iScience (Oct 2022)

Genome-wide analyses identify SCN5A as a susceptibility locus for premature atrial contraction frequency

  • Sébastien Thériault,
  • Medea Imboden,
  • Mary L. Biggs,
  • Thomas R. Austin,
  • Stefanie Aeschbacher,
  • Emmanuel Schaffner,
  • Jennifer A. Brody,
  • Traci M. Bartz,
  • Martin Risch,
  • Kirsten Grossmann,
  • Henry J. Lin,
  • Elsayed Z. Soliman,
  • Wendy S. Post,
  • Lorenz Risch,
  • Jose E. Krieger,
  • Alexandre C. Pereira,
  • Susan R. Heckbert,
  • Nona Sotoodehnia,
  • Nicole M. Probst-Hensch,
  • David Conen

Journal volume & issue
Vol. 25, no. 10
p. 105210

Abstract

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Summary: Premature atrial contractions (PACs) are frequently observed on electrocardiograms and are associated with increased risks of atrial fibrillation (AF), stroke, and mortality. In this study, we aimed to identify genetic susceptibility loci for PAC frequency. We performed a genome-wide association study meta-analysis with PAC frequency obtained from ambulatory cardiac monitoring in 4,831 individuals of European ancestry. We identified a genome-wide significant locus at the SCN5A gene. The lead variant, rs7373862, located in an intron of SCN5A, was associated with an increase of 0.12 [95% CI 0.08–0.16] standard deviations of the normalized PAC frequency per risk allele. Among genetic variants previously associated with AF, there was a significant enrichment in concordance of effect for PAC frequency (n = 73/106, p = 5.1 × 10−5). However, several AF risk loci, including PITX2, were not associated with PAC frequency. These findings suggest the existence of both shared and distinct genetic mechanisms for PAC frequency and AF.

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