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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Helen R. Warren, Εvangelos Εvangelou, Claudia P. Cabrera, He Gao, Meixia Ren, Borbála Mifsud, Ioanna Ntalla, Praveen Surendran, Chunyu Liu, James P. Cook, Aldi T. Kraja, Fotios Drenos, Marie Chiew Shia Loh, Niek Verweij, Jonathan Marten, İbrahim Karaman, Marcelo P. Segura-Lepe, Paul F. O’Reilly, Jo Knight, Harold Snieder, Norihiro Kato, Jiang He, E Shyong Tai, M. Abdullah Said, David John Porteous, Maris Alver, Neil R Poulter, Martin Farrall, Ron T. Gansevoort, Sandosh Padmanabhan

📄 Abstract

Mark Caulfield, Paul Elliott and colleagues use data from the UK Biobank to perform genome-wide association analysis for blood pressure traits. They identify and validate 107 novel loci and highlight new biological pathways for potential therapeutic intervention for hypertension. 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.

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