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

IF 0.7 Q4 UROLOGY & NEPHROLOGY
Case Reports in Nephrology and Dialysis Pub Date : 2022-08-19 eCollection Date: 2022-05-01 DOI:10.1159/000525735
Hironori Nakamura, Shigekazu Kurihara, Mariko Anayama, Yasushi Makino, Masaki Nagasawa
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引用次数: 4

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 divalent metal transporter 1, duodenal cytochrome B, 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.

Abstract Image

4例接受缺氧诱导因子-丙氨酸羟化酶抑制剂治疗的肾性贫血患者血清铜过量:可能的安全问题
铜是人体不可缺少的微量金属元素,主要通过胃和小肠吸收,排泄到胆汁中。缺氧诱导因子-脯氨酸羟化酶抑制剂(HIF-PHIs)已成为肾性贫血管理的新方法。许多与铁吸收有关的肠道基因,包括二价金属转运蛋白1、十二指肠细胞色素B和铜转运蛋白ATPase7A,在缺铁时被HlF-α反激活。我们首次报道了4例肾性贫血患者在服用罗沙司他或达普达司他治疗期间血清铜水平超标,停用HIF-PHI并改用达贝泊汀后血清铜水平降至正常水平,提示HIF-PHI与血清铜过量有关。HIF-PHI调节铁代谢,如铁的吸收、固存和动员,并可能通过增加铜在组织中的吸收和/或再分配而增加血清铜水平。因此,迫切需要研究HIF-PHI使用与血清铜水平之间的相关性,因为铜过量可能涉及几种急性或慢性不良事件。
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
36
审稿时长
10 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.
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