AI Article Synopsis

  • The National Kidney Foundation held a workshop in March 2019 to explore a new treatment option—hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHIs)—for anemia in chronic kidney disease (CKD) patients.
  • Experts from various fields discussed current anemia treatments, the biology behind HIF, the pharmacology of HIF-PHIs, and reviewed phase 2 clinical trial results for these drugs in both dialysis and non-dialysis patients.
  • Recommendations from the workshop highlighted the need for further investigation into HIF-PHIs regarding their long-term safety, potential benefits, and the importance of educating patients and providers for implementation.

Article Abstract

The National Kidney Foundation convened an interdisciplinary international workshop in March 2019 to discuss the potential role of a new class of agents for the treatment of anemia in patients with chronic kidney disease (CKD): the hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHIs). International experts with expertise in physiology, biochemistry, structural chemistry, translational medicine, and clinical management of anemia participated. Participants reviewed the unmet needs of current anemia treatment, the biology of hypoxia-inducible factor, the pharmacology of prolyl hydroxylase inhibitors, and the results of phase 2 clinical trials of HIF-PHIs among patients with CKD, both those treated by dialysis and those not receiving kidney replacement therapy. The results of key phase 3 clinical trials of HIF-PHIs available as of the time of writing are also included in this report, although they appeared after the workshop was completed. Participants in the workshop developed a number of recommendations for further examination of HIF-PHIs, which are summarized in this report and include long-term safety issues, potential benefits, and practical considerations for implementation including patient and provider education.

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Source
http://dx.doi.org/10.1053/j.ajkd.2021.06.019DOI Listing

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