Growing concerns about using hypoxia-inducible factor prolyl hydroxylase inhibitors for the treatment of renal anemia

被引:7
|
作者
Nakanishi, Takeshi [1 ,2 ]
Kuragano, Takahiro [1 ]
机构
[1] Hyogo Med Univ, Dept Internal Med, Div Kidney Dialysis & Cardiol, Nishinomiya, Japan
[2] Gojinkai Sumiyoshigawa Hosp, Dept Nephrol, Kobe, Japan
关键词
2-oxoglutarate-dependent dioxygenases; alpha-ketoglutarate; epigenetics; HIF-PHIs; renal anemia; CHRONIC KIDNEY-DISEASE; FACTOR PATHWAY INHIBITOR; ALPHA-KETOGLUTARATE; ROXADUSTAT FG-4592; TISSUE FACTOR; MYOCARDIAL-INFARCTION; ENERGY-METABOLISM; RESPONSE ELEMENT; HEART; DYSFUNCTION;
D O I
10.1093/ckj/sfae051
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 inhibitors (HIF-PHIs) have emerged as a novel therapeutic class for treating anemia in patients with chronic kidney disease. Small molecule analogs of alpha-ketoglutarate (AKG), an essential substrate for 2-oxoglutarate-dependent dioxygenases (2-OGDDs), including prolyl hydroxylase domain proteins (PHDs), inhibit PHDs pharmacologically and thereby prevent HIF degradation. HIF stabilization alleviates anemia through several stimulatory effects on erythropoiesis, but it also affects the expression of many anemia-unrelated genes whose protein products exert important functions in vivo. Therefore, the pleiotropic effects of HIF stabilization under normoxic conditions deserve to be examined in more detail. Specifically, we believe that particular attention should be given to epigenetic modifications among the various AKG-based metabolic systems that may be altered by HIF-PHIs. It is noteworthy that AKG has been reported to exert health-protective actions. AKG-based metabolic systems include enzymes associated with the tricarboxylic acid cycle and amino acid metabolism, as well as 2-OGDD-mediated processes, which play important roles in many biological reactions. In this review, we examine the multifaceted effects of HIF-PHIs, encompassing not only their on-target effect of HIF stabilization but also their off-target inhibitory effects on various AKG-based metabolic systems. Furthermore, we examine its potential relevance to cardiovascular complications, based on clinical and animal studies suggesting its involvement in vascular calcification, thrombogenesis and heart failure. In conclusion, although HIF-PHIs offer a promising avenue for anemia treatment in CKD patients, their broader impact on multiple biological systems raises substantial concerns. The intricate interplay between HIF stabilization, AKG competition and cardiovascular complications warrants extensive, long-term investigations to ensure the safety and usefulness of HIF-PHIs in clinical practice.
引用
收藏
页数:11
相关论文
共 50 条
  • [32] Activation of the hypoxia-inducible factor pathway and stimulation of angiogenesis by application of prolyl hydroxylase inhibitors
    Warnecke, C
    Griethe, W
    Weidemann, A
    Jürgensen, JS
    Willam, C
    Bachmann, S
    Ivashchenko, Y
    Wagner, I
    Frei, U
    Wiesener, M
    Eckardt, KU
    FASEB JOURNAL, 2003, 17 (06): : 1186 - +
  • [33] Hypoxia-inducible Factor Prolyl Hydroxylase Inhibitors and Hypothyroidism: An Analysis of the Japanese Pharmacovigilance Database
    Tanaka, Hiroyuki
    Tani, Alicia
    Onoda, Toshihisa
    Ishii, Toshihiro
    IN VIVO, 2024, 38 (02): : 917 - 922
  • [34] Discovery of Orally Bioavailable and Liver-Targeted Hypoxia-Inducible Factor Prolyl Hydroxylase (HIF-PHD) Inhibitors for the Treatment of Anemia
    Liu, Ping
    Wang, Liping
    DuBois, Byron G.
    Colandrea, Vincent J.
    Liu, Rongqiang
    Cai, Jiaqiang
    Du, Xiaoxing
    Quan, Weiro
    Morris, William
    Bai, Jianwu
    Bishwokarma, Bimjhana
    Cheng, Mangeng
    Piesvaux, Jennifer
    Ray, Kallol
    Alpert, Carla
    Chiu, Chi-Sung
    Zielstorff, Mark
    Metzger, Joseph M.
    Yang, Liming
    Leung, Dennis
    Alleyne, Candice
    Vincent, Stella H.
    Pucci, Vincenzo
    Li, Xiaofang
    Crespo, Alejandro
    Stickens, Dominique
    Hale, Jeffrey J.
    Ujjainwalla, Feroze
    Sinz, Christopher J.
    ACS MEDICINAL CHEMISTRY LETTERS, 2018, 9 (12): : 1193 - 1198
  • [35] Mucosal protection by hypoxia-inducible factor prolyl hydroxylase inhibition
    Robinson, Andreas
    Keely, Simon
    Karhausen, Joern
    Gerich, Mark E.
    Furuta, Glenn T.
    Colgan, Sean P.
    GASTROENTEROLOGY, 2008, 134 (01) : 145 - 155
  • [36] Daprodustat Hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitor Treatment of anemia associated with chronic kidney disease
    Gras, J.
    DRUGS OF THE FUTURE, 2017, 42 (06) : 327 - 333
  • [37] VADADUSTAT Hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitor Treatment of anemia secondary to chronic kidney disease
    Cole, P.
    DRUGS OF THE FUTURE, 2016, 41 (10) : 601 - 606
  • [38] Daprodustat: A Hypoxia-Inducible Factor-Prolyl Hydroxylase Inhibitor for Anemia of Chronic Kidney Disease
    Johnson, Haley N.
    Prasad-Reddy, Lalita
    ANNALS OF PHARMACOTHERAPY, 2025, 59 (01) : 71 - 80
  • [39] The anaemia treatment journey of CKD patients: from epoetins to hypoxia-inducible factor-prolyl hydroxylase inhibitors
    Locatelli, Francesco
    Del Vecchio, Lucia
    Elliott, Steve
    CLINICAL KIDNEY JOURNAL, 2023, 16 (10) : 1563 - 1579
  • [40] Current treatment practices for anemia in patients with chronic kidney disease and future opportunities with hypoxia-inducible factor prolyl hydroxylase inhibitors: a narrative review
    Kile, Mercedes
    Sudchada, Patcharaporn
    INTERNATIONAL UROLOGY AND NEPHROLOGY, 2021, 53 (02) : 283 - 290