Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent

被引:76
|
作者
de Candia, Teresa R. [1 ,2 ]
Lee, S. Hong [3 ]
Yang, Jian [3 ,4 ]
Browning, Brian L. [5 ]
Gejman, Pablo V. [6 ,7 ]
Levinson, Douglas F. [8 ]
Mowry, Bryan J. [3 ,9 ]
Hewitt, John K. [1 ,2 ]
Goddard, Michael E. [10 ,11 ]
O'Donovan, Michael C. [12 ]
Purcell, Shaun M. [13 ]
Posthuma, Danielle [14 ,15 ,16 ]
Visscher, Peter M. [3 ,4 ]
Wray, Naomi R. [3 ]
Keller, Matthew C. [1 ,2 ]
机构
[1] Univ Colorado, Dept Psychol & Neurosci, Boulder, CO 80302 USA
[2] Univ Colorado, Inst Behav Genet, Boulder, CO 80302 USA
[3] Univ Queensland, Queensland Brain Inst, Brisbane, Qld 4072, Australia
[4] Univ Queensland, Diamantina Inst, Brisbane, Qld 4072, Australia
[5] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98195 USA
[6] Northshore Univ Hlth Syst, Dept Psychiat & Behav Sci, Evanston, IL 60601 USA
[7] Univ Chicago, Evanston, IL 60601 USA
[8] Stanford Univ, Dept Psychiat & Behav Sci, Palo Alto, CA 94305 USA
[9] Queensland Ctr Mental Hlth Res, Brisbane, Qld 4076, Australia
[10] Univ Melbourne, Dept Agr & Food Syst, Melbourne, Vic 3010, Australia
[11] Dept Primary Ind, Biosci Res Div, Melbourne, Vic 3001, Australia
[12] Cardiff Univ, Sch Med, MRC Ctr Neuropsychiat Genet & Genom, Cardiff CF14 4XN, S Glam, Wales
[13] Broad Inst, Cambridge, MA 02141 USA
[14] Vrije Univ Amsterdam, Ctr Neurogen & Cognit Res, Dept Funct Genom, NL-1081 HV Amsterdam, Netherlands
[15] Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, NL-1081 HV Amsterdam, Netherlands
[16] Erasmus Univ, Sophia Child Hosp, Dept Child & Adolescent Psychiat, NL-3000 CB Rotterdam, Netherlands
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
LINKAGE DISEQUILIBRIUM; COMMON; VARIANTS; GENOMICS; ASSOCIATION; SNPS; TWIN;
D O I
10.1016/j.ajhg.2013.07.007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To investigate the extent to which the proportion of schizophrenia's additive genetic variation tagged by SNPs is shared by populations of European and African descent, we analyzed the largest combined African descent (AD [n = 2,142]) and European descent (ED [n = 4,990]) schizophrenia case-control genome-wide association study (GWAS) data set available, the Molecular Genetics of Schizophrenia (MGS) data set. We show how a method that uses genomic similarities at measured SNPs to estimate the additive genetic correlation (SNP correlation [SNP-r(g)]) between traits can be extended to estimate SNP-r(g) for the same trait between ethnicities. We estimated SNP-r(g) for schizophrenia between the MGS ED and MGS AD samples to be 0.66 (SE = 0.23), which is significantly different from 0 (P(SNP-rg (= 0)) = 0.0003), but not 1 (p((SNP-rg = 1)) = 0.26). We re-estimated SNP-r(g) between an independent ED data set (n = 6,665) and the MGS AD sample to be 0.61 (SE = 0.21, P(SNP-rg = 0) = 0.0003, p((SNP-rg = 1)) = 0.16). These results suggest that many schizophrenia risk alleles are shared across ethnic groups and predate African-European divergence.
引用
收藏
页码:463 / 470
页数:8
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