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PR间期相关基因、心房重构与心房颤动导管消融的节律转归——基于全基因组关联研究(GWAS)数据的基因分析

PR Interval Associated Genes, Atrial Remodeling and Rhythm Outcome of Catheter Ablation of Atrial Fibrillation-A Gene-Based Analysis of GWAS Data.

作者信息

Husser Daniela, Büttner Petra, Stübner Dorian, Ueberham Laura, Platonov Pyotr G, Dinov Borislav, Arya Arash, Hindricks Gerhard, Bollmann Andreas

机构信息

Department of Electrophysiology, Heart Center Leipzig, Leipzig University, Leipzig, Germany.

Leipzig Heart Institute, Leipzig, Germany.

出版信息

Front Genet. 2017 Dec 19;8:224. doi: 10.3389/fgene.2017.00224. eCollection 2017.

Abstract

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. Samples from 660 patients with paroxysmal ( = 370) or persistent AF ( = 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, , and associated with the PR interval. Of those, and were significantly associated with left atrial low voltage areas and left atrial diameter and subsequently with AF recurrence after radiofrequency catheter ablation. This study suggests contributions of and 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.

摘要

近期研究表明,PR间期延长与晚期左心房重构及导管消融术后房颤(AF)复发相关。尽管不同的全基因组关联研究(GWAS)已发现13个基因位点与作为房颤内表型的PR间期相关,但其随后与房颤重构及导管消融反应的关联尚不清楚。在此,我们对GWAS数据进行基于基因的分析,以检验PR间期候选基因也与房颤导管消融术后左心房重构及心律失常复发相关的假设。对660例接受房颤导管消融的阵发性房颤(n = 370)或持续性房颤(n = 290)患者的样本进行了约100万个单核苷酸多态性(SNP)的基因分型。使用VEGAS(通用基于基因的关联研究)研究基于基因的关联。在13个候选基因中,[基因名称1]、[基因名称2]和[基因名称3]与PR间期相关。其中,[基因名称1]和[基因名称2]与左心房低电压区和左心房直径显著相关,进而与射频导管消融术后房颤复发相关。本研究提示[基因名称1]和[基因名称2]对以PR间期延长、低电压区和左心房扩张表现的房颤重构有影响,进而对导管消融反应有影响。未来需要更大规模的研究来重复和应用这些发现,以期设计基于房颤病理生理学的多位点风险评分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0317/5742186/3f2f3435c661/fgene-08-00224-g0001.jpg

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