Chronic kidney disease-associated anemia: new remedies.

Lucia Del Vecchio, Andrea Cavalli, Benedetta Tucci, Francesco Locatelli
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Abstract

Erythropoiesis stimulating agents (ESAs) are effective drugs that correct anemia in patients with chronic kidney disease (CKD). Recombinant human erythropoietin (EPO), the first ESA that became available more than 20 years ago, is similar to the naturally occurring molecule. In subsequent years, pharmacological research focused on the development of new agents with improved characteristics, with the creation of high molecular weight ESAs having been the first approach. In more recent years, new agents have been developed, including peginesatide (Hematide; Affymax Inc/Takeda Pharmaceutical Co Ltd), which is a dimeric peptide with a chemical structure unrelated to EPO that is being evaluated in phase III clinical trials. In addition, the clinical development of two inhibitors of hypoxia-inducible transcription factor has been resumed recently, while other approaches, such as gene therapy and EPO fusion proteins, and the inhibition of GATA and hematopoietic cell phosphatase remain far from being applicable in clinical practice. New iron compounds, which are becoming increasingly available, will facilitate an integrated approach to anemia management using both iron and/or ESAs, according to the clinical needs of patients. This review discusses new therapeutic options (already available or still under development) for the treatment of CKD-associated anemia, including ESAs and intravenous iron molecules.

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慢性肾病相关性贫血:新的治疗方法。
促红细胞生成剂(ESAs)是治疗慢性肾脏疾病(CKD)患者贫血的有效药物。重组人促红细胞生成素(EPO)是20多年前第一个可用的ESA,与自然产生的分子相似。在随后的几年里,药理学研究的重点是开发具有改进特性的新药物,高分子量esa的创建是第一个方法。近年来,开发了新的药物,包括peginesatide (Hematide;Affymax Inc/Takeda Pharmaceutical Co Ltd)是一种二聚体肽,其化学结构与EPO无关,正在进行III期临床试验评估。此外,最近两种缺氧诱导转录因子抑制剂的临床开发已经恢复,而其他方法,如基因治疗和EPO融合蛋白,以及GATA和造血细胞磷酸酶的抑制还远远不能应用于临床实践。越来越多的新铁化合物将根据患者的临床需要,促进使用铁和/或esa的贫血管理综合方法。这篇综述讨论了治疗ckd相关性贫血的新治疗选择(已经可用或仍在开发中),包括esa和静脉注射铁分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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