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心房颤动:在了解微小RNA在心房重构中的作用及电生理概述方面的最新进展

Atrial fibrillation: recent advances in understanding the role of microRNAs in atrial remodeling with an electrophysiological overview.

作者信息

Poudel Pradeep, Xu Yanmin, Cui Zhanqian, Sharma Deepak, Tian Bing, Paudel Sudarshan

机构信息

International College of Tianjin Medical University, Tianjin, PR China.

出版信息

Cardiology. 2015;131(1):58-67. doi: 10.1159/000375403. Epub 2015 Apr 8.

Abstract

Atrial fibrillation (AF) is a highly prevalent condition associated with pronounced cardiovascular-related morbidity, mortality and socioeconomic burden. It accounts for more hospitalization days than does any other arrhythmia. This article reviews the basic electrophysiology of AF, electrical and structural remodeling in AF and recent advances in understanding the molecular mechanisms of AF in relation to specific microRNAs. This paper also reviews the potential role of microRNAs as novel therapeutic targets as well as biomarkers in the management of AF. AF shows characteristics typical of altered electrophysiology that promote ectopic activity and facilitate reentry, thereby contributing to the progression from short paroxysmal AF to a persistent, permanent form via atrial remodeling, even in the absence of progressive underlying heart disease. MicroRNAs have been suggested to influence the development of AF by regulating gene expression at the post-transcriptional level. Increasing evidence has identified various microRNA modifications and their impacts on AF initiation and maintenance through electrical and structural remodeling. The discovery of specific microRNAs as novel therapeutic targets and some experimental evidence implicating microRNAs as potential molecular diagnostic markers have had a significant impact on the diagnosis and management of AF and demand further research.

摘要

心房颤动(AF)是一种高度普遍的疾病,与明显的心血管相关发病率、死亡率及社会经济负担相关。它导致的住院天数比其他任何心律失常都多。本文综述了房颤的基本电生理学、房颤中的电重构和结构重构,以及在理解与特定微小RNA相关的房颤分子机制方面的最新进展。本文还综述了微小RNA作为新型治疗靶点以及生物标志物在房颤管理中的潜在作用。房颤表现出典型的电生理学改变特征,这些特征促进异位活动并利于折返,从而即使在没有进行性潜在心脏病的情况下,也可通过心房重构促使房颤从短阵性房颤进展为持续性、永久性房颤。微小RNA被认为可通过在转录后水平调节基因表达来影响房颤的发生发展。越来越多的证据已确定了各种微小RNA修饰及其通过电重构和结构重构对房颤起始和维持的影响。作为新型治疗靶点的特定微小RNA的发现以及一些将微小RNA作为潜在分子诊断标志物的实验证据,对房颤的诊断和管理产生了重大影响,需要进一步研究。

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