Literature DB >> 22042884

Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.

Nora Franceschini1, Cara Carty, Petra Bůzková, Alex P Reiner, Tiana Garrett, Yi Lin, Jens-S Vöckler, Lucia A Hindorff, Shelley A Cole, Eric Boerwinkle, Dan-Yu Lin, Ebony Bookman, Lyle G Best, Jonathan N Bella, Charles Eaton, Philip Greenland, Nancy Jenny, Kari E North, Darin Taverna, Alicia M Young, Ewa Deelman, Charles Kooperberg, Bruce Psaty, Gerardo Heiss.   

Abstract

BACKGROUND: Genome-wide association studies identified several single nucleotide polymorphisms (SNP) associated with prevalent coronary heart disease (CHD), but less is known of associations with incident CHD. The association of 13 published CHD SNPs was examined in 5 ancestry groups of 4 large US prospective cohorts. METHODS AND
RESULTS: The analyses included incident coronary events over an average 9.1 to 15.7 follow-up person-years in up to 26 617 white individuals (6626 events), 8018 black individuals (914 events), 1903 Hispanic individuals (113 events), 3669 American Indian individuals (595 events), and 885 Asian/Pacific Islander individuals (66 events). We used Cox proportional hazards models (with additive mode of inheritance) adjusted for age, sex, and ancestry (as needed). Nine loci were statistically associated with incident CHD events in white participants: 9p21 (rs10757278; P=4.7 × 10(-41)), 16q23.1 (rs2549513; P=0.0004), 6p24.1 (rs499818; P=0.0002), 2q36.3 (rs2943634; P=6.7 × 10(-6)), MTHFD1L (rs6922269, P=5.1 × 10(-10)), APOE (rs429358; P=2.7×10(-18)), ZNF627 (rs4804611; P=5.0 × 10(-8)), CXCL12 (rs501120; P=1.4 × 10(-6)) and LPL (rs268; P=2.7 × 10(-17)). The 9p21 region showed significant between-study heterogeneity, with larger effects in individuals age 55 years or younger and in women. Inclusion of coronary revascularization procedures among the incident CHD events introduced heterogeneity. The SNPs were not associated with CHD in black participants, and associations varied in other US minorities.
CONCLUSIONS: Prospective analyses of white participants replicated several reported cross-sectional CHD-SNP associations.

Entities:  

Mesh:

Year:  2011        PMID: 22042884      PMCID: PMC3293207          DOI: 10.1161/CIRCGENETICS.111.960096

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN: 1942-3268


  43 in total

1.  Polymorphisms associated with cholesterol and risk of cardiovascular events.

Authors:  Sekar Kathiresan; Olle Melander; Dragi Anevski; Candace Guiducci; Noël P Burtt; Charlotta Roos; Joel N Hirschhorn; Göran Berglund; Bo Hedblad; Leif Groop; David M Altshuler; Christopher Newton-Cheh; Marju Orho-Melander
Journal:  N Engl J Med       Date:  2008-03-20       Impact factor: 91.245

2.  A common variant on chromosome 9p21 affects the risk of myocardial infarction.

Authors:  Anna Helgadottir; Gudmar Thorleifsson; Andrei Manolescu; Solveig Gretarsdottir; Thorarinn Blondal; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Asgeir Sigurdsson; Adam Baker; Arnar Palsson; Gisli Masson; Daniel F Gudbjartsson; Kristinn P Magnusson; Karl Andersen; Allan I Levey; Valgerdur M Backman; Sigurborg Matthiasdottir; Thorbjorg Jonsdottir; Stefan Palsson; Helga Einarsdottir; Steinunn Gunnarsdottir; Arnaldur Gylfason; Viola Vaccarino; W Craig Hooper; Muredach P Reilly; Christopher B Granger; Harland Austin; Daniel J Rader; Svati H Shah; Arshed A Quyyumi; Jeffrey R Gulcher; Gudmundur Thorgeirsson; Unnur Thorsteinsdottir; Augustine Kong; Kari Stefansson
Journal:  Science       Date:  2007-05-03       Impact factor: 47.728

