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Research output: Contribution to Journal/Magazine › Journal article › peer-review
Research output: Contribution to Journal/Magazine › Journal article › peer-review
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TY - JOUR
T1 - Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
AU - Warren, Helen R.
AU - Evangelou, Evangelos
AU - Cabrera, Claudia P.
AU - Gao, He
AU - Ren, Meixia
AU - Mifsud, Borbala
AU - Ntalla, Ioanna
AU - Surendran, Praveen
AU - Liu, Chunyu
AU - Cook, James P.
AU - Kraja, Aldi T.
AU - Drenos, Fotios
AU - Loh, Marie
AU - Verweij, Niek
AU - Marten, Jonathan
AU - Karaman, Ibrahim
AU - Lepe, Marcelo P. Segura
AU - O'Reilly, Paul F.
AU - Knight, Joanne
AU - Snieder, Harold
AU - Kato, Norihiro
AU - He, Jiang
AU - Tai, E. Shyong
AU - Said, M. Abdullah
AU - Porteous, David
AU - Alver, Maris
AU - Poulter, Neil
AU - Farrall, Martin
AU - Gansevoort, Ron T.
AU - Padmanabhan, Sandosh
AU - Mägi, Reedik
AU - Stanton, Alice
AU - Connell, John
AU - Bakker, Stephan J. L.
AU - Metspalu, Andres
AU - Shields, Denis C.
AU - Thom, Simon
AU - Brown, Morris
AU - Sever, Peter
AU - Esko, Tõnu
AU - Hayward, Caroline
AU - van der Harst, Pim
AU - Saleheen, Danish
AU - Chowdhury, Rajiv
AU - Chambers, John C.
AU - Chasman, Daniel I.
AU - Chakravarti, Aravinda
AU - Newton-Cheh, Christopher
AU - Lindgren, Cecilia M.
AU - Levy, Daniel
AU - International Consortium of Blood Pressure (ICBP) 1000G Analyses
N1 - © 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.
PY - 2017/2/20
Y1 - 2017/2/20
N2 - Elevated blood pressure is the leading heritable risk factor for cardiovascular disease worldwide. We report genetic association of blood pressure (systolic, diastolic, pulse pressure) among UK Biobank participants of European ancestry with independent replication in other cohorts, and robust validation of 107 independent loci. We also identify new independent variants at 11 previously reported blood pressure loci. In combination with results from a range of in silico functional analyses and wet bench experiments, our findings highlight new biological pathways for blood pressure regulation enriched for genes expressed in vascular tissues and identify potential therapeutic targets for hypertension. Results from genetic risk score models raise the possibility of a precision medicine approach through early lifestyle intervention to offset the impact of blood pressure-raising genetic variants on future cardiovascular disease risk.
AB - Elevated blood pressure is the leading heritable risk factor for cardiovascular disease worldwide. We report genetic association of blood pressure (systolic, diastolic, pulse pressure) among UK Biobank participants of European ancestry with independent replication in other cohorts, and robust validation of 107 independent loci. We also identify new independent variants at 11 previously reported blood pressure loci. In combination with results from a range of in silico functional analyses and wet bench experiments, our findings highlight new biological pathways for blood pressure regulation enriched for genes expressed in vascular tissues and identify potential therapeutic targets for hypertension. Results from genetic risk score models raise the possibility of a precision medicine approach through early lifestyle intervention to offset the impact of blood pressure-raising genetic variants on future cardiovascular disease risk.
U2 - 10.1038/ng.3768
DO - 10.1038/ng.3768
M3 - Journal article
C2 - 28135244
VL - 49
SP - 403
EP - 415
JO - Nature Genetics
JF - Nature Genetics
SN - 1061-4036
ER -