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

Fumihiko TakeuchiMasato AkiyamaNana MatobaTomohiro KatsuyaMasahiro NakatochiYasuharu TabaraAkira NaritaWoei-Yuh SawSanghoon MoonCassandra N SpracklenJin-Fang ChaiYoung-Jin KimLiang ZhangChaolong WangHuaixing LiHonglan LiJer-Yuarn WuRajkumar DorajooJovia L NierenbergYa-Xing WangJing HeDerrick A BennettAtsushi TakahashiYukihide MomozawaMakoto HirataKoichi MatsudaHiromi RakugiEitaro NakashimaMasato IsonoMatsuyuki ShirotaAtsushi HozawaSahoko IchiharaTatsuaki MatsubaraKen YamamotoKatsuhiko KoharaMichiya IgaseSohee HanPenny Gordon-LarsenWei HuangNanette R LeeLinda S AdairMi Yeong HwangJuyoung LeeMiao Li CheeSabanayagam CharumathiWanting ZhaoJian-Jun LiuDermot F ReillyLiang SunShaofeng HuoTodd L EdwardsJirong LongLi-Ching ChangChien-Hsiun ChenJian-Min YuanWoon-Puay KohYechiel FriedlanderTanika N KellyWen Bin WeiLiang XuHui CaiYong-Bing XiangKuang LinRobert ClarkeRobin G WaltersIona Y MillwoodLiming LiJohn C ChambersJaspal S KoonerPaul ElliottPim van der Harstnull nullZhengming ChenMakoto SasakiXiao-Ou ShuJost Bruno JonasJiang HeChew-Kiat HengYuan-Tsong ChenQuan LongXu LinYik-Ying TeoE-Shyong TaiChing-Yu ChengTien Yin WongXueling S SimKaren L MohlkeMasayuki YamamotoBong-Jo KimTetsuro MikiToru NabikaMitsuhiro YokotaYoichiro KamataniMichiaki KuboNorihiro Kato
Published in: Nature communications (2018)
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 Nā€‰=ā€‰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.
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