetime exposure to medication. 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.