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4例接受低氧诱导因子脯氨酰羟化酶抑制剂治疗的肾性贫血患者出现血清铜过量:一个可能的安全问题。

Four Cases of Serum Copper Excess in Patients with Renal Anemia Receiving a Hypoxia-Inducible Factor-Prolyl Hydroxylase Inhibitor: A Possible Safety Concern.

作者信息

Nakamura Hironori, Kurihara Shigekazu, Anayama Mariko, Makino Yasushi, Nagasawa Masaki

机构信息

Department of Nephrology, Shinonoi General Hospital, Nagano, Japan.

出版信息

Case Rep Nephrol Dial. 2022 Aug 19;12(2):124-131. doi: 10.1159/000525735. eCollection 2022 May-Aug.

Abstract

Copper is an indispensable trace metal element and is mainly absorbed in the stomach and small intestine and excreted into the bile. Hypoxia-inducible factor-prolyl hydroxylase inhibitors (HIF-PHIs) have emerged as a novel approach for renal anemia management. Many intestinal genes, including , and copper transporter ATPase7A, related to iron absorption are transactivated by HlF-α, during iron deficiency. We first report 4 cases of patients with renal anemia who showed excess in serum copper level during roxadustat or daprodustat treatment, which were decreased to the normal level after discontinuing HIF-PHIs and changing the drug to darbepoetin alfa, suggesting that HIF-PHI is associated with serum copper excess. HIF-PHI modulates iron metabolism, such as iron absorption, sequestration, and mobilization, and may increase serum copper levels by increasing copper absorption and/or redistribution of copper in tissues. Therefore, it is urgent to examine the correlation between HIF-PHI use and serum copper levels because copper excess might be involved in several acute or chronic adverse events.

摘要

铜是一种不可或缺的微量金属元素,主要在胃和小肠中被吸收,并通过胆汁排出。缺氧诱导因子脯氨酰羟化酶抑制剂(HIF-PHIs)已成为治疗肾性贫血的一种新方法。在缺铁期间,许多与铁吸收相关的肠道基因,包括铜转运ATP酶7A,会被HIF-α反式激活。我们首次报告了4例肾性贫血患者,他们在使用罗沙司他或达泊司他治疗期间血清铜水平升高,在停用HIF-PHIs并换用阿法依泊汀后降至正常水平,这表明HIF-PHI与血清铜过量有关。HIF-PHI调节铁代谢,如铁的吸收、螯合和动员,并可能通过增加铜的吸收和/或铜在组织中的重新分布来提高血清铜水平。因此,鉴于铜过量可能与多种急性或慢性不良事件有关,迫切需要研究使用HIF-PHI与血清铜水平之间的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/353d/9459559/02b9465b305f/cnd-0012-0124-g01.jpg

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