Polygenic risk for depression and anterior and posterior hippocampal volume in children and adolescents

  • Hailee Hurtado
  • , Melissa Hansen
  • , Jordan Strack
  • , Uku Vainik
  • , Alexandra L. Decker
  • , Budhachandra Khundrakpam
  • , Katherine Duncan
  • , Amy S. Finn
  • , Donald J. Mabbott
  • , Emily C. Merz

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Depression has frequently been associated with smaller hippocampal volume. The hippocampus varies in function along its anterior-posterior axis, with the anterior hippocampus more strongly associated with stress and emotion processing. The goals of this study were to examine the associations among parental history of anxiety/depression, polygenic risk scores for depression (PGS-DEP), and anterior and posterior hippocampal volumes in children and adolescents. To examine specificity to PGS-DEP, we examined associations of educational attainment polygenic scores (PGS-EA) with anterior and posterior hippocampal volume. Methods: Participants were 350 3- to 21-year-olds (46 % female). PGS-DEP and PGS-EA were computed based on recent, large-scale genome-wide association studies. High-resolution, T1-weighted magnetic resonance imaging (MRI) data were acquired, and a semi-automated approach was used to segment the hippocampus into anterior and posterior subregions. Results: Children and adolescents with higher polygenic risk for depression were more likely to have a parent with a history of anxiety/depression. Higher polygenic risk for depression was significantly associated with smaller anterior but not posterior hippocampal volume. PGS-EA was not associated with anterior or posterior hippocampal volumes. Limitations: Participants in these analyses were all of European ancestry. Conclusions: Polygenic risk for depression may lead to smaller anterior but not posterior hippocampal volume in children and adolescents, and there may be specificity of these effects to PGS-DEP rather than PGS-EA. These findings may inform the earlier identification of those in need of support and the design of more effective, personalized treatment strategies. Declarations of interest: none. Declarations of interest: None.

Original languageEnglish
Pages (from-to)619-627
Number of pages9
JournalJournal of affective disorders
Volume344
DOIs
StatePublished - Jan 1 2024

Keywords

  • Brain structure
  • Depression
  • Genetics
  • hippocampus

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