LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

被引:3073
作者
Bulik-Sullivan, Brendan K. [1 ,2 ,3 ,4 ]
Loh, Po-Ru [1 ,5 ]
Finucane, Hilary K. [5 ,6 ]
Ripke, Stephan [2 ,3 ,4 ]
Yang, Jian [7 ]
Patterson, Nick [1 ]
Daly, Mark J. [1 ,2 ,3 ,4 ]
Price, Alkes L. [1 ,5 ,8 ]
Neale, Benjamin M. [1 ,2 ,3 ,4 ]
机构
[1] Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA
[2] Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA USA
[5] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[6] MIT, Dept Math, Cambridge, MA 02139 USA
[7] Univ Queensland, Queensland Brain Inst, Brisbane, Qld, Australia
[8] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
GENETIC ARCHITECTURE; IDENTIFIES; 13; METAANALYSIS; LOCI; LINKAGE; TRAITS; MODELS; REGIONS; RISK;
D O I
10.1038/ng.3211
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Both polygenicity (many small genetic effects) and confounding biases, such as cryptic relatedness and population stratification, can yield an inflated distribution of test statistics in genome-wide association studies (GWAS). However, current methods cannot distinguish between inflation from a true polygenic signal and bias. We have developed an approach, LD Score regression, that quantifies the contribution of each by examining the relationship between test statistics and linkage disequilibrium (LD). The LD Score regression intercept can be used to estimate a more powerful and accurate correction factor than genomic control. We find strong evidence that polygenicity accounts for the majority of the inflation in test statistics in many GWAS of large sample size.
引用
收藏
页码:291 / +
页数:7
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