Research
Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital
Published

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kato, N, Loh, M, Takeuchi, F, Verweij, N, Wang, X, Zhang, W, Kelly, TN, Saleheen, D, Lehne, B, Mateo Leach, I, Drong, AW, Abbott, J, Wahl, S, Tan, S-T, Scott, WR, Campanella, G, Chadeau-Hyam, M, Afzal, U, Ahluwalia, TS, Bonder, MJ, Chen, P, Dehghan, A, Edwards, TL, Esko, T, Go, MJ, Harris, SE, Hartiala, J, Kasela, S, Kasturiratne, A, Khor, C-C, Kleber, ME, Li, H, Mok, ZY, Nakatochi, M, Sapari, NS, Saxena, R, Stewart, AFR, Stolk, L, Tabara, Y, Teh, AL, Wu, Y, Wu, J-Y, Zhang, Y, Aits, I, Husemoen, LLN, Sparsø, T, Hansen, T, Jørgensen, T, Linneberg, A, Sørensen, TIA & BIOS-consortium 2015, 'Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation' Nature Genetics, vol. 47, no. 11, pp. 1282-93. https://doi.org/10.1038/ng.3405

APA

CBE

Kato N, Loh M, Takeuchi F, Verweij N, Wang X, Zhang W, Kelly TN, Saleheen D, Lehne B, Mateo Leach I, Drong AW, Abbott J, Wahl S, Tan S-T, Scott WR, Campanella G, Chadeau-Hyam M, Afzal U, Ahluwalia TS, Bonder MJ, Chen P, Dehghan A, Edwards TL, Esko T, Go MJ, Harris SE, Hartiala J, Kasela S, Kasturiratne A, Khor C-C, Kleber ME, Li H, Mok ZY, Nakatochi M, Sapari NS, Saxena R, Stewart AFR, Stolk L, Tabara Y, Teh AL, Wu Y, Wu J-Y, Zhang Y, Aits I, Husemoen LLN, Sparsø T, Hansen T, Jørgensen T, Linneberg A, Sørensen TIA, BIOS-consortium. 2015. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nature Genetics. 47(11):1282-93. https://doi.org/10.1038/ng.3405

MLA

Vancouver

Author

Kato, Norihiro ; Loh, Marie ; Takeuchi, Fumihiko ; Verweij, Niek ; Wang, Xu ; Zhang, Weihua ; Kelly, Tanika N ; Saleheen, Danish ; Lehne, Benjamin ; Mateo Leach, Irene ; Drong, Alexander W ; Abbott, James ; Wahl, Simone ; Tan, Sian-Tsung ; Scott, William R ; Campanella, Gianluca ; Chadeau-Hyam, Marc ; Afzal, Uzma ; Ahluwalia, Tarunveer S ; Bonder, Marc Jan ; Chen, Peng ; Dehghan, Abbas ; Edwards, Todd L ; Esko, Tõnu ; Go, Min Jin ; Harris, Sarah E ; Hartiala, Jaana ; Kasela, Silva ; Kasturiratne, Anuradhani ; Khor, Chiea-Chuen ; Kleber, Marcus E ; Li, Huaixing ; Mok, Zuan Yu ; Nakatochi, Masahiro ; Sapari, Nur Sabrina ; Saxena, Richa ; Stewart, Alexandre F R ; Stolk, Lisette ; Tabara, Yasuharu ; Teh, Ai Ling ; Wu, Ying ; Wu, Jer-Yuarn ; Zhang, Yi ; Aits, Imke ; Husemoen, Lise L N ; Sparsø, Thomas ; Hansen, Torben ; Jørgensen, Torben ; Linneberg, Allan ; Sørensen, Thorkild I A ; BIOS-consortium. / Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. In: Nature Genetics. 2015 ; Vol. 47, No. 11. pp. 1282-93.

Bibtex

@article{48b4fd4005324aceaa5759cabb34f32f,
title = "Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation",
abstract = "We carried out a trans-ancestry genome-wide association and replication study of blood pressure phenotypes among up to 320,251 individuals of East Asian, European and South Asian ancestry. We find genetic variants at 12 new loci to be associated with blood pressure (P = 3.9 × 10(-11) to 5.0 × 10(-21)). The sentinel blood pressure SNPs are enriched for association with DNA methylation at multiple nearby CpG sites, suggesting that, at some of the loci identified, DNA methylation may lie on the regulatory pathway linking sequence variation to blood pressure. The sentinel SNPs at the 12 new loci point to genes involved in vascular smooth muscle (IGFBP3, KCNK3, PDE3A and PRDM6) and renal (ARHGAP24, OSR1, SLC22A7 and TBX2) function. The new and known genetic variants predict increased left ventricular mass, circulating levels of NT-proBNP, and cardiovascular and all-cause mortality (P = 0.04 to 8.6 × 10(-6)). Our results provide new evidence for the role of DNA methylation in blood pressure regulation.",
author = "Norihiro Kato and Marie Loh and Fumihiko Takeuchi and Niek Verweij and Xu Wang and Weihua Zhang and Kelly, {Tanika N} and Danish Saleheen and Benjamin Lehne and {Mateo Leach}, Irene and Drong, {Alexander W} and James Abbott and Simone Wahl and Sian-Tsung Tan and Scott, {William R} and Gianluca Campanella and Marc Chadeau-Hyam and Uzma Afzal and Ahluwalia, {Tarunveer S} and Bonder, {Marc Jan} and Peng Chen and Abbas Dehghan and Edwards, {Todd L} and T{\~o}nu Esko and Go, {Min Jin} and Harris, {Sarah E} and Jaana Hartiala and Silva Kasela and Anuradhani Kasturiratne and Chiea-Chuen Khor and Kleber, {Marcus E} and Huaixing Li and Mok, {Zuan Yu} and Masahiro Nakatochi and Sapari, {Nur Sabrina} and Richa Saxena and Stewart, {Alexandre F R} and Lisette Stolk and Yasuharu Tabara and Teh, {Ai Ling} and Ying Wu and Jer-Yuarn Wu and Yi Zhang and Imke Aits and Husemoen, {Lise L N} and Thomas Spars{\o} and Torben Hansen and Torben J{\o}rgensen and Allan Linneberg and S{\o}rensen, {Thorkild I A} and BIOS-consortium",
year = "2015",
month = "11",
doi = "10.1038/ng.3405",
language = "English",
volume = "47",
pages = "1282--93",
journal = "Nature Genetics",
issn = "1061-4036",
publisher = "Nature Publishing Group",
number = "11",

