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心力衰竭中的肠促胰岛素相关药物治疗。

Incretin-related drug therapy in heart failure.

作者信息

Vest Amanda R

机构信息

Division of Cardiology, Tufts Medical Center, 800 Washington Street, South 6138, Boston, MA, 02111, USA,

出版信息

Curr Heart Fail Rep. 2015 Feb;12(1):24-32. doi: 10.1007/s11897-014-0232-6.

Abstract

The new pharmacological classes of GLP-1 agonists and DPP-4 inhibitors are now widely used in diabetes and have been postulated as beneficial in heart failure. These proposed benefits arise from the inter-related pathophysiologies of diabetes and heart failure (diabetes increases the risk of heart failure, and heart failure can induce insulin resistance) and also in light of the dysfunctional myocardial energetics seen in heart failure. The normal heart utilizes predominantly fatty acids for energy production, but there is some evidence to suggest that increased myocardial glucose uptake may be beneficial for the failing heart. Thus, GLP-1 agonists, which stimulate glucose-dependent insulin release and enhance myocardial glucose uptake, have become a focus of investigation in both animal models and humans with heart failure. Limited pilot data for GLP-1 agonists shows potential improvements in systolic function, hemodynamics, and quality of life, forming the basis for current phase II trials.

摘要

胰高血糖素样肽-1(GLP-1)受体激动剂和二肽基肽酶-4(DPP-4)抑制剂这两类新型药物目前在糖尿病治疗中广泛应用,并且据推测对心力衰竭有益。这些潜在益处源于糖尿病与心力衰竭相互关联的病理生理学机制(糖尿病会增加心力衰竭风险,而心力衰竭可诱发胰岛素抵抗),同时也鉴于心力衰竭时心肌能量代谢功能失调。正常心脏主要利用脂肪酸产生能量,但有证据表明,增加心肌对葡萄糖的摄取可能对衰竭心脏有益。因此,刺激葡萄糖依赖性胰岛素释放并增强心肌葡萄糖摄取的GLP-1受体激动剂,已成为心力衰竭动物模型和人类研究的焦点。GLP-1受体激动剂的有限初步数据显示,其在收缩功能、血流动力学和生活质量方面有潜在改善,这构成了当前II期试验的基础。

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