Hunter Wynn G, Kelly Jacob P, McGarrah Robert W, Kraus William E, Shah Svati H
Duke University School of Medicine, 300 North Duke Street, Durham, NC, 27701, USA.
Division of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Curr Heart Fail Rep. 2016 Jun;13(3):119-31. doi: 10.1007/s11897-016-0289-5.
Metabolic impairment is an intrinsic component of heart failure (HF) pathophysiology. Although initially conceived as a myocardial defect, metabolic dysfunction is now recognized as a systemic process with complex interplay between the myocardium and peripheral tissues and organs. Specifically, HF-associated metabolic dysfunction includes alterations in substrate utilization, insulin resistance, defects in energy production, and imbalanced anabolic-catabolic signaling leading to cachexia. Each of these metabolic abnormalities is associated with significant morbidity and mortality in patients with HF; however, their detection and therapeutic management remains challenging. Given the difficulty in obtaining human cardiac tissue for research purposes, peripheral blood metabolomic profiling, a well-established approach for characterizing small-molecule metabolite intermediates from canonical biochemical pathways, may be a useful technology for dissecting biomarkers and mechanisms of metabolic impairment in HF. In this review, metabolic abnormalities in HF will be discussed with particular emphasis on the application of metabolomic profiling to detecting, risk stratifying, and identifying novel targets for metabolic therapy in this heterogeneous population.
代谢功能障碍是心力衰竭(HF)病理生理学的一个内在组成部分。尽管最初被认为是心肌缺陷,但现在代谢功能障碍被认为是一个全身性过程,心肌与外周组织和器官之间存在复杂的相互作用。具体而言,与HF相关的代谢功能障碍包括底物利用改变、胰岛素抵抗、能量产生缺陷以及导致恶病质的合成代谢-分解代谢信号失衡。这些代谢异常中的每一种都与HF患者的高发病率和死亡率相关;然而,对它们的检测和治疗管理仍然具有挑战性。鉴于获取用于研究目的的人体心脏组织存在困难,外周血代谢组学分析是一种用于表征经典生化途径中小分子代谢物中间体的成熟方法,可能是剖析HF中代谢功能障碍的生物标志物和机制的有用技术。在这篇综述中,将讨论HF中的代谢异常,特别强调代谢组学分析在检测、风险分层以及识别这一异质性人群中代谢治疗新靶点方面的应用。