Chromosome 4q25 Variants Have Less Co-Morbid Risk Factors and High Left Atrial Conduction Velocity in Korean Patients Who Underwent Radiofrequency Catheter Ablation of Atrial Fibrillation

Jaemin Shim, Hui Nam Pak, Hye Jin Hwang, Jong Youn Kim, Boyoung Joung, Moon Hyoung Lee, Yangsoo Jang

Research output: Contribution to journalArticle

Abstract

Background: Recent studies have demonstrated the association of 4q25 gene single nucleotide polymorphism (SNP) with atrial fibrillation (AF). We evaluated potential relationships of 4 SNPs on chromosome 4q25 with clinical and electrophysiological characteristics in patients undergoing Catheter ablation for AF. Methods: A total of 295 consecutive patients (56 ± 11 years, 78% male) with paroxysmal (68.7%) or persistent (31.3%) AF were included. Genotyping for 4 SNPs in close proximity to PITX2 gene on chromosome 4q25 (rs2200733, rs10033464, rs17042171, and rs6843082) were performed and compared with clinical, electrophysiological, and imaging database. Results: There were no significant differences in clinical and electrophysiological parameters between major and minor allele group of rs10033464, rs17042171, and rs6843082. In contrast, rs2200733 variant was associated with lower CHADS score (0.73±0.95 vs. 1.17± 1.10, p=0.021), lower prevalence of heart failure (2.5 vs. 11.5%, p=0.023), hypertension (42.3 vs. 68.9%, p=0.006), and patients with age>75 (1.2 vs 6.9%, p=0.030). In electrophysiological study, conduction velocity of left atrium was significantly higher (0.67±0.35 m/s vs. 0.55±0.22 m/s, p=0.042) in patients with variant allele of rs2200733. Conclusions: In Korean population, rs2200733 at 4q25 was the only significant SNPs associated with clinical and electrophysiological trait. It may increase the risk of AF without traditional risk factors and significant electroanatomical remodeling.

Original languageEnglish
Number of pages1
JournalJournal of Arrhythmia
Volume27
Issue number4
DOIs
Publication statusPublished - 2011 Jan 1
Externally publishedYes

Fingerprint

Catheter Ablation
Atrial Fibrillation
Single Nucleotide Polymorphism
Chromosomes
Alleles
Heart Atria
Genes
Heart Failure
Databases
Hypertension
Population

Keywords

  • atrial fibrillation
  • Catheter ablation
  • single nucleotide polymorphism

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

Chromosome 4q25 Variants Have Less Co-Morbid Risk Factors and High Left Atrial Conduction Velocity in Korean Patients Who Underwent Radiofrequency Catheter Ablation of Atrial Fibrillation. / Shim, Jaemin; Pak, Hui Nam; Hwang, Hye Jin; Kim, Jong Youn; Joung, Boyoung; Lee, Moon Hyoung; Jang, Yangsoo.

In: Journal of Arrhythmia, Vol. 27, No. 4, 01.01.2011.

Research output: Contribution to journalArticle

@article{275e2573c9284116a841bd87b90dccb7,
title = "Chromosome 4q25 Variants Have Less Co-Morbid Risk Factors and High Left Atrial Conduction Velocity in Korean Patients Who Underwent Radiofrequency Catheter Ablation of Atrial Fibrillation",
abstract = "Background: Recent studies have demonstrated the association of 4q25 gene single nucleotide polymorphism (SNP) with atrial fibrillation (AF). We evaluated potential relationships of 4 SNPs on chromosome 4q25 with clinical and electrophysiological characteristics in patients undergoing Catheter ablation for AF. Methods: A total of 295 consecutive patients (56 ± 11 years, 78{\%} male) with paroxysmal (68.7{\%}) or persistent (31.3{\%}) AF were included. Genotyping for 4 SNPs in close proximity to PITX2 gene on chromosome 4q25 (rs2200733, rs10033464, rs17042171, and rs6843082) were performed and compared with clinical, electrophysiological, and imaging database. Results: There were no significant differences in clinical and electrophysiological parameters between major and minor allele group of rs10033464, rs17042171, and rs6843082. In contrast, rs2200733 variant was associated with lower CHADS score (0.73±0.95 vs. 1.17± 1.10, p=0.021), lower prevalence of heart failure (2.5 vs. 11.5{\%}, p=0.023), hypertension (42.3 vs. 68.9{\%}, p=0.006), and patients with age>75 (1.2 vs 6.9{\%}, p=0.030). In electrophysiological study, conduction velocity of left atrium was significantly higher (0.67±0.35 m/s vs. 0.55±0.22 m/s, p=0.042) in patients with variant allele of rs2200733. Conclusions: In Korean population, rs2200733 at 4q25 was the only significant SNPs associated with clinical and electrophysiological trait. It may increase the risk of AF without traditional risk factors and significant electroanatomical remodeling.",
keywords = "atrial fibrillation, Catheter ablation, single nucleotide polymorphism",
author = "Jaemin Shim and Pak, {Hui Nam} and Hwang, {Hye Jin} and Kim, {Jong Youn} and Boyoung Joung and Lee, {Moon Hyoung} and Yangsoo Jang",
year = "2011",
month = "1",
day = "1",
doi = "10.4020/jhrs.27.OP59_1",
language = "English",
volume = "27",
journal = "Journal of Arrhythmia",
issn = "1880-4276",
publisher = "Elsevier BV",
number = "4",

