Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n=17,706)

被引:81
|
作者
Zhao, Bingxin [1 ]
Zhang, Jingwen [1 ]
Ibrahim, Joseph G. [1 ]
Luo, Tianyou [1 ]
Santelli, Rebecca C. [2 ]
Li, Yun [1 ,3 ,4 ]
Li, Tengfei [5 ,6 ]
Shan, Yue [1 ]
Zhu, Ziliang [1 ]
Zhou, Fan [1 ]
Liao, Huiling [7 ]
Nichols, Thomas E. [8 ]
Zhu, Hongtu [1 ,6 ]
机构
[1] Univ N Carolina, Dept Biostat, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Psychiat, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Genet, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Comp Sci, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Dept Radiol, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Biomed Res Imaging Ctr, Sch Med, Chapel Hill, NC 27599 USA
[7] Texas A&M Univ, Dept Stat, College Stn, TX 77843 USA
[8] Univ Oxford, Wellcome Trust Ctr Integrat Neuroimaging, Big Data Inst, Oxford OX1 2JD, England
关键词
GENOME-WIDE ASSOCIATION; COMPLEX TRAITS; FRACTIONAL ANISOTROPY; POLYGENIC RISK; METAANALYSIS REVEALS; SPATIAL STATISTICS; DIFFUSION TENSOR; HERITABILITY; DTI; EXPRESSION;
D O I
10.1038/s41380-019-0569-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Individual variations of white matter (WM) tracts are known to be associated with various cognitive and neuropsychiatric traits. Diffusion tensor imaging (DTI) and genome-wide single-nucleotide polymorphism (SNP) data from 17,706 UK Biobank participants offer the opportunity to identify novel genetic variants of WM tracts and explore the genetic overlap with other brain-related complex traits. We analyzed the genetic architecture of 110 tract-based DTI parameters, carried out genome-wide association studies (GWAS), and performed post-GWAS analyses, including association lookups, gene-based association analysis, functional gene mapping, and genetic correlation estimation. We found that DTI parameters are substantially heritable for all WM tracts (mean heritability 48.7%). We observed a highly polygenic architecture of genetic influence across the genome (p value = 1.67 x 10(-05)) as well as the enrichment of genetic effects for active SNPs annotated by central nervous system cells (p value = 8.95 x 10(-12)). GWAS identified 213 independent significant SNPs associated with 90 DTI parameters (696 SNP-level and 205 locus-level associations; p value < 4.5 x 10(-10), adjusted for testing multiple phenotypes). Gene-based association study prioritized 112 significant genes, most of which are novel. More importantly, association lookups found that many of the novel SNPs and genes of DTI parameters have previously been implicated with cognitive and mental health traits. In conclusion, the present study identifies many new genetic variants at SNP, locus and gene levels for integrity of brain WM tracts and provides the overview of pleiotropy with cognitive and mental health traits.
引用
收藏
页码:3943 / 3955
页数:13
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