冠状动脉微血管疾病并发症的范围不断扩大:代谢性疾病及其他

IF 4.9 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Patricia E. McCallinhart , Alejandro R. Chade , Shawn B. Bender , Aaron J. Trask
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引用次数: 0

摘要

冠状动脉微血管病变(CMD)和冠状动脉血流控制受损是心脏代谢疾病心力衰竭发病机制中的早期缺陷,发生在动脉粥样硬化之前。事实上,最近的研究表明,CMD 是肥胖和代谢性疾病患者心脏发病率和死亡率的独立预测因素。CMD 由功能性、结构性和机械性损伤组成,在代谢性疾病和其他并发症(包括移植、自身免疫性疾病、化疗引起的心脏毒性和远端损伤引起的 CMD)中,这些损伤协同作用并最终降低冠状动脉血流量。本综述根据临床前小型和大型动物模型的机理数据,结合现有的临床证据,并考虑到在人体中研究这些机理的局限性,总结了与代谢性和这些其他并发症中的 CMD 相关的最新研究进展。此外,我们还讨论了当前认识中的差距、新出现的关注领域以及该领域未来研究的机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expanding landscape of coronary microvascular disease in co-morbid conditions: Metabolic disease and beyond

Coronary microvascular disease (CMD) and impaired coronary blood flow control are defects that occur early in the pathogenesis of heart failure in cardiometabolic conditions, prior to the onset of atherosclerosis. In fact, recent studies have shown that CMD is an independent predictor of cardiac morbidity and mortality in patients with obesity and metabolic disease. CMD is comprised of functional, structural, and mechanical impairments that synergize and ultimately reduce coronary blood flow in metabolic disease and in other co-morbid conditions, including transplant, autoimmune disorders, chemotherapy-induced cardiotoxicity, and remote injury-induced CMD. This review summarizes the contemporary state-of-the-field related to CMD in metabolic and these other co-morbid conditions based on mechanistic data derived mostly from preclinical small- and large-animal models in light of available clinical evidence and given the limitations of studying these mechanisms in humans. In addition, we also discuss gaps in current understanding, emerging areas of interest, and opportunities for future investigations in this field.

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来源期刊
CiteScore
10.70
自引率
0.00%
发文量
171
审稿时长
42 days
期刊介绍: The Journal of Molecular and Cellular Cardiology publishes work advancing knowledge of the mechanisms responsible for both normal and diseased cardiovascular function. To this end papers are published in all relevant areas. These include (but are not limited to): structural biology; genetics; proteomics; morphology; stem cells; molecular biology; metabolism; biophysics; bioengineering; computational modeling and systems analysis; electrophysiology; pharmacology and physiology. Papers are encouraged with both basic and translational approaches. The journal is directed not only to basic scientists but also to clinical cardiologists who wish to follow the rapidly advancing frontiers of basic knowledge of the heart and circulation.
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