Abstract

Atrial fibrillation (AF) is a highly prevalent cardiac arrhythmia disease, which widely leads to exacerbate heart failure and ischemic stroke in elder world. Recently, long non-coding RNAs (lncRNAs), a subclass of noncoding RNAs, have been reported to play critical roles in pathophysiology of cardiac heart. However, little is known of their role in cardiac arrhythmia. In the present study, we investigated the expression levels of lncRNAs of AF patients and healthy people with Agilent Human lncRNA array for the first time. 177 lncRNAs of 78243 and 153 mRNAs of 30215 tested were identified to be differentially expressed (≥ 2-fold change), indicating that the expression of many lncRNAs are upregulated or downregulated in AF. Among these, NONHSAT040387 and NONHSAT098586 were the most upregulated and downregulated lncRNAs. Real time quantitative PCR were employed to validate the microarray analysis findings, and the results confirmed the consistence. GO and KEGG pathway analysis were applied to explore the potential lncRNAs functions, some pathways including oxygen transporter activity and protein heterodimerization activity were speculated to be involved in AF pathogenesis. These results shed some light on lncRNAs' physiologic functions and provide useful information for exploring potential therapeutic treatments for heart rhythm disease.

Highlights

  • Atrial fibrillation (AF) is the most common heart rhythm disease in the world, accounting approximately 0.5% of the total world population [1, 2]

  • LncRNA profiling showed 177 long non-coding RNAs (lncRNAs) of 78243 tested with significant differential expression levels at least a two-fold change in AF patients compared with normal patients, with 100 up-regulated and 77 down-regulated, respectively

  • This study was designed to discover the relationship between lncRNAs expression and atrial structural remodeling of AF

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Summary

Introduction

Atrial fibrillation (AF) is the most common heart rhythm disease in the world, accounting approximately 0.5% of the total world population [1, 2]. A higher incidence of adverse consequences for the elderly has been associated with atrial fibrillation. The precise mechanisms of atrial remodeling were not well elucidated, leading to the demand of investigating the exact mechanisms of the disease and developing treatments. The ncRNAs include microRNAs (miRNAs), PIWI interacting RNAs, and endogenous small interfering RNAs. the notion of ncRNAs acting as heart disease modulators is not new; reviews regarding the role of ncRNAs in heart disease have already been published before [6]. LncRNAs may function through a variety of mechanisms such as modulating gene transcription by rearranging chromosomal looping and transcription factor binding.

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