4.7 Article

Hypoxia-inducible factor-prolyl hydroxylase inhibitors for renal anemia in chronic kidney disease: Advantages and disadvantages

期刊

EUROPEAN JOURNAL OF PHARMACOLOGY
卷 912, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.ejphar.2021.174583

关键词

Chronic kidney disease (CKD); End-stage renal disease; Erythropoiesis-stimulating agents (ESAs); Hypoxia-inducible factor-prolyl hydroxylase domain inhibitors (HIF-PHIs); Vascular endothelial growth factor (VEGF)

资金

  1. Osaka Kidney Foundation [OKF21-0003]

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Anemia is a common feature and complication of chronic kidney disease (CKD), with treatments such as ESAs and HIF-PHIs being widely used. HIF-PHIs show promise in improving renal anemia treatment by lowering hepcidin levels, modulating iron metabolism, reducing inflammation, and oxidative stress. However, further studies are needed to evaluate the long-term effects and potential risks of HIF-PHIs in clinical practice.
Anemia is a common feature and complication of chronic kidney disease (CKD). Erythropoiesis-stimulating agents (ESAs) and recombinant human erythropoietin have been used widely in renal anemia treatment. Recently, hypoxia-inducible factor-prolyl hydroxylase domain inhibitors (HIF-PHIs) that may improve the treatment of renal anemia patients were launched. Previous studies indicated that HIF-PHIs may decrease hepcidin levels and modulate iron metabolism, thereby increasing total iron-binding capacity and reducing the need for iron supplementation. Furthermore, HIF-PHIs can reduce inflammation and oxidative stress in CKD. Recombinant erythropoietin has become a routine treatment for patients with CKD and end-stage renal disease with relatively few adverse effects. However, higher doses of recombinant erythropoietin have been demonstrated to be an independent predictor of mortality in patients under hemodialysis. Phase III clinical trials of HIF-PHIs in patients with anemia and dialysis-dependent CKD have shown their efficacy and safety in both nondialysis and dialysis CKD patients. However, HIF alpha binds to specific hypoxia-response elements in the vascular endothelial growth factor or retinoic acid-related orphan receptor gamma t (ROR gamma t) promoter, which may be involved in the progression of cancer, psoriasis, and rheumatoid arthritis. In this paper, we have summarized the mechanism, clinical application, and clinical trials of HIF-PHIs in the treatment of renal anemia and aimed to provide an overview of the new drugs in clinical practice, as well as reconsider the advantages and disadvantages of HIF-PHIs and ESAs. Presently, there are not enough clinical studies examining the effects of long-term administration of HIF-PHIs. Therefore, further studies will be needed.

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