Holmes Jeffrey W, Laksman Zachary, Gepstein Lior
Departments of Biomedical Engineering and Medicine, Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA, United States.
Cardiac Electrophysiology, University of British Columbia, Vancouver, BC, Canada.
Prog Biophys Mol Biol. 2016 Jan;120(1-3):134-48. doi: 10.1016/j.pbiomolbio.2015.11.002. Epub 2015 Nov 23.
Following myocardial infarction (MI), damaged myocytes are replaced by collagenous scar tissue, which serves an important mechanical function - maintaining integrity of the heart wall against enormous mechanical forces - but also disrupts electrical function as structural and electrical remodeling in the infarct and borderzone predispose to re-entry and ventricular tachycardia. Novel emerging regenerative approaches aim to replace this scar tissue with viable myocytes. Yet an alternative strategy of therapeutically modifying selected scar properties may also prove important, and in some cases may offer similar benefits with lower risk or regulatory complexity. Here, we review potential goals for such modifications as well as recent proof-of-concept studies employing specific modifications, including gene therapy to locally increase conduction velocity or prolong the refractory period in and around the infarct scar, and modification of scar anisotropy to improve regional mechanics and pump function. Another advantage of scar modification techniques is that they have applications well beyond MI. In particular, ablation treats electrical abnormalities of the heart by intentionally generating scar to block aberrant conduction pathways. Yet in diseases such as atrial fibrillation (AF) where ablation can be extensive, treating the electrical disorder can significantly impair mechanical function. Creating smaller, denser scars that more effectively block conduction, and choosing the location of those lesions by balancing their electrical and mechanical impacts, could significantly improve outcomes for AF patients. We review some recent advances in this area, including the use of computational models to predict the mechanical effects of specific lesion sets and gene therapy for functional ablation. Overall, emerging techniques for modifying scar properties represents a potentially important set of tools for improving patient outcomes across a range of heart diseases, whether used in place of or as an adjunct to regenerative approaches.
心肌梗死(MI)后,受损的心肌细胞被胶原瘢痕组织替代,该组织发挥着重要的机械功能——维持心脏壁的完整性以抵御巨大的机械力——但也会破坏电功能,因为梗死区和边缘区的结构和电重塑易引发折返和室性心动过速。新出现的再生方法旨在用有活力的心肌细胞替代这种瘢痕组织。然而,治疗性改变特定瘢痕特性的另一种策略可能也很重要,而且在某些情况下可能以较低的风险或监管复杂性提供类似的益处。在此,我们综述了这种改变的潜在目标以及最近采用特定改变的概念验证研究,包括基因治疗以局部提高梗死瘢痕及其周围的传导速度或延长不应期,以及改变瘢痕各向异性以改善区域力学和泵功能。瘢痕修饰技术的另一个优点是其应用远不止于心肌梗死。特别是,消融通过有意形成瘢痕来阻断异常传导通路,从而治疗心脏的电异常。然而,在心房颤动(AF)等疾病中,消融范围可能很大,治疗电紊乱会显著损害机械功能。创建更小、更致密的瘢痕以更有效地阻断传导,并通过平衡其电和机械影响来选择这些病变的位置,可能会显著改善房颤患者的预后。我们综述了该领域的一些最新进展,包括使用计算模型预测特定病变组的机械效应以及用于功能性消融的基因治疗。总体而言,改变瘢痕特性的新兴技术代表了一组潜在的重要工具,可用于改善一系列心脏病患者的预后,无论是替代再生方法还是作为其辅助手段。