}

TY - JOUR

T1 - Chromosome 4q25 Variants Have Less Co-Morbid Risk Factors and High Left Atrial Conduction Velocity in Korean Patients Who Underwent Radiofrequency Catheter Ablation of Atrial Fibrillation

AU - Shim, Jaemin

AU - Pak, Hui Nam

AU - Hwang, Hye Jin

AU - Kim, Jong Youn

AU - Joung, Boyoung

AU - Lee, Moon Hyoung

AU - Jang, Yangsoo

PY - 2011/1/1

Y1 - 2011/1/1

N2 - Background: Recent studies have demonstrated the association of 4q25 gene single nucleotide polymorphism (SNP) with atrial fibrillation (AF). We evaluated potential relationships of 4 SNPs on chromosome 4q25 with clinical and electrophysiological characteristics in patients undergoing Catheter ablation for AF. Methods: A total of 295 consecutive patients (56 ± 11 years, 78% male) with paroxysmal (68.7%) or persistent (31.3%) AF were included. Genotyping for 4 SNPs in close proximity to PITX2 gene on chromosome 4q25 (rs2200733, rs10033464, rs17042171, and rs6843082) were performed and compared with clinical, electrophysiological, and imaging database. Results: There were no significant differences in clinical and electrophysiological parameters between major and minor allele group of rs10033464, rs17042171, and rs6843082. In contrast, rs2200733 variant was associated with lower CHADS score (0.73±0.95 vs. 1.17± 1.10, p=0.021), lower prevalence of heart failure (2.5 vs. 11.5%, p=0.023), hypertension (42.3 vs. 68.9%, p=0.006), and patients with age>75 (1.2 vs 6.9%, p=0.030). In electrophysiological study, conduction velocity of left atrium was significantly higher (0.67±0.35 m/s vs. 0.55±0.22 m/s, p=0.042) in patients with variant allele of rs2200733. Conclusions: In Korean population, rs2200733 at 4q25 was the only significant SNPs associated with clinical and electrophysiological trait. It may increase the risk of AF without traditional risk factors and significant electroanatomical remodeling.

AB - Background: Recent studies have demonstrated the association of 4q25 gene single nucleotide polymorphism (SNP) with atrial fibrillation (AF). We evaluated potential relationships of 4 SNPs on chromosome 4q25 with clinical and electrophysiological characteristics in patients undergoing Catheter ablation for AF. Methods: A total of 295 consecutive patients (56 ± 11 years, 78% male) with paroxysmal (68.7%) or persistent (31.3%) AF were included. Genotyping for 4 SNPs in close proximity to PITX2 gene on chromosome 4q25 (rs2200733, rs10033464, rs17042171, and rs6843082) were performed and compared with clinical, electrophysiological, and imaging database. Results: There were no significant differences in clinical and electrophysiological parameters between major and minor allele group of rs10033464, rs17042171, and rs6843082. In contrast, rs2200733 variant was associated with lower CHADS score (0.73±0.95 vs. 1.17± 1.10, p=0.021), lower prevalence of heart failure (2.5 vs. 11.5%, p=0.023), hypertension (42.3 vs. 68.9%, p=0.006), and patients with age>75 (1.2 vs 6.9%, p=0.030). In electrophysiological study, conduction velocity of left atrium was significantly higher (0.67±0.35 m/s vs. 0.55±0.22 m/s, p=0.042) in patients with variant allele of rs2200733. Conclusions: In Korean population, rs2200733 at 4q25 was the only significant SNPs associated with clinical and electrophysiological trait. It may increase the risk of AF without traditional risk factors and significant electroanatomical remodeling.

KW - atrial fibrillation

KW - Catheter ablation

KW - single nucleotide polymorphism

UR - http://www.scopus.com/inward/record.url?scp=85009585810&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85009585810&partnerID=8YFLogxK

U2 - 10.4020/jhrs.27.OP59_1

DO - 10.4020/jhrs.27.OP59_1

M3 - Article

AN - SCOPUS:85009585810

VL - 27

JO - Journal of Arrhythmia

JF - Journal of Arrhythmia

SN - 1880-4276

IS - 4

ER -