4.7 Review

Genetics of atrial fibrillation-practical applications for clinical management: if not now, when and how?

期刊

CARDIOVASCULAR RESEARCH
卷 117, 期 7, 页码 1718-1731

出版社

OXFORD UNIV PRESS
DOI: 10.1093/cvr/cvab153

关键词

Atrial fibrillation; Antiarrhythmic drugs; Catheter ablation; Response; Arrhythmias; Genetic variation; Genotype

资金

  1. National Institutes of Health (NIH) [R01 HL138737, T32 HL139439, 1R01 HL150586]
  2. European Research Council (ERC) under the European Union [648131]
  3. European Union [847770]
  4. German Center for Cardiovascular Research (DZHK e.V.) [81Z1710103]
  5. German Ministry of Research and Education [BMBF 01ZX1408A]
  6. ERACoSysMed3 [031L0239]
  7. British Heart Foundation [FS/13/43/30324, PG/17/30/32961, PG/20/22/35093]
  8. German Centre for Cardiovascular Research by German Ministry of Education and Research (DZHK)
  9. Leducq Foundation
  10. European Union
  11. British Heart Foundation
  12. Medical Research Council (UK)
  13. German Centre for Cardiovascular Research
  14. European Union BigData@Heart [EU IMI 116074]

向作者/读者索取更多资源

The prevalence and economic burden of atrial fibrillation (AF) are expected to more than double in the next few decades. Response to rhythm control therapy for AF varies greatly among individual patients, highlighting the need for better prediction of treatment outcomes.
The prevalence and economic burden of atrial fibrillation (AF) are predicted to more than double over the next few decades. In addition to anticoagulation and treatment of concomitant cardiovascular conditions, early and standardized rhythm control therapy reduces cardiovascular outcomes as compared with a rate control approach, favouring the restoration, and maintenance of sinus rhythm safely. Current therapies for rhythm control of AF include antiarrhythmic drugs (AADs) and catheter ablation (CA). However, response in an individual patient is highly variable with some remaining free of AF for long periods on antiarrhythmic therapy, while others require repeat AF ablation within weeks. The limited success of rhythm control therapy for AF is in part related to incomplete understanding of the pathophysiological mechanisms and our inability to predict responses in individual patients. Thus, a major knowledge gap is predicting which patients with AF are likely to respond to rhythm control approach. Over the last decade, tremendous progress has been made in defining the genetic architecture of AF with the identification of rare mutations in cardiac ion channels, signalling molecules, and myocardial structural proteins associated with familial (early-onset) AF. Conversely, genome-wide association studies have identified common variants at over 100 genetic loci and the development of polygenic risk scores has identified high-risk individuals. Although retrospective studies suggest that response to AADs and CA is modulated in part by common genetic variation, the development of a comprehensive clinical and genetic risk score may enable the translation of genetic data to the bedside care of AF patients. Given the economic impact of the AF epidemic, even small changes in therapeutic efficacy may lead to substantial improvements for patients and health care systems. [GRAPHICS] .

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据