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New options for the anemia of chronic kidney disease:Changing the Paradigms for the Treatment of Chronic Kidney Disease

机译:慢性肾脏病贫血的新选择:改变治疗慢性肾脏病的范例

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摘要

Anemia is a common complication of chronic kidney disease. Use of erythropoiesis-stimulating agents (ESA) has been a mainstay of treatment since 1990. A series of large trials demonstrated that ESAs have serious safety problems, including increasing cardiovascular and thrombotic events, and death. Analyses suggest high pharmacologic doses of ESAs, rather than the highly achieved hemoglobin, may mediate harm. Hypoxia-inducible factor (HIF) activators stimulate endogenous erythropoietin production and enhance iron availability. In early clinical trials, these oral agents appear to be capable of replacing ESA therapy and minimizing the need for i.v. iron therapy for chronic kidney disease–related anemia, while having other potentially advantageous actions. Large phase 3 trials are underway with several HIF activators. This commentary reviews trends in anemia management, the safety issues related to our present therapies, the role of HIF in regulating erythropoiesis, and the diverse actions of HIF activators.
机译:贫血是慢性肾脏疾病的常见并发症。自1990年以来,使用促红细胞生成素(ESA)一直是治疗的主要手段。一系列大型试验表明,ESA存在严重的安全问题,包括心血管和血栓形成事件增加以及死亡。分析表明高药理剂量的ESA可能会介导伤害,而不是高度获得的血红蛋白。缺氧诱导因子(HIF)激活剂刺激内源性促红细胞生成素的产生并提高铁的利用率。在早期的临床试验中,这些口服药物似乎能够替代ESA治疗,并最大程度地减少了静脉注射的需要。铁疗法可治疗慢性肾脏病相关的贫血,同时具有其他潜在的有益作用。目前正在使用几种HIF激活剂进行大型3期试验。本文评论了贫血管理的趋势,与我们目前疗法有关的安全性问题,HIF在调节红细胞生成中的作用以及HIF激活剂的多种作用。

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