Hypoxia-inducible factor?prolyl hydroxylase inhibitors in the treatment of anemia of chronic kidney disease

被引:111
作者
Haase, Volker H. [1 ,2 ,3 ,4 ]
机构
[1] Vanderbilt Univ, Dept Med, Med Ctr, Nashville, TN 37232 USA
[2] Uppsala Univ, Dept Med Cell Biol, Uppsala, Sweden
[3] Vanderbilt Univ, Sch Med, Dept Mol Physiol, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Sch Med, Program Canc Biol, Nashville, TN 37232 USA
关键词
anemia; chronic kidney disease; erythropoietin; hepcidin; hypoxia-inducible factor; iron; prolyl hydroxylase domain dioxygenase; FACTOR-PROLYL HYDROXYLASE; REGULATORY PEPTIDE HEPCIDIN; ENDOTHELIAL GROWTH-FACTOR; NON-DIALYSIS PATIENTS; QUALITY-OF-LIFE; ROXADUSTAT FG-4592; HUMAN-ERYTHROPOIETIN; RENAL ANEMIA; FACTOR-I; OPEN-LABEL;
D O I
10.1016/j.kisu.2020.12.002
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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. Copyright (C) 2021, International Society of Nephrology. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:8 / 25
页数:18
相关论文
共 161 条
[91]   Hepatic HIF-2 regulates erythropoietic responses to hypoxia in renal anemia [J].
Kapitsinou, Pinelopi P. ;
Liu, Qingdu ;
Unger, Travis L. ;
Rha, Jennifer ;
Davidoff, Olena ;
Keith, Brian ;
Epstein, Jonathan A. ;
Moores, Sheri L. ;
Erickson-Miller, Connie L. ;
Haase, Volker H. .
BLOOD, 2010, 116 (16) :3039-3048
[92]   Identification of erythroferrone as an erythroid regulator of iron metabolism [J].
Kautz, Leon ;
Jung, Grace ;
Valore, Erika V. ;
Rivella, Stefano ;
Nemeth, Elizabeta ;
Ganz, Tomas .
NATURE GENETICS, 2014, 46 (07) :678-684
[93]   Anaemia in kidney disease: harnessing hypoxia responses for therapy [J].
Koury, Mark J. ;
Haase, Volker H. .
NATURE REVIEWS NEPHROLOGY, 2015, 11 (07) :394-410
[94]   HIF-1α promotes cyst progression in a mouse model of autosomal dominant polycystic kidney disease [J].
Kraus, Andre ;
Peters, Dorien J. M. ;
Klanke, Bernd ;
Weidemann, Alexander ;
Willam, Carsten ;
Schley, Gunnar ;
Kunzelmann, Karl ;
Eckardt, Kai-Uwe ;
Buchholz, Bjoern .
KIDNEY INTERNATIONAL, 2018, 94 (05) :887-899
[95]   FIH-1 is an asparaginyl hydroxylase enzyme that regulates the transcriptional activity of hypoxia-inducible factor [J].
Lando, D ;
Peet, DJ ;
Gorman, JJ ;
Whelan, DA ;
Whitelaw, ML ;
Bruick, RK .
GENES & DEVELOPMENT, 2002, 16 (12) :1466-1471
[96]   TRANSCRIPTIONAL REGULATION OF THE RAT VASCULAR ENDOTHELIAL GROWTH-FACTOR GENE BY HYPOXIA [J].
LEVY, AP ;
LEVY, NS ;
WEGNER, S ;
GOLDBERG, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (22) :13333-13340
[97]   CLONING AND EXPRESSION OF THE HUMAN ERYTHROPOIETIN GENE [J].
LIN, FK ;
SUGGS, S ;
LIN, CH ;
BROWNE, JK ;
SMALLING, R ;
EGRIE, JC ;
CHEN, KK ;
FOX, GM ;
MARTIN, F ;
STABINSKY, Z ;
BADRAWI, SM ;
LAI, PH ;
GOLDWASSER, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (22) :7580-7584
[98]   Ischaemia-induced retinal neovascularisation and diabetic retinopathy in mice with conditional knockout of hypoxia-inducible factor-1 in retinal Muller cells [J].
Lin, M. ;
Chen, Y. ;
Jin, J. ;
Hu, Y. ;
Zhou, K. K. ;
Zhu, M. ;
Le, Y. -Z. ;
Ge, J. ;
Johnson, R. S. ;
Ma, J. -X. .
DIABETOLOGIA, 2011, 54 (06) :1554-1566
[99]   Hypoxia, HIF, and Associated Signaling Networks in Chronic Kidney Disease [J].
Liu, Jing ;
Wei, Qingqing ;
Guo, Chunyuan ;
Dong, Guie ;
Liu, Yu ;
Tang, Chengyuan ;
Dong, Zheng .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (05)
[100]   Hypoxia-inducible factor regulates hepcidin via erythropoietin-induced erythropoiesis [J].
Liu, Qingdu ;
Davidoff, Olena ;
Niss, Knut ;
Haase, Volker H. .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (12) :4635-4644