微小 RNA 在心房颤动中的作用:从表达特征到功能意义。

MicroRNAs in Atrial Fibrillation: from Expression Signatures to Functional Implications.

机构信息

Department of Cardiology, Heart Center, Academic Medical Center/University of Amsterdam, Amsterdam, The Netherlands.

Department of Experimental Cardiology, Heart Center, Academic Medical Center/University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Cardiovasc Drugs Ther. 2017 Jun;31(3):345-365. doi: 10.1007/s10557-017-6736-z.

Abstract

Atrial fibrillation (AF) is the most common sustained arrhythmia and is associated with pronounced morbidity and mortality. Its prevalence, expected to further increase for the forthcoming years, and associated frequent hospitalizations turn AF into a major health problem. Structural and electrical atrial remodelling underlie the substrate for AF, but the exact mechanisms driving this remodelling remain incompletely understood. Recent studies have shown that microRNAs (miRNA), short non-coding RNAs that regulate gene expression, may be involved in the pathophysiology of AF. MiRNAs have been implicated in AF-induced ion channel remodelling and fibrosis. MiRNAs could therefore provide insight into AF pathophysiology or become novel targets for therapy with miRNA mimics or anti-miRNAs. Moreover, circulating miRNAs have been suggested as a new class of diagnostic and prognostic biomarkers of AF. However, the origin and function of miRNAs in tissue and plasma frequently remain unknown and studies investigating the role of miRNAs in AF vary in design and focus and even present contradicting results. Here, we provide a systematic review of the available clinical and functional studies investigating the tissue and plasma miRNAs in AF and will thereafter discuss the potential of miRNAs as biomarkers or novel therapeutic targets in AF.

摘要

心房颤动(AF)是最常见的持续性心律失常,与明显的发病率和死亡率相关。预计未来几年其患病率将进一步增加,频繁住院使 AF 成为一个主要的健康问题。AF 的发生基础是心房的结构和电重构,但驱动这种重构的确切机制仍不完全清楚。最近的研究表明,微小 RNA(miRNA),一种调节基因表达的短非编码 RNA,可能与 AF 的病理生理学有关。miRNA 已被牵涉到 AF 诱导的离子通道重构和纤维化中。因此,miRNA 可以提供对 AF 病理生理学的深入了解,或者成为 miRNA 模拟物或抗 miRNA 的新型治疗靶点。此外,循环 miRNA 已被提议作为 AF 的一种新的诊断和预后生物标志物。然而,组织和血浆中 miRNA 的来源和功能通常仍不清楚,并且研究 miRNA 在 AF 中的作用的设计和重点各不相同,甚至得出相互矛盾的结果。在这里,我们对现有的研究心房颤动组织和血浆 miRNA 的临床和功能研究进行了系统综述,并将随后讨论 miRNA 作为 AF 生物标志物或新型治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01b9/5550535/9f2c628839cb/10557_2017_6736_Fig1_HTML.jpg

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