KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern

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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 languageEnglish
Article numbere131156
JournalJCI Insight
Volume4
Issue number23
DOIs
Publication statusPublished - 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

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