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Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium

Author

Listed:
  • Abbas Dehghan
  • Joshua C Bis
  • Charles C White
  • Albert Vernon Smith
  • Alanna C Morrison
  • L Adrienne Cupples
  • Stella Trompet
  • Daniel I Chasman
  • Thomas Lumley
  • Uwe Völker
  • Brendan M Buckley
  • Jingzhong Ding
  • Majken K Jensen
  • Aaron R Folsom
  • Stephen B Kritchevsky
  • Cynthia J Girman
  • Ian Ford
  • Marcus Dörr
  • Veikko Salomaa
  • André G Uitterlinden
  • Gudny Eiriksdottir
  • Ramachandran S Vasan
  • Nora Franceschini
  • Cara L Carty
  • Jarmo Virtamo
  • Serkalem Demissie
  • Philippe Amouyel
  • Dominique Arveiler
  • Susan R Heckbert
  • Jean Ferrières
  • Pierre Ducimetière
  • Nicholas L Smith
  • Ying A Wang
  • David S Siscovick
  • Kenneth M Rice
  • Per-Gunnar Wiklund
  • Kent D Taylor
  • Alun Evans
  • Frank Kee
  • Jerome I Rotter
  • Juha Karvanen
  • Kari Kuulasmaa
  • Gerardo Heiss
  • Peter Kraft
  • Lenore J Launer
  • Albert Hofman
  • Marcello R P Markus
  • Lynda M Rose
  • Kaisa Silander
  • Peter Wagner
  • Emelia J Benjamin
  • Kurt Lohman
  • David J Stott
  • Fernando Rivadeneira
  • Tamara B Harris
  • Daniel Levy
  • Yongmei Liu
  • Eric B Rimm
  • J Wouter Jukema
  • Henry Völzke
  • Paul M Ridker
  • Stefan Blankenberg
  • Oscar H Franco
  • Vilmundur Gudnason
  • Bruce M Psaty
  • Eric Boerwinkle
  • Christopher J O'Donnell

Abstract

Background: Data are limited on genome-wide association studies (GWAS) for incident coronary heart disease (CHD). Moreover, it is not known whether genetic variants identified to date also associate with risk of CHD in a prospective setting. Methods: We performed a two-stage GWAS analysis of incident myocardial infarction (MI) and CHD in a total of 64,297 individuals (including 3898 MI cases, 5465 CHD cases). SNPs that passed an arbitrary threshold of 5×10−6 in Stage I were taken to Stage II for further discovery. Furthermore, in an analysis of prognosis, we studied whether known SNPs from former GWAS were associated with total mortality in individuals who experienced MI during follow-up. Results: In Stage I 15 loci passed the threshold of 5×10−6; 8 loci for MI and 8 loci for CHD, for which one locus overlapped and none were reported in previous GWAS meta-analyses. We took 60 SNPs representing these 15 loci to Stage II of discovery. Four SNPs near QKI showed nominally significant association with MI (p-value

Suggested Citation

  • Abbas Dehghan & Joshua C Bis & Charles C White & Albert Vernon Smith & Alanna C Morrison & L Adrienne Cupples & Stella Trompet & Daniel I Chasman & Thomas Lumley & Uwe Völker & Brendan M Buckley & Jin, 2016. "Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium," PLOS ONE, Public Library of Science, vol. 11(3), pages 1-16, March.
  • Handle: RePEc:plo:pone00:0144997
    DOI: 10.1371/journal.pone.0144997
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    Cited by:

    1. Yi Sun & Shuna Huang & Qing Huang & Shaowei Lin & Siying Wu & Guiqing Wu & Qishuang Ruan & Tingxing Zhang & Huangyuan Li, 2018. "Microarray Analysis of Differentially Expressed LncRNAs with Associated Co-Expression and CeRNA Networks in Coronary Heart Disease," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 3(2), pages 3197-3207, March.

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