Abstract
BACKGROUND: The presence of an early repolarization pattern (ERP) on the surface ECG is associated with risk of ventricular fibrillation and sudden cardiac death. Family studies have shown that ERP is a highly heritable trait, but molecular genetic determinants are unknown. METHODS: To identify genetic susceptibility loci for ERP, we performed a GWAS and meta-analysis in 2,181 cases and 23,641 controls of European ancestry. RESULTS. We identified a genome-wide significant (P < 5 × 10 -8) locus in the potassium voltage-gated channel subfamily D member 3 (KCND3) gene that was successfully replicated in additional 1,124 cases and 12,510 controls. A subsequent joint meta-analysis of the discovery and replication cohorts identified rs1545300 as the lead SNP at the KCND3 locus (OR 0.82 per minor T allele, P = 7.7 × 10-12) but did not reveal additional loci. Colocalization analyses indicate causal effects of KCND3 gene expression levels on ERP in both cardiac left ventricle and tibial artery. CONCLUSIONS: In this study, we identified for the first time to our knowledge a genome-wide significant association of a genetic variant with ERP. Our findings of a locus in the KCND3 gene provide insights not only into the genetic determinants but also into the pathophysiological mechanism of ERP, discovering a promising candidate for functional studies.
| Original language | English |
|---|---|
| Article number | e131156 |
| Journal | JCI Insight |
| Volume | 4 |
| Issue number | 23 |
| DOIs | |
| Publication status | Published - 5 Dec 2019 |
Keywords
- Alleles
- Death, Sudden, Cardiac
- Electrocardiography/methods
- Female
- Genetic Loci
- Genetic Predisposition to Disease/genetics
- Genome-Wide Association Study/methods
- Genotype
- Heart Ventricles
- Humans
- Male
- Polymorphism, Single Nucleotide
- Shal Potassium Channels/genetics
- Transcriptome
- Ventricular Fibrillation/genetics
- Whites/genetics