학술논문

The genetic architecture of human amygdala volumes and their overlap with common brain disorders
Document Type
article
Source
Translational Psychiatry, Vol 13, Iss 1, Pp 1-12 (2023)
Subject
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Language
English
ISSN
2158-3188
Abstract
Abstract The amygdala is a crucial interconnecting structure in the brain that performs several regulatory functions, yet its genetic architectures and involvement in brain disorders remain largely unknown. We carried out the first multivariate genome-wide association study (GWAS) of amygdala subfield volumes in 27,866 UK Biobank individuals. The whole amygdala was segmented into nine nuclei groups using Bayesian amygdala segmentation. The post-GWAS analysis allowed us to identify causal genetic variants in phenotypes at the SNP, locus, and gene levels, as well as genetic overlap with brain health-related traits. We further generalized our GWAS in Adolescent Brain Cognitive Development (ABCD) cohort. The multivariate GWAS identified 98 independent significant variants within 32 genomic loci associated (P