}

RIS

TY - JOUR

T1 - Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

AU - Kato, Norihiro

AU - Loh, Marie

AU - Takeuchi, Fumihiko

AU - Verweij, Niek

AU - Wang, Xu

AU - Zhang, Weihua

AU - Kelly, Tanika N

AU - Saleheen, Danish

AU - Lehne, Benjamin

AU - Mateo Leach, Irene

AU - Drong, Alexander W

AU - Abbott, James

AU - Wahl, Simone

AU - Tan, Sian-Tsung

AU - Scott, William R

AU - Campanella, Gianluca

AU - Chadeau-Hyam, Marc

AU - Afzal, Uzma

AU - Ahluwalia, Tarunveer S

AU - Bonder, Marc Jan

AU - Chen, Peng

AU - Dehghan, Abbas

AU - Edwards, Todd L

AU - Esko, Tõnu

AU - Go, Min Jin

AU - Harris, Sarah E

AU - Hartiala, Jaana

AU - Kasela, Silva

AU - Kasturiratne, Anuradhani

AU - Khor, Chiea-Chuen

AU - Kleber, Marcus E

AU - Li, Huaixing

AU - Mok, Zuan Yu

AU - Nakatochi, Masahiro

AU - Sapari, Nur Sabrina

AU - Saxena, Richa

AU - Stewart, Alexandre F R

AU - Stolk, Lisette

AU - Tabara, Yasuharu

AU - Teh, Ai Ling

AU - Wu, Ying

AU - Wu, Jer-Yuarn

AU - Zhang, Yi

AU - Aits, Imke

AU - Husemoen, Lise L N

AU - Sparsø, Thomas

AU - Hansen, Torben

AU - Jørgensen, Torben

AU - Linneberg, Allan

AU - Sørensen, Thorkild I A

AU - BIOS-consortium

PY - 2015/11

Y1 - 2015/11

N2 - We carried out a trans-ancestry genome-wide association and replication study of blood pressure phenotypes among up to 320,251 individuals of East Asian, European and South Asian ancestry. We find genetic variants at 12 new loci to be associated with blood pressure (P = 3.9 × 10(-11) to 5.0 × 10(-21)). The sentinel blood pressure SNPs are enriched for association with DNA methylation at multiple nearby CpG sites, suggesting that, at some of the loci identified, DNA methylation may lie on the regulatory pathway linking sequence variation to blood pressure. The sentinel SNPs at the 12 new loci point to genes involved in vascular smooth muscle (IGFBP3, KCNK3, PDE3A and PRDM6) and renal (ARHGAP24, OSR1, SLC22A7 and TBX2) function. The new and known genetic variants predict increased left ventricular mass, circulating levels of NT-proBNP, and cardiovascular and all-cause mortality (P = 0.04 to 8.6 × 10(-6)). Our results provide new evidence for the role of DNA methylation in blood pressure regulation.

AB - We carried out a trans-ancestry genome-wide association and replication study of blood pressure phenotypes among up to 320,251 individuals of East Asian, European and South Asian ancestry. We find genetic variants at 12 new loci to be associated with blood pressure (P = 3.9 × 10(-11) to 5.0 × 10(-21)). The sentinel blood pressure SNPs are enriched for association with DNA methylation at multiple nearby CpG sites, suggesting that, at some of the loci identified, DNA methylation may lie on the regulatory pathway linking sequence variation to blood pressure. The sentinel SNPs at the 12 new loci point to genes involved in vascular smooth muscle (IGFBP3, KCNK3, PDE3A and PRDM6) and renal (ARHGAP24, OSR1, SLC22A7 and TBX2) function. The new and known genetic variants predict increased left ventricular mass, circulating levels of NT-proBNP, and cardiovascular and all-cause mortality (P = 0.04 to 8.6 × 10(-6)). Our results provide new evidence for the role of DNA methylation in blood pressure regulation.

U2 - 10.1038/ng.3405

DO - 10.1038/ng.3405

M3 - Journal article

VL - 47

SP - 1282

EP - 1293

JO - Nature Genetics

JF - Nature Genetics

SN - 1061-4036

IS - 11

ER -

ID: 45752604