A self-reinforcing cycle hypothesis in heart failure pathogenesis

IF 9.4 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Carlos Fernandez-Patron, Gary D. Lopaschuk, Eugenio Hardy
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引用次数: 0

Abstract

Heart failure is a progressive syndrome with high morbidity and mortality rates. Here, we suggest that chronic exposure of the heart to risk factors for heart failure damages heart mitochondria, thereby impairing energy production to levels that can suppress the heart’s ability to pump blood and repair mitochondria (both energy-consuming processes). As damaged mitochondria accumulate, the heart becomes deprived of energy in a ‘self-reinforcing cycle’, which can persist after the heart is no longer chronically exposed to (or after antagonism of) the risk factors that initiated the cycle. Together with other previously described pathological mechanisms, this proposed cycle can help explain (1) why heart failure progresses, (2) why it can recur after cessation of treatment, and (3) why heart failure is often accompanied by dysfunction of multiple organs. Ideally, therapy of heart failure syndrome would be best attempted before the self-reinforcing cycle is triggered or designed to break the self-reinforcing cycle. Fernandez-Patron et al. propose a unifying framework explaining how diverse risk factors such as hypertension, obesity and diabetes lead pathogenesis and progression of heart failure.

Abstract Image

心力衰竭发病机制中的自我强化循环假说
心力衰竭是一种进展性综合征,发病率和死亡率都很高。在此,我们认为,心脏长期暴露于心衰的危险因素中会损害心脏线粒体,从而影响能量的产生,使心脏泵血和修复线粒体(这两个过程都需要消耗能量)的能力受到抑制。随着受损线粒体的积累,心脏在 "自我强化循环 "中变得缺乏能量,当心脏不再长期暴露于(或拮抗了)启动该循环的风险因素后,该循环仍会持续。这一循环与之前描述的其他病理机制一起,有助于解释:(1)为什么心力衰竭会发展;(2)为什么心力衰竭会在停止治疗后复发;以及(3)为什么心力衰竭常常伴有多个器官的功能障碍。理想情况下,心衰综合征的治疗最好在自我强化循环触发之前尝试,或旨在打破自我强化循环。Fernandez-Patron 等人提出了一个统一的框架,解释了高血压、肥胖和糖尿病等各种风险因素如何导致心衰的发病和发展。
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来源期刊
CiteScore
5.70
自引率
0.00%
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