Genome-wide association study of medication-use and associated disease in the UK Biobank

被引:166
作者
Wu, Yeda [1 ]
Byrne, Enda M. [1 ]
Zheng, Zhili [1 ,2 ]
Kemper, Kathryn E. [1 ]
Yengo, Loic [1 ]
Mailett, Andrew J. [1 ,3 ]
Yang, Jian [1 ,2 ,4 ]
Visscher, Peter M. [1 ,4 ]
Wray, Naomi R. [1 ,4 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Wenzhou Med Univ, Inst Adv Res, Wenzhou 325027, Zhejiang, Peoples R China
[3] Royal Brisbane & Womens Hosp, Dept Renal Med, Herston, Qld 4029, Australia
[4] Univ Queensland, Queensland Brain Inst, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
BLOOD-PRESSURE; DEPRESSIVE SYMPTOMS; GENETIC-VARIANTS; LOCI; GWAS; INSIGHTS; GHRELIN; PATHOPHYSIOLOGY; ENRICHMENT; DATABASE;
D O I
10.1038/s41467-019-09572-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genome-wide association studies (GWASs) of medication use may contribute to understanding of disease etiology, could generate new leads relevant for drug discovery and can be used to quantify future risk of medication taking. Here, we conduct GWASs of self-reported medication use from 23 medication categories in approximately 320,000 individuals from the UK Biobank. A total of 505 independent genetic loci that meet stringent criteria (P < 10(-8) /23) for statistical significance are identified. We investigate the implications of these GWAS findings in relation to biological mechanism, potential drug target identification and genetic risk stratification of disease. Amongst the medication-associated genes are 16 known therapeutic-effect target genes for medications from 9 categories. Two of the medication classes studied are for disorders that have not previously been subject to large GWAS (hypothyroidism and gastro-oesophageal reflux disease).
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页数:10
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