Erythropoietin in Myocardial Infarction: Experimental Evidence and Clinical Studies

I. Ott, D. Herzzentrum, A. Stein, Deutsches Herzzentrum der Technischen
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引用次数: 2

Abstract

Erythropoietin produced mainly in the kidney is the main regulator of erythropoiesis. Experimental studies identified additional, non-haematopoietic, protective effects during myocardial ischemia and reperfusion due to inhibition of apoptosis, stimulation of vasculogenesis and progenitor cell mobilisation. Based on these findings, five prospective, randomised, clinical trials have been performed. A short term regimen of erythropoietin was applied during PCI in patients with STEMI up to a cumulative dose of 100.000 IU. No changes in myocardial function or infarct size were observed after erythropoietin. Yet in two studies an increase in adverse events after erythropoietin was observed, whereas one study found an increase in major adverse clinical events in the control group. This review discusses experimental evidence of erythropoietin in acute myocardial infarction and its failure in clinical trials.
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促红细胞生成素在心肌梗死中的作用:实验证据和临床研究
促红细胞生成素主要产生于肾脏,是促红细胞生成的主要调节因子。实验研究发现,在心肌缺血和再灌注过程中,由于抑制细胞凋亡、刺激血管生成和祖细胞动员,还具有额外的、非造血的保护作用。基于这些发现,进行了五项前瞻性随机临床试验。STEMI患者在PCI治疗期间给予促红细胞生成素短期治疗方案,累计剂量为100,000 IU。促红细胞生成素治疗后心肌功能和梗死面积未见明显变化。然而,在两项研究中观察到促红细胞生成素后不良事件的增加,而一项研究发现对照组的主要临床不良事件增加。本文综述了促红细胞生成素治疗急性心肌梗死的实验证据及其在临床试验中的失败。
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