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Review
. 2021 Feb;26(2):105-118.
doi: 10.1111/nep.13835. Epub 2020 Dec 9.

Recommendations by the Asian Pacific society of nephrology (APSN) on the appropriate use of HIF-PH inhibitors

Affiliations
Review

Recommendations by the Asian Pacific society of nephrology (APSN) on the appropriate use of HIF-PH inhibitors

Desmond Y H Yap et al. Nephrology (Carlton). 2021 Feb.

Abstract

Renal anaemia is a common and important complication in patients with chronic kidney disease (CKD). The current standard-of-care treatment for renal anaemia in CKD patients involves ensuring adequate iron stores and administration of erythropoietin stimulating agents (ESA). Hypoxia inducible factor (HIF) is a key transcription factor primarily involved in the cellular regulation and efficiency of oxygen delivery. Manipulation of the HIF pathway by the use of HIF-prolyl hydroxylase inhibitors (HIF-PHI) has emerged as a novel approach for renal anaemia management. Despite it being approved for clinical use in various Asia-Pacific countries, its novelty mandates the need for nephrologists and clinicians generally in the region to well understand potential benefits and harms when prescribing this class of drug. The Asian Pacific society of nephrology HIF-PHI Recommendation Committee, formed by a panel of 11 nephrologists from the Asia-Pacific region who have clinical experience or have been investigators in HIF-PHI studies, reviewed and deliberated on the clinical and preclinical data concerning HIF-PHI. This recommendation summarizes the consensus views of the committee regarding the use of HIF-PHI, taking into account both available data and expert opinion in areas where evidence remains scarce.

Keywords: Asian Pacific; anaemia; chronic kidney disease; hypoxia inducible factor; prolyl hydroxylase inhibitor.

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Conflict of interest statement

Masaomi Nangaku received honorarium, advisory fees and research grants from KyowaKirin, GSK, Astellas, AstraZeneca, Akebia, Mitsubishi‐Tanabe, JT and Bayer. Lawrence McMahon (ANZSN) is National PI in Clinical Trial with Akebia and received advisory fees from Pfizer and AstraZeneca, research funding from Amgen and Roche. Chuan‐ming Hao (CSN) received honorarium from Fibrogen and AstraZeneca. Nan Hu (CSN) received research grant from CAMS Innovation Fund for Medical Sciences (2019‐I2M‐5‐046). Desmond Yap (HKSN) received research grants and advisory fees from GSK and AstraZeneca. Hirokazu Okada (JSN) received honorarium, advisory fees and research grants from Kyowa Kirin, Daiichi Sankyo, Mitsubishi Tanabe, Takeda, Chugai, Torii, Astellas, and MSD. Yusuke Suzuki (JSN) received honorarium, advisory fees and research grants from Kyowa Kirin, Mitsubishi‐Tanabe, Daiichi‐Sankyo, Novartis, Chugai. Sung Gyun Kim (KSN) received honorarium, advisory fees and research grants from Fibrogen, GSK, Akebia, JW Pharmaceutical and KyowaKirin. Soo Kun Lim (MSN) received honorarium, advisory fees and research grants from AstraZeneca, Baxter, Boehringer Ingelheim, Fresenius Kabi, Fresenius Medical Care, Novartis, Novo Nordisk, and Sanofi.

Kriengsak Vareesangthip (NST) received honorarium and advisory fee from AstraZeneca, Fresenius Kabi, Siam Bioscience and Novo Nordisk. Chi‐Chih Hung (TSN) has no conflicts of interest to disclose.

References

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