RT Journal Article
SR Electronic
T1 Do Regional Brain Volumes and Major Depressive Disorder Share Genetic Architecture: A Study in Generation Scotland (n=19,762), UK Biobank (n=24,048) and the English Longitudinal Study of Ageing (n=5,766)
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 059352
DO 10.1101/059352
A1 Eleanor M. Wigmore
A1 Toni-Kim Clarke
A1 Mark J. Adams
A1 Ana M. Fernandez-Pujals
A1 Jude Gibson
A1 Gail Davies
A1 Lynsey S. Hall
A1 Yanni Zeng
A1 Pippa A. Thomson
A1 Caroline Hayward
A1 Blair H. Smith
A1 Lynne J. Hocking
A1 Sandosh Padmanabhan
A1 Ian J. Deary
A1 David J. Porteous
A1 Jude Gibson
A1 Kristin K. Nicodemus
A1 Andrew M. McIntosh
YR 2016
UL http://biorxiv.org/content/early/2016/06/20/059352.abstract
AB Major depressive disorder (MDD) is a highly debilitating and heritable disorder. It is commonly associated with subcortical volumetric abnormalities, the most replicated of these being reduced hippocampal volume. Using the most recent published data from ENIGMA consortium’s genome-wide association study (GWAS) of regional brain volume, we sought to test whether there is shared genetic architecture between subcortical brain volumes and MDD. Using LD score regression utilising summary statistics from ENIGMA and the Psychiatric Genomics Consortium, we demonstrated that hippocampal volume was genetically correlated with MDD (rG=0.46, P=0.02), although this did not survive multiple comparison testing. None of other six regions were genetically correlated and amygdala volume heritability was too low for analysis. We also generated polygenic risk scores (PRS) to assess potential pleiotropy on regional brain volumes and MDD in three cohorts (Generation Scotland; Scottish Family Health Study (n=19,762), UK Biobank (n=24,048) and the English Longitudinal Study of Ageing (n=5,766)). We used logistic regression to examine volumetric PRS and MDD and performed a meta-analysis across the three cohorts. No regional volumetric PRS demonstrated any significant association with lifetime MDD or recurrent MDD. In this study we provide evidence that hippocampal volume and MDD have a shared genetic architecture providing further evidence of the potential mechanistic importance of the hippocampus in depression. We found no evidence to support a shared genetic architecture for MDD with any other subcortical region.