Key result
An ablatogenomic strategy using genetic variants like chromosome 4q25 may predict procedural success for atrial fibrillation ablation, which currently fails in up to 40% of first procedures.
Why the study?
Does a genotype-guided strategy (ablatogenomics) improve patient selection and outcomes for catheter ablation in atrial fibrillation?
Does a genotype-guided strategy (ablatogenomics) improve patient selection and outcomes for catheter ablation in atrial fibrillation?
An ablatogenomic approach using genetic variants like chromosome 4q25 may help identify patients most likely to benefit from AF ablation, sparing others from procedural risks.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for ablatogenomics in AF ablation; prospective trials needed before clinical adoption.
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.
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Roberts et al. (2016) conducted a review in Atrial fibrillation. Ablatogenomic strategy was evaluated. An ablatogenomic strategy using genetic variants like chromosome 4q25 may predict procedural success for atrial fibrillation ablation, which currently fails in up to 40% of first procedures.
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