Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis

Pradeep Natarajan, Joshua C. Bis, Lawrence F. Bielak, Amanda J. Cox, Marcus Dörr, Mary F. Feitosa, Nora Franceschini, Xiuqing Guo, Shih Jen Hwang, Aaron Isaacs, Min A. Jhun, Maryam Kavousi, Ruifang Li-Gao, Leo Pekka Lyytikäinen, Riccardo E. Marioni, Ulf Schminke, Nathan O. Stitziel, Hayato Tada, Jessica Van Setten, Albert V. SmithDina Vojinovic, Lisa R. Yanek, Jie Yao, Laura M. Yerges-Armstrong, Najaf Amin, Usman Baber, Ingrid B. Borecki, J. Jeffrey Carr, Yii Der Ida Chen, L. Adrienne Cupples, Pim A. De Jong, Harry De Koning, Bob D. De Vos, Ayse Demirkan, Valentin Fuster, Oscar H. Franco, Mark O. Goodarzi, Tamara B. Harris, Susan R. Heckbert, Gerardo Heiss, Udo Hoffmann, Albert Hofman, Ivana Išgum, J. Wouter Jukema, Mika Kähönen, Sharon L R Kardia, Brian G. Kral, Lenore J. Launer, Joe Massaro, Roxana Mehran, Braxton D. Mitchell, Thomas H. Mosley, Renée De Mutsert, Anne B. Newman, Khanh Dung Nguyen, Kari E. North, Jeffrey R. O'Connell, Matthijs Oudkerk, James S. Pankow, Gina M. Peloso, Wendy Post, Michael A. Province, Laura M. Raffield, Olli T. Raitakari, Dermot F. Reilly, Fernando Rivadeneira, Frits Rosendaal, Samantha Sartori, Kent D. Taylor, Alexander Teumer, Stella Trompet, Stephen T. Turner, Andre G. Uitterlinden, Dhananjay Vaidya, Aad Van Der Lugt, Uwe Völker, Joanna M. Wardlaw, Christina L. Wassel, Stefan Weiss, Mary K. Wojczynski, Diane M. Becker, Lewis C. Becker, Eric Boerwinkle, Donald W. Bowden, Ian J. Deary, Abbas Dehghan, Stephan B. Felix, Vilmundur Gudnason, Terho Lehtimäki, Rasika Mathias, Dennis O. Mook-Kanamori, Bruce M. Psaty, Daniel J. Rader, Jerome I. Rotter, James G. Wilson, Cornelia M. Van Duijn, Henry Völzke, Sekar Kathiresan, Patricia A. Peyser, Christopher J. O'Donnell

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Background-The burden of subclinical atherosclerosis in asymptomatic individuals is heritable and associated with elevated risk of developing clinical coronary heart disease. We sought to identify genetic variants in protein-coding regions associated with subclinical atherosclerosis and the risk of subsequent coronary heart disease. Methods and Results-We studied a total of 25 109 European ancestry and African ancestry participants with coronary artery calcification (CAC) measured by cardiac computed tomography and 52 869 participants with common carotid intima-media thickness measured by ultrasonography within the CHARGE Consortium (Cohorts for Heart and Aging Research in Genomic Epidemiology). Participants were genotyped for 247 870 DNA sequence variants (231 539 in exons) across the genome. A meta-analysis of exome-wide association studies was performed across cohorts for CAC and carotid intima-media thickness. APOB p.Arg3527Gln was associated with 4-fold excess CAC (P=3×10-10). The APOE ϵ2 allele (p.Arg176Cys) was associated with both 22.3% reduced CAC (P=1×10-12) and 1.4% reduced carotid intima-media thickness (P=4×10-14) in carriers compared with noncarriers. In secondary analyses conditioning on low-density lipoprotein cholesterol concentration, the ϵ2 protective association with CAC, although attenuated, remained strongly significant. Additionally, the presence of ϵ2 was associated with reduced risk for coronary heart disease (odds ratio 0.77; P=1×10-11). Conclusions-Exome-wide association meta-analysis demonstrates that protein-coding variants in APOB and APOE associate with subclinical atherosclerosis. APOE ϵ2 represents the first significant association for multiple subclinical atherosclerosis traits across multiple ethnicities, as well as clinical coronary heart disease.

Original languageEnglish (US)
Pages (from-to)511-520
Number of pages10
JournalCirculation: Cardiovascular Genetics
Volume9
Issue number6
DOIs
StatePublished - Dec 1 2016

Keywords

  • carotid intima-media thickness
  • coronary artery calcification
  • exome
  • genome-wide association study
  • genomics

Fingerprint Dive into the research topics of 'Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis'. Together they form a unique fingerprint.

Cite this