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International Consortium for Blood Pressure Genome-Wide Association Studies; Ehret, GB; Munroe, PB; Rice, KM; Bochud, M; Johnson, AD; Chasman, DI; Smith, AV; Tobin, MD; Verwoert, GC; Hwang, SJ; Pihur, V; Vollenweider, P; O'Reilly, PF; Amin, N; Bragg-Gresham, JL; Teumer, A; Glazer, NL; Launer, L; Zhao, JH; Aulchenko, Y; Heath, S; Sõber, S; Parsa, A; Luan, J; Arora, P; Dehghan, A; Zhang, F; Lucas, G; Hicks, AA; Jackson, AU; Peden, JF; Tanaka, T; Wild, SH; Rudan, I; Igl, W; Milaneschi, Y; Parker, AN; Fava, C; Chambers, JC; Fox, ER; Kumari, M; Go, MJ; van der Harst, P; Kao, WH; Sjögren, M; Vinay, DG; Alexander, M; Tabara, Y; Shaw-Hawkins, S; Whincup, PH; Liu, Y; Shi, G; Kuusisto, J; Tayo, B; Seielstad, M; Sim, X; Nguyen, KD; Lehtimäki, T; Matullo, G; Wu, Y; Gaunt, TR; Onland-Moret, NC; Cooper, MN; Platou, CG; Org, E; Hardy, R; Dahgam, S; Palmen, J; Vitart, V; Braund, PS; Kuznetsova, T; Uiterwaal, CS; Adeyemo, A; Palmas, W; Campbell, H; Ludwig, B; Tomaszewski, M; Tzoulaki, I; Palmer, ND; CARDIoGRAM consortium; CKDGen Consortium; KidneyGen Consortium; EchoGen consortium; CHARGE-HF consortium; Aspelund, T; Garcia, M; Chang, YP; O'Connell, JR; Steinle, NI; Grobbee, DE; Arking, DE; Kardia, SL; Morrison, AC; Hernandez, D; Najjar, S; McArdle, WL; Hadley, D; Brown, MJ; Connell, JM; Hingorani, AD; Day, IN; Lawlor, DA; Beilby, JP; Lawrence, RW; Clarke, R; Hopewell, JC; Ongen, H; Dreisbach, AW; Li, Y; Young, JH; Bis, JC; Kähönen, M; Viikari, J; Adair, LS; Lee, NR; Chen, MH; Olden, M; Pattaro, C; Bolton, JA; Köttgen, A; Bergmann, S; Mooser, V; Chaturvedi, N; Frayling, TM; Islam, M; Jafar, TH; Erdmann, J; Kulkarni, SR; Bornstein, SR; Grässler, J; Groop, L; Voight, BF; Kettunen, J; Howard, P; Taylor, A; Guarrera, S; Ricceri, F; Emilsson, V; Plump, A; Barroso, I; Khaw, KT; Weder, AB; Hunt, SC; Sun, YV; Bergman, RN; Collins, FS; Bonnycastle, LL; Scott, LJ; Stringham, HM; Peltonen, L; Perola, M; Vartiainen, E; Brand, SM; Staessen, JA; Wang, TJ; Burton, PR; Soler Artigas, M; Dong, Y; Snieder, H; Wang, X; Zhu, H; Lohman, KK; Rudock, ME; Heckbert, SR; Smith, NL; Wiggins, KL; Doumatey, A; Shriner, D; Veldre, G; Viigimaa, M; Kinra, S; Prabhakaran, D; Tripathy, V; Langefeld, CD; Rosengren, A; Thelle, DS; Corsi, AM; Singleton, A; Forrester, T; Hilton, G; McKenzie, CA; Salako, T; Iwai, N; Kita, Y; Ogihara, T; Ohkubo, T; Okamura, T; Ueshima, H; Umemura, S; Eyheramendy, S; Meitinger, T; Wichmann, HE; Cho, YS; Kim, HL; Lee, JY; Scott, J; Sehmi, JS; Zhang, W; Hedblad, B; Nilsson, P; Smith, GD; Wong, A; Narisu, N; Stančáková, A; Raffel, LJ; Yao, J; Kathiresan, S; O'Donnell, CJ; Schwartz, SM; Ikram, MA; Longstreth, WT; Mosley, TH; Seshadri, S; Shrine, NR; Wain, LV; Morken, MA; Swift, AJ; Laitinen, J; Prokopenko, I; Zitting, P; Cooper, JA; Humphries, SE; Danesh, J; Rasheed, A; Goel, A; Hamsten, A; Watkins, H; Bakker, SJ; van Gilst, WH; Janipalli, CS; Mani, KR; Yajnik, CS; Hofman, A; Mattace-Raso, FU; Oostra, BA; Demirkan, A; Isaacs, A; Rivadeneira, F; Lakatta, EG; Orru, M; Scuteri, A; Ala-Korpela, M; Kangas, AJ; Lyytikäinen, LP; Soininen, P; Tukiainen, T; Würtz, P; Ong, RT; Dörr, M; Kroemer, HK; Völker, U; Völzke, H; Galan, P; Hercberg, S; Lathrop, M; Zelenika, D; Deloukas, P; Mangino, M; Spector, TD; Zhai, G; Meschia, JF; Nalls, MA; Sharma, P; Terzic, J; Kumar, MV; Denniff, M; Zukowska-Szczechowska, E; Wagenknecht, LE; Fowkes, FG; Charchar, FJ; Schwarz, PE; Hayward, C; Guo, X; Rotimi, C; Bots, ML; Brand, E; Samani, NJ; Polasek, O; Talmud, PJ; Nyberg, F; Kuh, D; Laan, M; ....
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature. 2011; 478(7367):103-109 Doi: 10.1038/nature10405 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Study Group Mitglieder der Med Uni Graz:
Cavalieri Margherita
Dobnig Harald
März Winfried
Meinitzer Andreas
Pilz Stefan
Renner Wilfried
Scharnagl Hubert
Schmidt Helena
Schmidt Reinhold
Stojakovic Tatjana
Tomaschitz Andreas
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Abstract:
Blood pressure is a heritable trait influenced by several biological pathways and responsive to environmental stimuli. Over one billion people worldwide have hypertension (≥140 mm Hg systolic blood pressure or  ≥90 mm Hg diastolic blood pressure). Even small increments in blood pressure are associated with an increased risk of cardiovascular events. This genome-wide association study of systolic and diastolic blood pressure, which used a multi-stage design in 200,000 individuals of European descent, identified sixteen novel loci: six of these loci contain genes previously known or suspected to regulate blood pressure (GUCY1A3-GUCY1B3, NPR3-C5orf23, ADM, FURIN-FES, GOSR2, GNAS-EDN3); the other ten provide new clues to blood pressure physiology. A genetic risk score based on 29 genome-wide significant variants was associated with hypertension, left ventricular wall thickness, stroke and coronary artery disease, but not kidney disease or kidney function. We also observed associations with blood pressure in East Asian, South Asian and African ancestry individuals. Our findings provide new insights into the genetics and biology of blood pressure, and suggest potential novel therapeutic pathways for cardiovascular disease prevention.
Find related publications in this database (using NLM MeSH Indexing)
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Blood Pressure - genetics
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Genetic Predisposition to Disease - genetics
Genome-Wide Association Study -
Humans -
Hypertension - genetics
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