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A retrospective study on the efficacy of Roxadustat in peritoneal dialysis patients with erythropoietin hyporesponsiveness

  • Jie Liu (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Shuang Li (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Fan Yang (Department of Nephrology, Beijing Aerospace General Hospital) ;
  • Tianyu Li (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Rui Li (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Yousuf Waheed (Department of Nephrology, Affiliated Hospital of Xuzhou Medical University) ;
  • Chen Meng (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Shulin Li (Department of Nephrology, Affiliated Hospital of Xuzhou Medical University) ;
  • Kun Liu (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Yanshan Tong (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Haisheng Xu (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Chuankuo Tian (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University) ;
  • Xinglei Zhou (Department of Nephrology, The Second Affiliated Hospital of Xuzhou Medical University)
  • Received : 2023.11.27
  • Accepted : 2024.02.20
  • Published : 2024.05.01

Abstract

Background/Aims: Roxadustat, an oral medication for treating renal anemia, is a hypoxia-inducible factor prolyl hydroxylase inhibitor used for regulating iron metabolism and promoting erythropoiesis. To investigate the efficacy and safety of roxadustat in patients undergoing peritoneal dialysis (PD) with erythropoietin hyporesponsiveness. Methods: Single-center, retrospective study, 81 PD patients (with erythropoietin hyporesponsiveness) were divided into the roxadustat group (n = 61) and erythropoiesis-stimulating agents (ESAs) group (n = 20). Hemoglobin (Hb), total cholesterol, intact parathyroid hormone (iPTH), brain natriuretic peptide (BNP), related indicators of cardiac function and high-sensitivity C-reactive protein (hs-CRP) were collected. Additionally, adverse events were also recorded. The follow-up period was 16 weeks. Results: The two groups exhibited similar baseline demographic and clinical characteristics. At baseline, the roxadustat group had a mean Hb level of 89.8 ± 18.9 g/L, while the ESAs group had a mean Hb level of 95.2 ± 16.0 g/L. By week 16, the Hb levels had increased to 118 ± 19.8 g/L (p < 0.05) in the roxadustat group and 101 ± 19.3 g/L (p > 0.05) in the ESAs group. The efficacy of roxadustat in improving anemia was not influenced by baseline levels of hs-CRP and iPTH. Cholesterol was decreased in the roxadustat group without statin use. An increase in left ventricular ejection fraction and stabilization of BNP were observed in the roxadustat group. Conclusions: For PD patients with erythropoietin hyporesponsiveness, roxadustat can significantly improve renal anemia. The efficacy of roxadustat in improving renal anemia was not affected by baseline levels of hs-CRP0 and iPTH.

Keywords

Acknowledgement

We would like to express our sincere thanks to every member of our research team for their hard-work and the strong support provided by the hospital.

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