Recent genome-wide association studies (GWAS) have identified novel loci associated with sudden cardiac death (SCD). Despite this progress, identified DNA variants account for a relatively small portion of overall SCD risk, suggesting that additional loci contributing to SCD susceptibility await discovery. The objective of this study was to identify novel DNA variation associated with SCD in the context of coronary artery disease (CAD).Using the MetaboChip custom array we conducted a case-control association analysis of 119,117 SNPs in 948 SCD cases (with underlying CAD) from the Oregon Sudden Unexpected Death Study (Oregon-SUDS) and 3,050 controls with CAD from the Wellcome Trust Case-Control Consortium (WTCCC). Two newly identified loci were significantly associated with increased risk of SCD after correction for multiple comparisons at: rs6730157 in the RAB3GAP1 gene on chromosome 2 (P = 4.93×10(-12), OR = 1.60) and rs2077316 in the ZNF365 gene on chromosome 10 (P = 3.64×10(-8), OR = 2.41).Our findings suggest that RAB3GAP1 and ZNF365 are relevant candidate genes for SCD and will contribute to the mechanistic understanding of SCD susceptibility.

Original publication

DOI

10.1371/journal.pone.0059905

Type

Journal article

Journal

PloS one

Publication Date

01/2013

Volume

8

Addresses

The Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.

Keywords

WTCCC+, Humans, Death, Sudden, Cardiac, Genetic Predisposition to Disease, rab3 GTP-Binding Proteins, DNA-Binding Proteins, Transcription Factors, Risk, Case-Control Studies, Polymorphism, Single Nucleotide, Introns, Adult, Aged, Middle Aged, Female, Male, Coronary Artery Disease, Genetic Loci