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心房颤动的表观遗传机制及治疗意义

Epigenetic Mechanism and Therapeutic Implications of Atrial Fibrillation.

作者信息

Li Dan, Nie Jiali, Han Yu, Ni Li

机构信息

Division of Cardiology, Department of Internal Medicine and Hubei Key Laboratory of Genetics and Molecular Mechanisms of Cardiological Disorders, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Cardiovasc Med. 2022 Jan 21;8:763824. doi: 10.3389/fcvm.2021.763824. eCollection 2021.

Abstract

Atrial fibrillation (AF) is the most common arrhythmia attacking 1. 5-2.0% of general population worldwide. It has a significant impact on morbidity and mortality globally and its prevalence increases exponentially with age. Therapies like catheter ablation or conventional antiarrhythmic drugs have not provided effective solution to the recurrence for AF over the past decades. Over 100 genetic loci have been discovered to be associated with AF by Genome-wide association studies (GWAS) but none has led to a therapy. Recently potential involvement of epigenetics (DNA methylation, histone modification, and non-coding RNAs) in the initiation and maintenance of AF has partly emerged as proof-of-concept in the mechanism and management of AF. Here we reviewed the epigenetic features involved in AF pathophysiology and provided an update of their implications in AF therapy.

摘要

心房颤动(AF)是最常见的心律失常,全球普通人群中1.5%-2.0%的人受其影响。它对全球发病率和死亡率有重大影响,且其患病率随年龄呈指数增长。在过去几十年中,诸如导管消融或传统抗心律失常药物等治疗方法尚未为房颤复发提供有效的解决方案。通过全基因组关联研究(GWAS)已发现100多个与房颤相关的基因位点,但尚无一个能带来治疗方法。最近,表观遗传学(DNA甲基化、组蛋白修饰和非编码RNA)在房颤发生和维持中的潜在作用已部分显现,成为房颤机制和管理方面的概念验证。在此,我们综述了房颤病理生理学中涉及的表观遗传特征,并更新了它们在房颤治疗中的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e77/8815458/e42f12c9a5ec/fcvm-08-763824-g0001.jpg

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