Center for Cardiovascular Research, The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, United States of America.
Department of Medical Pharmacology and Physiology, University of Missouri School of Medicine, Columbia, MO, United States of America; Department of Medicine, University of Missouri School of Medicine, Columbia, MO, United States of America.
J Mol Cell Cardiol. 2024 Jul;192:26-35. doi: 10.1016/j.yjmcc.2024.05.004. Epub 2024 May 10.
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.
冠状动脉微血管疾病(CMD)和受损的冠状动脉血流控制是代谢性心脏疾病中心力衰竭发病机制早期出现的缺陷,早于动脉粥样硬化的发生。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子。CMD 由功能、结构和机械损伤组成,这些损伤协同作用,最终会降低代谢性疾病和其他合并症(包括移植、自身免疫性疾病、化疗诱导的心脏毒性和远程损伤诱导的 CMD)中的冠状动脉血流量。鉴于可用的临床证据,并考虑到在人体中研究这些机制的局限性,本文根据主要来源于临床前小动物和大动物模型的机制数据,综述了代谢和其他合并症中 CMD 的最新研究现状。此外,我们还讨论了目前认识中的差距、该领域新兴的研究兴趣和未来研究的机会。