Abstract

Background: PR interval prolongation has recently been shown to associate with advanced left atrial remodeling and atrial fibrillation (AF) recurrence after catheter ablation. While different genome-wide association studies (GWAS) have implicated 13 loci to associate with the PR interval as an AF endophenotype their subsequent associations with AF remodeling and response to catheter ablation are unknown. Here, we perform a gene-based analysis of GWAS data to test the hypothesis that PR interval candidate genes also associate with left atrial remodeling and arrhythmia recurrence following AF catheter ablation.Methods and Results: Samples from 660 patients with paroxysmal (n = 370) or persistent AF (n = 290) undergoing AF catheter ablation were genotyped for ~1,000,000 SNPs. Gene-based association was investigated using VEGAS (versatile gene-based association study). Among the 13 candidate genes, SLC8A1, MEIS1, ITGA9, SCN5A, and SOX5 associated with the PR interval. Of those, ITGA9 and SOX5 were significantly associated with left atrial low voltage areas and left atrial diameter and subsequently with AF recurrence after radiofrequency catheter ablation.Conclusion: This study suggests contributions of ITGA9 and SOX5 to AF remodeling expressed as PR interval prolongation, low voltage areas and left atrial dilatation and subsequently to response to catheter ablation. Future and larger studies are necessary to replicate and apply these findings with the aim of designing AF pathophysiology-based multi-locus risk scores.

Highlights

  • PR interval prolongation has recently been shown to associate with advanced left atrial remodeling expressed by left atrial (LA) dilatation and reduced LA voltage as well as atrial fibrillation (AF) recurrence after catheter ablation (Park et al, 2014)

  • PR interval was available in 209 patients and measured 180 ± 31 ms

  • Among 13 PR interval candidate genes, SLC8A1, MEIS1, ITGA9, SCN5A, and SOX5 associated with the PR interval

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Summary

Introduction

PR interval prolongation has recently been shown to associate with advanced left atrial remodeling expressed by left atrial (LA) dilatation and reduced LA voltage as well as atrial fibrillation (AF) recurrence after catheter ablation (Park et al, 2014). While different genome-wide association studies (GWAS) have implicated 13 loci to associate with the PR interval as an AF endophenotype (Holm et al, 2010; Pfeufer et al, 2010; Butler et al, 2012; Sano et al, 2014) their subsequent associations with electroanatomical remodeling and response to catheter ablation are unknown. While different genome-wide association studies (GWAS) have implicated 13 loci to associate with the PR interval as an AF endophenotype their subsequent associations with AF remodeling and response to catheter ablation are unknown. We perform a gene-based analysis of GWAS data to test the hypothesis that PR interval candidate genes associate with left atrial remodeling and arrhythmia recurrence following AF catheter ablation

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