Department of Anaesthesiology, Intensive Care, Emergency and Pain Medicine, University of Würzburg, 97080 Würzburg, Germany.
Institute for Transfusion Medicine, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany.
Int J Mol Sci. 2024 Apr 25;25(9):4689. doi: 10.3390/ijms25094689.
In atrial fibrillation (AF), multifactorial pathologic atrial alterations are manifested by structural and electrophysiological changes known as atrial remodeling. AF frequently develops in the context of underlying cardiac abnormalities. A critical mechanistic role played by atrial stretch is played by abnormal substrates in a number of conditions that predispose to AF, including obesity, heart failure, hypertension, and sleep apnea. The significant role of overweight and obesity in the development of AF is known; however, the differential effect of overweight, obesity, cardiovascular comorbidities, lifestyle, and other modifiable risk factors on the occurrence and recurrence of AF remains to be determined. Reverse remodeling of the atrial substrate and subsequent reduction in the AF burden by conversion into a typical sinus rhythm has been associated with weight loss through lifestyle changes or surgery. This makes it an essential pillar in the management of AF in obese patients. According to recently published research, microRNAs (miRs) may function as post-transcriptional regulators of genes involved in atrial remodeling, potentially contributing to the pathophysiology of AF. The focus of this review is on their modulation by both weight loss and catheter ablation interventions to counteract atrial remodeling in AF. Our analysis outlines the experimental and clinical evidence supporting the synergistic effects of weight loss and catheter ablation (CA) in reversing atrial electrical and structural remodeling in AF onset and in recurrent post-ablation AF by attenuating pro-thrombotic, pro-inflammatory, pro-fibrotic, arrhythmogenic, and male-sex-associated hypertrophic remodeling pathways. Furthermore, we discuss the promising role of miRs with prognostic potential as predictive biomarkers in guiding approaches to AF recurrence prevention.
在心房颤动(AF)中,多种病理心房改变表现为结构和电生理变化,称为心房重构。AF 常发生于潜在的心脏异常。在许多易发生 AF 的情况下,心房拉伸的异常基质起着关键的机械作用,这些情况包括肥胖、心力衰竭、高血压和睡眠呼吸暂停。超重和肥胖在 AF 发展中的重要作用是已知的;然而,超重、肥胖、心血管合并症、生活方式和其他可改变的危险因素对 AF 的发生和复发的差异影响仍有待确定。通过生活方式改变或手术减肥,心房基质的逆向重构以及随后将 AF 负荷减少为典型窦性节律,与体重减轻有关。这使其成为肥胖患者 AF 管理的重要支柱。根据最近发表的研究,微小 RNA(miRs)可能作为参与心房重构的基因的转录后调节剂发挥作用,可能有助于 AF 的病理生理学。本综述的重点是它们在体重减轻和导管消融干预下的调节作用,以抵消 AF 中的心房电和结构重构。我们的分析概述了支持体重减轻和导管消融(CA)协同作用的实验和临床证据,通过减轻促血栓形成、促炎、促纤维化、致心律失常和男性相关肥大重构途径,在 AF 发作和复发性消融后 AF 中逆转心房电和结构重构。此外,我们讨论了具有预后潜力的 miRs 作为预测生物标志物在指导 AF 复发预防方法中的有前途的作用。