| Literature DB >> 33777492 |
Volker H Haase1,2,3.
Abstract
Hypoxia-inducible factor-prolyl hydroxylase domain inhibitors (HIF-PHIs) are a promising new class of orally administered drugs currently in late-stage global clinical development for the treatment of anemia of chronic kidney disease (CKD). HIF-PHIs activate the HIF oxygen-sensing pathway and are efficacious in correcting and maintaining hemoglobin levels in patients with non-dialysis- and dialysis-dependent CKD. In addition to promoting erythropoiesis through the increase in endogenous erythropoietin production, HIF-PHIs reduce hepcidin levels and modulate iron metabolism, providing increases in total iron binding capacity and transferrin levels, and potentially reducing the need for i.v. iron supplementation. Furthermore, HIF-activating drugs are predicted to have effects that extend beyond erythropoiesis. This review summarizes clinical data from current HIF-PHI trials in patients with anemia of CKD, discusses mechanisms of action and pharmacologic properties of HIF-PHIs, and deliberates over safety concerns and potential impact on anemia management in patients with CKD.Entities:
Keywords: anemia; chronic kidney disease; erythropoietin; hepcidin; hypoxia-inducible factor; iron; prolyl hydroxylase domain dioxygenase
Year: 2021 PMID: 33777492 PMCID: PMC7983025 DOI: 10.1016/j.kisu.2020.12.002
Source DB: PubMed Journal: Kidney Int Suppl (2011) ISSN: 2157-1716