| Literature DB >> 30010813 |
Bingxin Zhao1, Joseph G Ibrahim1,2, Yun Li1,3,4, Tengfei Li5, Yue Wang1, Yue Shan1, Ziliang Zhu1, Fan Zhou1, Jingwen Zhang1, Chao Huang1, Huiling Liao6, Liuqing Yang2, Paul M Thompson7, Hongtu Zhu1,5.
Abstract
Brain genetics is an active research area. The degree to which genetic variants impact variations in brain structure and function remains largely unknown. We examined the heritability of regional brain volumes (P ~ 100) captured by single-nucleotide polymorphisms (SNPs) in UK Biobank (n ~ 9000). We found that regional brain volumes are highly heritable in this study population and common genetic variants can explain up to 80% of their variabilities (median heritability 34.8%). We observed omnigenic impact across the genome and examined the enrichment of SNPs in active chromatin regions. Principal components derived from regional volume data are also highly heritable, but the amount of variance in brain volume explained by the component did not seem to be related to its heritability. Heritability estimates vary substantially across large-scale functional networks, exhibit a symmetric pattern across left and right hemispheres, and are consistent in females and males (correlation = 0.638). We repeated the main analysis in Alzheimer's Disease Neuroimaging Initiative (n ~ 1100), Philadelphia Neurodevelopmental Cohort (n ~ 600), and Pediatric Imaging, Neurocognition, and Genetics (n ~ 500) datasets, which demonstrated that more stable estimates can be obtained from the UK Biobank.Entities:
Keywords: SNP heritability; UK Biobank; regional brain volumes
Mesh:
Year: 2019 PMID: 30010813 PMCID: PMC6611460 DOI: 10.1093/cercor/bhy157
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 5.357