Department of Nephrology, Multidisciplinary Innovation Center for Nephrology, The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Nephrology Research Institute, Shandong University, Jinan, China.
Front Endocrinol (Lausanne). 2024 Jul 1;15:1372150. doi: 10.3389/fendo.2024.1372150. eCollection 2024.
Erythropoietin resistance is present in some patients with chronic kidney disease, especially in those undergoing hemodialysis, and is often treated using roxadustat rather than iron supplements and erythropoiesis-stimulating agents (ESAs). However, some patients cannot afford full doses of roxadustat. This retrospective study investigated the efficacy of low-dose roxadustat combined with recombinant human erythropoietin (rhuEPO) therapy in 39 patients with erythropoietin-resistant renal anemia undergoing maintenance hemodialysis (3-4 sessions/week).
The ability of the combination of low-dose roxadustat and rhuEPO to increase the hemoglobin concentration over 12 weeks was assessed. Markers of iron metabolism were evaluated. Eligible adults received 50-60% of the recommended dose of roxadustat and higher doses of rhuEPO.
The mean hemoglobin level increased from 77.67 ± 11.18 g/dL to 92.0 ± 8.35 g/dL after treatment, and the hemoglobin response rate increased to 72%. The mean hematocrit level significantly increased from 24.26 ± 3.99% to 30.04 ± 3.69%. The soluble transferrin receptor level increased (27.29 ± 13.60 mg/L to 38.09 ± 12.78 mg/L), while the total iron binding capacity (49.22 ± 11.29 mg/L to 43.91 ± 12.88 mg/L) and ferritin level (171.05 ± 54.75 ng/mL to 140.83 ± 42.03 ng/mL) decreased.
Therefore, in patients with ESA-resistant anemia who are undergoing hemodialysis, the combination of low-dose roxadustat and rhuEPO effectively improves renal anemia and iron metabolism.
红细胞生成素抵抗存在于一些慢性肾脏病患者中,尤其是接受血液透析的患者,通常使用罗沙司他而不是铁补充剂和红细胞生成素刺激剂(ESAs)进行治疗。然而,一些患者无法负担罗沙司他的全剂量。本回顾性研究调查了低剂量罗沙司他联合重组人红细胞生成素(rhuEPO)治疗 39 例接受维持性血液透析(每周 3-4 次)的红细胞生成素抵抗性肾性贫血患者的疗效。
评估低剂量罗沙司他和 rhuEPO 联合治疗在 12 周内增加血红蛋白浓度的能力。评估铁代谢标志物。符合条件的成年人接受 50-60%的罗沙司他推荐剂量和更高剂量的 rhuEPO。
治疗后血红蛋白水平从 77.67±11.18g/dL 平均增加到 92.0±8.35g/dL,血红蛋白反应率增加到 72%。平均血细胞比容水平从 24.26±3.99%显著增加到 30.04±3.69%。可溶性转铁蛋白受体水平升高(27.29±13.60mg/L 至 38.09±12.78mg/L),而总铁结合能力(49.22±11.29mg/L 至 43.91±12.88mg/L)和铁蛋白水平(171.05±54.75ng/mL 至 140.83±42.03ng/mL)降低。
因此,在接受血液透析的 ESA 抵抗性贫血患者中,低剂量罗沙司他和 rhuEPO 的联合使用可有效改善肾性贫血和铁代谢。