TY - JOUR
T1 - KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern
AU - Teumer, Alexander
AU - Trenkwalder, Teresa
AU - Kessler, Thorsten
AU - Jamshidi, Yalda
AU - van den Berg, Marten E
AU - Kaess, Bernhard
AU - Nelson, Christopher P
AU - Bastiaenen, Rachel
AU - De Bortoli, Marzia
AU - Rossini, Alessandra
AU - Deisenhofer, Isabel
AU - Stark, Klaus
AU - Assa, Solmaz
AU - Braund, Peter S
AU - Cabrera, Claudia
AU - Dominiczak, Anna F
AU - Gögele, Martin
AU - Hall, Leanne M
AU - Ikram, M Arfan
AU - Kavousi, Maryam
AU - Lackner, Karl J
AU - Müller, Christian
AU - Münzel, Thomas
AU - Nauck, Matthias
AU - Padmanabhan, Sandosh
AU - Pfeiffer, Norbert
AU - Spector, Tim D
AU - Uitterlinden, Andre G
AU - Verweij, Niek
AU - Völker, Uwe
AU - Warren, Helen R
AU - Zafar, Mobeen
AU - Felix, Stephan B
AU - Kors, Jan A
AU - Snieder, Harold
AU - Munroe, Patricia B
AU - Pattaro, Cristian
AU - Fuchsberger, Christian
AU - Schmidt, Georg
AU - Nolte, Ilja M
AU - Schunkert, Heribert
AU - Pramstaller, Peter P
AU - Wild, Philipp S
AU - van der Harst, Pim
AU - Stricker, Bruno H
AU - Schnabel, Renate B
AU - Samani, Nilesh J
AU - Hengstenberg, Christian
AU - Dörr, Marcus
AU - Behr, Elijah R
N1 - Publisher Copyright:
Copyright: © 2019, Teumer et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.
PY - 2019/12/5
Y1 - 2019/12/5
N2 - 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.
AB - 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.
KW - Alleles
KW - Death, Sudden, Cardiac
KW - Electrocardiography/methods
KW - Female
KW - Genetic Loci
KW - Genetic Predisposition to Disease/genetics
KW - Genome-Wide Association Study/methods
KW - Genotype
KW - Heart Ventricles
KW - Humans
KW - Male
KW - Polymorphism, Single Nucleotide
KW - Shal Potassium Channels/genetics
KW - Transcriptome
KW - Ventricular Fibrillation/genetics
KW - Whites/genetics
UR - http://www.scopus.com/inward/record.url?scp=85078449379&partnerID=8YFLogxK
U2 - 10.1172/jci.insight.131156
DO - 10.1172/jci.insight.131156
M3 - Article
C2 - 31600170
SN - 2379-3708
VL - 4
JO - JCI Insight
JF - JCI Insight
IS - 23
M1 - e131156
ER -