3.  The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.

Authors:  Anna Helgadottir; Gudmar Thorleifsson; Kristinn P Magnusson; Solveig Grétarsdottir; Valgerdur Steinthorsdottir; Andrei Manolescu; Gregory T Jones; Gabriel J E Rinkel; Jan D Blankensteijn; Antti Ronkainen; Juha E Jääskeläinen; Yoshiki Kyo; Guy M Lenk; Natzi Sakalihasan; Konstantinos Kostulas; Anders Gottsäter; Andrea Flex; Hreinn Stefansson; Torben Hansen; Gitte Andersen; Shantel Weinsheimer; Knut Borch-Johnsen; Torben Jorgensen; Svati H Shah; Arshed A Quyyumi; Christopher B Granger; Muredach P Reilly; Harland Austin; Allan I Levey; Viola Vaccarino; Ebba Palsdottir; G Bragi Walters; Thorbjorg Jonsdottir; Steinunn Snorradottir; Dana Magnusdottir; Gudmundur Gudmundsson; Robert E Ferrell; Sigurlaug Sveinbjornsdottir; Juha Hernesniemi; Mika Niemelä; Raymond Limet; Karl Andersen; Gunnar Sigurdsson; Rafn Benediktsson; Eric L G Verhoeven; Joep A W Teijink; Diederick E Grobbee; Daniel J Rader; David A Collier; Oluf Pedersen; Roberto Pola; Jan Hillert; Bengt Lindblad; Einar M Valdimarsson; Hulda B Magnadottir; Cisca Wijmenga; Gerard Tromp; Annette F Baas; Ynte M Ruigrok; Andre M van Rij; Helena Kuivaniemi; Janet T Powell; Stefan E Matthiasson; Jeffrey R Gulcher; Gudmundur Thorgeirsson; Augustine Kong; Unnur Thorsteinsdottir; Kari Stefansson
Journal:  Nat Genet       Date:  2008-01-06       Impact factor: 38.330

4.  A common allele on chromosome 9 associated with coronary heart disease.

Authors:  Ruth McPherson; Alexander Pertsemlidis; Nihan Kavaslar; Alexandre Stewart; Robert Roberts; David R Cox; David A Hinds; Len A Pennacchio; Anne Tybjaerg-Hansen; Aaron R Folsom; Eric Boerwinkle; Helen H Hobbs; Jonathan C Cohen
Journal:  Science       Date:  2007-05-03       Impact factor: 47.728

5.  Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations.

Authors:  Kunihiko Hinohara; Toshiaki Nakajima; Megumi Takahashi; Shigeru Hohda; Taishi Sasaoka; Ken-Ichi Nakahara; Kouji Chida; Motoji Sawabe; Takuro Arimura; Akinori Sato; Bok-Soo Lee; Ji-Min Ban; Michio Yasunami; Jeong-Euy Park; Toru Izumi; Akinori Kimura
Journal:  J Hum Genet       Date:  2008-02-09       Impact factor: 3.172

6.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Authors: 
Journal:  Nature       Date:  2007-06-07       Impact factor: 49.962

7.  Genomewide association analysis of coronary artery disease.

Authors:  Nilesh J Samani; Jeanette Erdmann; Alistair S Hall; Christian Hengstenberg; Massimo Mangino; Bjoern Mayer; Richard J Dixon; Thomas Meitinger; Peter Braund; H-Erich Wichmann; Jennifer H Barrett; Inke R König; Suzanne E Stevens; Silke Szymczak; David-Alexandre Tregouet; Mark M Iles; Friedrich Pahlke; Helen Pollard; Wolfgang Lieb; Francois Cambien; Marcus Fischer; Willem Ouwehand; Stefan Blankenberg; Anthony J Balmforth; Andrea Baessler; Stephen G Ball; Tim M Strom; Ingrid Braenne; Christian Gieger; Panos Deloukas; Martin D Tobin; Andreas Ziegler; John R Thompson; Heribert Schunkert
Journal:  N Engl J Med       Date:  2007-07-18       Impact factor: 91.245

8.  Newly identified loci that influence lipid concentrations and risk of coronary artery disease.

Authors:  Cristen J Willer; Serena Sanna; Anne U Jackson; Angelo Scuteri; Lori L Bonnycastle; Robert Clarke; Simon C Heath; Nicholas J Timpson; Samer S Najjar; Heather M Stringham; James Strait; William L Duren; Andrea Maschio; Fabio Busonero; Antonella Mulas; Giuseppe Albai; Amy J Swift; Mario A Morken; Narisu Narisu; Derrick Bennett; Sarah Parish; Haiqing Shen; Pilar Galan; Pierre Meneton; Serge Hercberg; Diana Zelenika; Wei-Min Chen; Yun Li; Laura J Scott; Paul A Scheet; Jouko Sundvall; Richard M Watanabe; Ramaiah Nagaraja; Shah Ebrahim; Debbie A Lawlor; Yoav Ben-Shlomo; George Davey-Smith; Alan R Shuldiner; Rory Collins; Richard N Bergman; Manuela Uda; Jaakko Tuomilehto; Antonio Cao; Francis S Collins; Edward Lakatta; G Mark Lathrop; Michael Boehnke; David Schlessinger; Karen L Mohlke; Gonçalo R Abecasis
Journal:  Nat Genet       Date:  2008-01-13       Impact factor: 38.330

9.  Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.

