Gevaert Andreas B, Lemmens Katrien, Vrints Christiaan J, Van Craenenbroeck Emeline M
Department of Translational Pathophysiological Research and Research Group Cardiovascular Diseases, University of Antwerp, Antwerp, Belgium.
Laboratory of Cellular and Molecular Cardiology and Department of Cardiology, Antwerp University Hospital (UZA), Edegem, Belgium.
Oxid Med Cell Longev. 2017;2017:4865756. doi: 10.1155/2017/4865756. Epub 2017 Jun 19.
Although the burden of heart failure with preserved ejection fraction (HFpEF) is increasing, there is no therapy available that improves prognosis. Clinical trials using beta blockers and angiotensin converting enzyme inhibitors, cardiac-targeting drugs that reduce mortality in heart failure with reduced ejection fraction (HFrEF), have had disappointing results in HFpEF patients. A new "whole-systems" approach has been proposed for designing future HFpEF therapies, moving focus from the cardiomyocyte to the endothelium. Indeed, dysfunction of endothelial cells throughout the entire cardiovascular system is suggested as a central mechanism in HFpEF pathophysiology. The objective of this review is to provide an overview of current knowledge regarding endothelial dysfunction in HFpEF. We discuss the molecular and cellular mechanisms leading to endothelial dysfunction and the extent, presence, and prognostic importance of clinical endothelial dysfunction in different vascular beds. We also consider implications towards exercise training, a promising therapy targeting system-wide endothelial dysfunction in HFpEF.
尽管射血分数保留的心力衰竭(HFpEF)负担日益加重,但目前尚无改善预后的治疗方法。使用β受体阻滞剂和血管紧张素转换酶抑制剂(这些药物可降低射血分数降低的心力衰竭(HFrEF)患者的死亡率)的临床试验在HFpEF患者中取得的结果令人失望。有人提出了一种新的“全系统”方法来设计未来的HFpEF治疗方案,将关注点从心肌细胞转向内皮细胞。事实上,整个心血管系统内皮细胞功能障碍被认为是HFpEF病理生理学的核心机制。本综述的目的是概述目前关于HFpEF内皮功能障碍的知识。我们讨论了导致内皮功能障碍的分子和细胞机制,以及不同血管床中临床内皮功能障碍的程度、存在情况和预后重要性。我们还考虑了运动训练的意义,运动训练是一种有前景的针对HFpEF全系统内皮功能障碍的治疗方法。