| Literature DB >> 29039414 |
Ronny Redlich1, Nils Opel1, Christian Bürger1, Katharina Dohm1, Dominik Grotegerd1, Katharina Förster1, Dario Zaremba1, Susanne Meinert1, Jonathan Repple1, Verena Enneking1, Elisabeth Leehr1, Joscha Böhnlein1, Lena Winters1, Neele Froböse1, Sophia Thrun1, Julia Emtmann1, Walter Heindel2, Harald Kugel2, Volker Arolt1, Georg Romer3, Christian Postert3,4, Udo Dannlowski1.
Abstract
Adolescent-onset major depressive disorder (MDD) is associated with an increased risk of recurrent depressive episodes, suicidal behaviors, and psychiatric morbidity throughout the lifespan. The objective of the present study was to investigate brain structural and functional changes in adolescent patients with MDD. Furthermore, we aimed to clarify the influence of early-life stress on brain function and structure. The study investigated adolescent patients with severe MDD (n=20, mean age=16.0, range=15-18 years) and a control sample of matched healthy adolescents (n=21, mean age=16.6, range=15-18 years). Functional MRI data were obtained using a face-matching paradigm to investigate emotion processing. Structural MRI data were analyzed using voxel-based morphometry (VBM). In line with previous studies on adult MDD, adolescent patients showed elevated amygdala activity to negative and reduced amygdala activity to positive emotional stimuli. Furthermore, MDD patients showed smaller hippocampal volumes compared to healthy adolescents. Higher levels of childhood maltreatment were associated with smaller hippocampal volumes in both depressed patients and healthy controls, whereby no associations between amygdala reactivity and childhood maltreatment were found. Our results suggest that hippocampal alterations in youth MDD patients may at least partly be traced back to higher occurrence of early-life adverse experiences. Regarding the strong morphometric impact of childhood maltreatment and its distinctly elevated prevalence in MDD populations, this study provides an alternative explanation for frequently observed limbic structural abnormalities in depressed patients.Entities:
Mesh:
Year: 2017 PMID: 29039414 PMCID: PMC5770774 DOI: 10.1038/npp.2017.246
Source DB: PubMed Journal: Neuropsychopharmacology ISSN: 0893-133X Impact factor: 7.853