Ablatogenomics: can genotype guide catheter ablation for cardiac arrhythmias?

被引:4
|
作者
Roberts, Jason D. [1 ]
Marcus, Gregory M. [2 ]
机构
[1] Western Univ, Dept Med, Sect Cardiac Electrophysiol, Div Cardiol, London, ON N6A 4A5, Canada
[2] Univ Calif San Francisco, Dept Med, Sect Cardiac Electrophysiol, Div Cardiol, San Francisco, CA 94143 USA
关键词
ablatogenomics; arrhythmia; atrial fibrillation; catheter ablation; genetics; personalized medicine; OF-FUNCTION MUTATION; PAROXYSMAL ATRIAL-FIBRILLATION; ANTIARRHYTHMIC-DRUG THERAPY; PULMONARY VEIN ISOLATION; GENOME-WIDE ASSOCIATION; POSTERIOR LEFT ATRIUM; SUPRAVENTRICULAR TACHYCARDIA; GENETIC-POLYMORPHISM; CHROMOSOME; 4Q25; COMMON VARIANTS;
D O I
10.2217/pgs-2016-0114
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Previously confined to the management of rare inherited arrhythmia syndromes, a role for genetics within cardiac electrophysiology has begun to emerge for more common arrhythmias, including atrial fibrillation (AF). Catheter ablation for AF is an invasive procedure effective for restoring normal rhythm, however, fails in up to 40% of those undergoing their first procedure and carries a risk for serious adverse events. Recent studies have suggested that a common genetic variant within chromosome 4q25 may be a powerful predictor of procedural success, highlighting the potential of an 'ablatogenomic' strategy. Although still in its infancy, an ablatogenomic approach for AF may facilitate delivery of ablation to those most likely to benefit, while sparing those prone to fail from its risks.
引用
收藏
页码:1931 / 1940
页数:10
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