University of Leicester
Browse
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.pdf (1.9 MB)

Interethnic analyses of blood pressure loci in populations of East Asian and European descent.

Download (1.9 MB)
journal contribution
posted on 2019-08-15, 11:41 authored by F Takeuchi, M Akiyama, N Matoba, T Katsuya, M Nakatochi, Y Tabara, A Narita, W-Y Saw, S Moon, CN Spracklen, J-F Chai, Y-J Kim, L Zhang, C Wang, H Li, J-Y Wu, R Dorajoo, JL Nierenberg, YX Wang, J He, DA Bennett, A Takahashi, Y Momozawa, M Hirata, K Matsuda, H Rakugi, E Nakashima, M Isono, M Shirota, A Hozawa, S Ichihara, T Matsubara, K Yamamoto, K Kohara, M Igase, S Han, P Gordon-Larsen, W Huang, NR Lee, LS Adair, MY Hwang, J Lee, ML Chee, C Sabanayagam, W Zhao, J Liu, DF Reilly, L Sun, S Huo, TL Edwards, J Long, L-C Chang, C-H Chen, J-M Yuan, W-P Koh, Y Friedlander, TN Kelly, W Bin Wei, L Xu, H Cai, Y-B Xiang, K Lin, R Clarke, RG Walters, IY Millwood, L Li, JC Chambers, JS Kooner, P Elliott, P van der Harst, International Genomics of Blood Pressure (iGEN-BP) Consortium, Z Chen, M Sasaki, X-O Shu, JB Jonas, C-K Heng, Y-T Chen, W Zheng, X Lin, Y-Y Teo, E-S Tai, C-Y Cheng, TY Wong, X Sim, KL Mohlke, M Yamamoto, B-J Kim, T Miki, T Nabika, M Yokota, Y Kamatani, M Kubo, N Kato
Blood pressure (BP) is a major risk factor for cardiovascular disease and more than 200 genetic loci associated with BP are known. Here, we perform a multi-stage genome-wide association study for BP (max N = 289,038) principally in East Asians and meta-analysis in East Asians and Europeans. We report 19 new genetic loci and ancestry-specific BP variants, conforming to a common ancestry-specific variant association model. At 10 unique loci, distinct non-rare ancestry-specific variants colocalize within the same linkage disequilibrium block despite the significantly discordant effects for the proxy shared variants between the ethnic groups. The genome-wide transethnic correlation of causal-variant effect-sizes is 0.898 and 0.851 for systolic and diastolic BP, respectively. Some of the ancestry-specific association signals are also influenced by a selective sweep. Our results provide new evidence for the role of common ancestry-specific variants and natural selection in ethnic differences in complex traits such as BP.

Funding

We acknowledge the use of data from the International Consortium for Blood Pressure Genome-Wide Association Studies 3 and the AGEN-height Consortium 42. This research has been conducted using the UK Biobank Resource 14. Additional acknowledgements can be found in Supplementary Note 1.

History

Citation

Nature Communications, 2018, 9:5052

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Department of Cardiovascular Sciences

Version

  • VoR (Version of Record)

Published in

Nature Communications

Publisher

Nature Research (part of Springer Nature)

eissn

2041-1723

Acceptance date

2018-10-29

Copyright date

2018

Available date

2019-08-15

Publisher version

https://www.nature.com/articles/s41467-018-07345-0

Notes

Supplementary Information accompanies this paper at https://doi.org/10.1038/s41467-018-07345-0 Full summary statistics relating to the GWAS meta-analysis has been deposited at the European Genome-phenome Archive (EGA), which is hosted by the EBI and the CRG, under accession number EGAS00001002991. Further information about EGA can be found on https://ega-archive.org “The European Genome-phenome Archive of human data consented for biomedical research” (http://www.nature.com/ng/journal/v47/n7/full/ng.3312.html). All relevant data are available from the authors.

Language

en