Authors:  Martin G Larson; Larry D Atwood; Emelia J Benjamin; L Adrienne Cupples; Ralph B D'Agostino; Caroline S Fox; Diddahally R Govindaraju; Chao-Yu Guo; Nancy L Heard-Costa; Shih-Jen Hwang; Joanne M Murabito; Christopher Newton-Cheh; Christopher J O'Donnell; Sudha Seshadri; Ramachandran S Vasan; Thomas J Wang; Philip A Wolf; Daniel Levy
Journal:  BMC Med Genet       Date:  2007-09-19       Impact factor: 2.103

10.  Heterogeneity in meta-analyses of genome-wide association investigations.

Authors:  John P A Ioannidis; Nikolaos A Patsopoulos; Evangelos Evangelou
Journal:  PLoS One       Date:  2007-09-05       Impact factor: 3.240

View more
  32 in total

Review 1.  Genome-Wide Association Studies of Coronary Artery Disease: Recent Progress and Challenges Ahead.

Authors:  Shoa L Clarke; Themistocles L Assimes
Journal:  Curr Atheroscler Rep       Date:  2018-07-18       Impact factor: 5.113

2.  Prospective association of a genetic risk score and lifestyle intervention with cardiovascular morbidity and mortality among individuals with type 2 diabetes: the Look AHEAD randomised controlled trial.

Authors: 
Journal:  Diabetologia       Date:  2015-05-14       Impact factor: 10.122

3.  Genetic Epidemiologic Analysis of Hypertensive Retinopathy in an Underrepresented and Rare Federally Recognized Native American Population of the Intermountain West.

Authors:  Patrice M Hicks; Samuel A Collazo Melendez; Albert Vitale; William Self; Mary Elizabeth Hartnett; Paul Bernstein; Denise J Morgan; Michael Feehan; Akbar Shakoor; Ivana Kim; Leah A Owen; Margaret M DeAngelis
Journal:  J Community Med Public Health       Date:  2019-06-10

4.  Clinical application of chromosome 9p21.3 genotyping in patients with coronary artery disease.

Authors:  Svetlana Nikulina; Ivan Artyukhov; Pavel Shesternya; Oksana Gavrilyuk; Vladimir Maksimov; Mikhail Voyevoda; Denis Brusentsov
Journal:  Exp Ther Med       Date:  2019-08-13       Impact factor: 2.447

Review 5.  Genetics of coronary artery disease.

Authors:  Wolfgang Lieb; Ramachandran S Vasan
Journal:  Circulation       Date:  2013-09-03       Impact factor: 29.690

Review 6.  How Genomics Is Personalizing the Management of Dyslipidemia and Cardiovascular Disease Prevention.

Authors:  Lane B Benes; Daniel J Brandt; Eric J Brandt; Michael H Davidson
Journal:  Curr Cardiol Rep       Date:  2018-10-17       Impact factor: 2.931

7.  Rs6922269 marker at the MTHFD1L gene predict cardiovascular mortality in males after acute coronary syndrome.

Authors:  J A Hubacek; V Staněk; M Gebauerová; R Poledne; M Aschermann; H Skalická; J Matoušková; A Kruger; M Pěnička; H Hrabáková; J Veselka; P Hájek; V Lánská; V Adámková; J Pitˇha
Journal:  Mol Biol Rep       Date:  2015-03-26       Impact factor: 2.316

8.  Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study.

Authors:  Lili Zhang; Petra Buzkova; Christina L Wassel; Mary J Roman; Kari E North; Dana C Crawford; Jonathan Boston; Kristin D Brown-Gentry; Shelley A Cole; Ewa Deelman; Robert Goodloe; Sarah Wilson; Gerardo Heiss; Nancy S Jenny; Neal W Jorgensen; Tara C Matise; Bob E McClellan; Alejandro Q Nato; Marylyn D Ritchie; Nora Franceschini; W H Linda Kao
Journal:  Atherosclerosis       Date:  2013-03-13       Impact factor: 5.162

9.  The association between the DNAH11 rs10248618 SNP and serum lipid traits, the risk of coronary artery disease, and ischemic stroke.

Authors:  Yong-Gang Zhou; Rui-Xing Yin; Jie Wu; Qing-Hui Zhang; Wu-Xian Chen; Xiao-Li Cao
Journal:  Int J Clin Exp Pathol       Date:  2018-09-01

10.  The SNP rs4804611 in ZNF627 gene and the risk of myocardial infarction: a meta-analysis.

Authors:  Nan Wu; Xiaowen Zhang; Pengyu Jia; Dalin Jia
Journal:  Int J Clin Exp Med       Date:  2015-04-15
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.