Wish Jay B
Division of Nephrology, IU Health University Hospital, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Kidney Int Rep. 2021 Jun 9;6(10):2540-2553. doi: 10.1016/j.ekir.2021.05.028. eCollection 2021 Oct.
Anemia is common in patients with chronic kidney disease. Treatment with erythropoiesis-stimulating agents has decreased transfusion rates, but has not been consistently shown to improve cardiovascular outcomes or quality of life. Moreover, treatment to hemoglobin levels normal for the general population (13-14 g/dL) has resulted in increased cardiovascular morbidity and mortality versus lower hemoglobin targets, and some patients with chronic kidney disease do not reach these lower hemoglobin targets despite escalating doses of erythropoiesis-stimulating agents. The pathophysiology of anemia in patients with chronic kidney disease has been informed by the discovery of hypoxia-inducible factor and hepcidin pathways. Recent innovations in anemia treatment leverage knowledge of these pathways to effectively raise hemoglobin levels independent of erythropoiesis-stimulating agent administration. Several agents that stabilize hypoxia-inducible factor are undergoing or have completed phase 3 clinical trials. These agents appear to have equal efficacy as erythropoiesis-stimulating agents in raising hemoglobin levels and have not been associated with major safety signals to date. Because of the potential for off-target effects from non-anemia-related gene transcription by hypoxia-inducible factor stabilization, longer-term follow-up studies and registries will be needed to ensure safety. Agents that modulate hepcidin have undergone early clinical trials with mixed results regarding safety and efficacy in increasing hemoglobin levels. Sodium-glucose cotransporter 2 inhibitors, which also decrease hepcidin levels, have been associated with increased hemoglobin levels among patients with chronic kidney disease in clinical trials exploring proteinuria and kidney disease progression.
贫血在慢性肾脏病患者中很常见。使用促红细胞生成素治疗可降低输血率,但一直未显示能改善心血管结局或生活质量。此外,将血红蛋白水平提升至一般人群正常水平(13 - 14 g/dL)与较低血红蛋白目标相比,已导致心血管发病率和死亡率增加,并且一些慢性肾脏病患者尽管促红细胞生成素剂量不断增加,仍未达到这些较低的血红蛋白目标。慢性肾脏病患者贫血的病理生理学已因缺氧诱导因子和铁调素途径的发现而得到阐释。贫血治疗的最新创新利用了这些途径的知识,以在不依赖促红细胞生成素给药的情况下有效提高血红蛋白水平。几种稳定缺氧诱导因子的药物正在进行或已完成3期临床试验。这些药物在提高血红蛋白水平方面似乎与促红细胞生成素具有同等疗效,并且迄今为止尚未发现重大安全信号。由于缺氧诱导因子稳定可能导致与非贫血相关基因转录的脱靶效应,因此需要进行长期随访研究和登记以确保安全性。调节铁调素的药物已进行了早期临床试验,在提高血红蛋白水平方面的安全性和疗效结果不一。钠 - 葡萄糖协同转运蛋白2抑制剂也可降低铁调素水平,在探索蛋白尿和肾脏疾病进展的临床试验中,已发现其与慢性肾脏病患者血红蛋白水平升高有关。