Lees Jarmon G, Napierala Marek, Pébay Alice, Dottori Mirella, Lim Shiang Y
O'Brien Institute Department, St Vincent's Institute of Medical Research, Fitzroy, Victoria 3065, Australia; Department of Medicine, The University of Melbourne, Parkville, Victoria 3010, Australia.
Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Int J Cardiol. 2022 Jan 1;346:71-78. doi: 10.1016/j.ijcard.2021.11.033. Epub 2021 Nov 16.
Friedreich's ataxia (FRDA) is a hereditary neuromuscular disorder. Cardiomyopathy is the leading cause of premature death in FRDA. FRDA cardiomyopathy is a complex and progressive disease with no cure or treatment to slow its progression. At the cellular level, cardiomyocyte hypertrophy, apoptosis and fibrosis contribute to the cardiac pathology. However, the heart is composed of multiple cell types and several clinical studies have reported the involvement of cardiac non-myocytes such as vascular cells, autonomic neurons, and inflammatory cells in the pathogenesis of FRDA cardiomyopathy. In fact, several of the cardiac pathologies associated with FRDA including cardiomyocyte necrosis, fibrosis, and arrhythmia, could be contributed to by a diseased vasculature and autonomic dysfunction. Here, we review available evidence regarding the current understanding of cellular mechanisms for, and the involvement of, cardiac non-myocytes in the pathogenesis of FRDA cardiomyopathy.
弗里德赖希共济失调(FRDA)是一种遗传性神经肌肉疾病。心肌病是FRDA患者过早死亡的主要原因。FRDA心肌病是一种复杂的进行性疾病,目前尚无治愈方法或治疗手段能减缓其进展。在细胞水平上,心肌细胞肥大、凋亡和纤维化是导致心脏病变的原因。然而,心脏由多种细胞类型组成,多项临床研究报告称,血管细胞、自主神经和炎症细胞等心脏非心肌细胞参与了FRDA心肌病的发病机制。事实上,与FRDA相关的几种心脏病变,包括心肌细胞坏死、纤维化和心律失常,可能是由病变的脉管系统和自主神经功能障碍导致的。在此,我们综述了有关目前对FRDA心肌病发病机制中心脏非心肌细胞的细胞机制及参与情况的现有证据。