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New options for the anemia of chronic kidney disease

机译:慢性肾病贫血的新选择

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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:贫血是慢性肾病的常见并发症。自1990年以来,使用促红细胞生成刺激剂(ESA)一直是治疗的主干。一系列大型试验表明ESA具有严重的安全问题,包括增加心血管和血栓形成事件和死亡。分析表明高药理学剂量的ESA,而不是高度取得的血红蛋白,可能会介导伤害。缺氧诱导因子(HIF)活化剂刺激内源性促红细胞生成素的生产,增强铁可用性。在早期的临床试验中,这些口腔器似乎能够取代ESA治疗并最大限度地减少对I.V的需求。慢性肾病相关贫血的铁疗法,同时具有其他潜在的有利行为。几种HIF激活剂正在进行大期3阶段试验。该评论评论评论贫血管理趋势,与我们目前的疗法有关的安全问题,HIF在调节红细胞的作用以及HIF激活剂的不同行动。

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