Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Evidence for association between familial bipolar risk and ventral striatal volume

Lancaster, Thomas 2018. Evidence for association between familial bipolar risk and ventral striatal volume. Journal of Affective Disorders 232 , pp. 69-72. 10.1016/j.jad.2018.02.015

[img]
Preview
PDF - Published Version
Available under License Creative Commons Attribution.

Download (275kB) | Preview

Abstract

Background: Recent genome-wide association studies (GWAS) of striatal volumes and bipolar disorder (BD) indicate these traits are heritable and share common genetic architecture, however little independent work has been conducted to help establish this relationship. Methods: Subcortical volumes (mm3) of young, healthy offspring of BD (N= 32) and major depressive disorder (MDD) patients (N= 158) were compared to larger healthy control sample (NRANGE=925–1052) adjusting for potential confounds, using data from the latest release (S1200) of the Human Connectome Project. Based on recent GWAS findings, it was hypothesised that the accumbens and caudate would be smaller in offspring of BD, but not MDD patients. Results: After multiple comparison correction, there was a regional and BD specific relationship in the direction expected (Accumbens: F2,1067=6.244, PFDR-CORRECTED=0.014). Discussion: In line with recent GWAS, there was evidence supporting the hypothesis that reduced striatal volume may be part of the genetic risk for BD, but not MDD. Limitations: It cannot be concluded whether this association was specific to BD or consistent with a broader psychosis phenotype, due to a small sample size for offspring of schizophrenia patients. Furthermore, one cannot rule out potential shared environmental influences of parental BD. Conclusions: The common genetic architecture of BD may confer susceptibility via inherited genetic factors that affect striatal volume. Future work should establish how this relationship relates to specific BD symptomology. This work may also help to dissect clinical heterogeneity and improve diagnosis nosology.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Cardiff University Brain Research Imaging Centre (CUBRIC)
Medicine
Neuroscience and Mental Health Research Institute (NMHRI)
Publisher: Elsevier
ISSN: 0165-0327
Date of First Compliant Deposit: 23 March 2018
Date of Acceptance: 15 February 2018
Last Modified: 15 Apr 2019 08:47
URI: http://orca.cf.ac.uk/id/eprint/110148

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics