Current Status of Renal Anemia Pharmacotherapy—What Can We Offer Today
Chronic kidney disease (CKD) is one of the fastest-growing major causes of death internationally. Better treatment of CKD and its complications is crucial to reverse this negative trend. Anemia is a frequent complication of CKD and is associated with unfavorable clinical outcomes. It is a devastatin...
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doaj-8219200934e44d9096f5d311b7a625b62021-09-26T00:28:19ZengMDPI AGJournal of Clinical Medicine2077-03832021-09-01104149414910.3390/jcm10184149Current Status of Renal Anemia Pharmacotherapy—What Can We Offer TodayBartłomiej Borawski0Jacek Stanislaw Malyszko1Marlena Kwiatkowska2Jolanta Malyszko3Department of Nephrology, Dialysis and Internal Medicine, Medical University of Warsaw, Banacha 1A, 02-097 Warsaw, Poland1st Department of Nephrology and Transplantology, Medical University of Bialystok, 15-540 Bialystok, PolandDepartment of Nephrology, Dialysis and Internal Medicine, Medical University of Warsaw, Banacha 1A, 02-097 Warsaw, PolandDepartment of Nephrology, Dialysis and Internal Medicine, Medical University of Warsaw, Banacha 1A, 02-097 Warsaw, PolandChronic kidney disease (CKD) is one of the fastest-growing major causes of death internationally. Better treatment of CKD and its complications is crucial to reverse this negative trend. Anemia is a frequent complication of CKD and is associated with unfavorable clinical outcomes. It is a devastating complication of progressive kidney disease, that negatively affects also the quality of life. The prevalence of anemia increases in parallel with CKD progression. The aim of this review is to summarize the current knowledge on therapy of renal anemia. Iron therapy, blood transfusions, and erythropoietin stimulating agents are still the mainstay of renal anemia treatment. There are several novel agents on the horizon that might provide therapeutic opportunities in CKD. The potential therapeutic options target the hepcidin–ferroportin axis, which is the master regulator of iron homeostasis, and the BMP-SMAD pathway, which regulates hepcidin expression in the liver. An inhibition of prolyl hydroxylase is a new therapeutic option becoming available for the treatment of anemia in CKD patients. This new class of drugs stimulates the synthesis of endogenous erythropoietin and increases iron availability. We also summarized the effects of prolyl hydroxylase inhibitors on iron parameters, including hepcidin, as their action on the hematological parameters. They could be of particular interest in the out-patient population with CKD and patients with ESA hyporesponsiveness. However, current knowledge is limited and still awaits clinical validation. One should be aware of the potential risks and benefits of novel, sophisticated therapies.https://www.mdpi.com/2077-0383/10/18/4149anemiachronic kidney diseasehemodialysisESAironhepcidin |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Bartłomiej Borawski Jacek Stanislaw Malyszko Marlena Kwiatkowska Jolanta Malyszko |
spellingShingle |
Bartłomiej Borawski Jacek Stanislaw Malyszko Marlena Kwiatkowska Jolanta Malyszko Current Status of Renal Anemia Pharmacotherapy—What Can We Offer Today Journal of Clinical Medicine anemia chronic kidney disease hemodialysis ESA iron hepcidin |
author_facet |
Bartłomiej Borawski Jacek Stanislaw Malyszko Marlena Kwiatkowska Jolanta Malyszko |
author_sort |
Bartłomiej Borawski |
title |
Current Status of Renal Anemia Pharmacotherapy—What Can We Offer Today |
title_short |
Current Status of Renal Anemia Pharmacotherapy—What Can We Offer Today |
title_full |
Current Status of Renal Anemia Pharmacotherapy—What Can We Offer Today |
title_fullStr |
Current Status of Renal Anemia Pharmacotherapy—What Can We Offer Today |
title_full_unstemmed |
Current Status of Renal Anemia Pharmacotherapy—What Can We Offer Today |
title_sort |
current status of renal anemia pharmacotherapy—what can we offer today |
publisher |
MDPI AG |
series |
Journal of Clinical Medicine |
issn |
2077-0383 |
publishDate |
2021-09-01 |
description |
Chronic kidney disease (CKD) is one of the fastest-growing major causes of death internationally. Better treatment of CKD and its complications is crucial to reverse this negative trend. Anemia is a frequent complication of CKD and is associated with unfavorable clinical outcomes. It is a devastating complication of progressive kidney disease, that negatively affects also the quality of life. The prevalence of anemia increases in parallel with CKD progression. The aim of this review is to summarize the current knowledge on therapy of renal anemia. Iron therapy, blood transfusions, and erythropoietin stimulating agents are still the mainstay of renal anemia treatment. There are several novel agents on the horizon that might provide therapeutic opportunities in CKD. The potential therapeutic options target the hepcidin–ferroportin axis, which is the master regulator of iron homeostasis, and the BMP-SMAD pathway, which regulates hepcidin expression in the liver. An inhibition of prolyl hydroxylase is a new therapeutic option becoming available for the treatment of anemia in CKD patients. This new class of drugs stimulates the synthesis of endogenous erythropoietin and increases iron availability. We also summarized the effects of prolyl hydroxylase inhibitors on iron parameters, including hepcidin, as their action on the hematological parameters. They could be of particular interest in the out-patient population with CKD and patients with ESA hyporesponsiveness. However, current knowledge is limited and still awaits clinical validation. One should be aware of the potential risks and benefits of novel, sophisticated therapies. |
topic |
anemia chronic kidney disease hemodialysis ESA iron hepcidin |
url |
https://www.mdpi.com/2077-0383/10/18/4149 |
work_keys_str_mv |
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