Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases

被引:6332
作者
Verbanck, Marie [1 ,2 ,3 ]
Chen, Chia-Yen [4 ,5 ,6 ]
Neale, Benjamin [4 ,5 ,6 ]
Do, Ron [1 ,2 ,3 ]
机构
[1] Icahn Sch Med Mt Sinai, Charles Bronfman Inst Personalized Med, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Icahn Inst Genom & Multiscale Biol, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[4] Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Boston, MA 02114 USA
[5] Broad Inst, Program Med & Populat Genet, Cambridge, MA USA
[6] Broad Inst, Stanley Ctr Psychiat Res, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
GENOME-WIDE ASSOCIATION; BLOOD-PRESSURE; CARDIOVASCULAR-DISEASE; GENETIC EPIDEMIOLOGY; VARIANTS; COMMON; RISK; INSIGHTS; LOCI;
D O I
10.1038/s41588-018-0099-7
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Horizontal pleiotropy occurs when the variant has an effect on disease outside of its effect on the exposure in Mendelian randomization (MR). Violation of the 'no horizontal pleiotropy' assumption can cause severe bias in MR. We developed the Mendelian randomization pleiotropy residual sum and outlier (MR-PRESSO) test to identify horizontal pleiotropic outliers in multi-instrument summary-level MR testing. We showed using simulations that the MR-PRESSO test is best suited when horizontal pleiotropy occurs in <50% of instruments. Next we applied the MR-PRESSO test, along with several other MR tests, to complex traits and diseases and found that horizontal pleiotropy (i) was detectable in over 48% of significant causal relationships in MR; (ii) introduced distortions in the causal estimates in MR that ranged on average from -131% to 201%; (iii) induced false-positive causal relationships in up to 10% of relationships; and (iv) could be corrected in some but not all instances.
引用
收藏
页码:693 / +
页数:8
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