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载脂蛋白 E 基因型与辛伐他汀降脂疗效及不良反应相关性的研究进展

Statin-induced rhabdomyolysis from azithromycin interaction in a patient with heterozygous SLCO1B1 polymorphism.

机构信息

Department of Pharmacy Practice, Lipscomb University College of Pharmacy, Nashville, TN, USA.

Department of Pharmacy, Deaconess Health System, Evansville, IN, USA.

出版信息

J Clin Pharm Ther. 2021 Jun;46(3):853-855. doi: 10.1111/jcpt.13327. Epub 2020 Dec 5.

Abstract

WHAT IS KNOWN AND OBJECTIVE

Unlike other macrolide antibiotics, azithromycin is considered safe to co-prescribe with simvastatin. We aim to elucidate the mechanism of a rare azithromycin-simvastatin interaction.

CASE DESCRIPTION

We report a case of simvastatin-induced rhabdomyolysis caused by an azithromycin drug interaction in a patient with heterozygous SLCO1B1 loss-of-function polymorphism. We propose a dual-hit mechanism for this drug-drug-genome interaction. Azithromycin mildly inhibits simvastatin's CYP 3A4 hepatic metabolism, and the SLCO1B1 polymorphism reduces simvastatin hepatic uptake. The combination increases simvastatin serum concentrations significantly, inducing rhabdomyolysis.

WHAT IS NEW AND CONCLUSION

Patients with statin-induced myopathy associated with non-classic CYP inhibitors should be considered for genetic testing and alternative statins with less risk of future interactions.

摘要

已知和目的

与其他大环内酯类抗生素不同,阿奇霉素被认为与辛伐他汀同时使用是安全的。我们旨在阐明阿奇霉素-辛伐他汀相互作用的罕见机制。

病例描述

我们报告了一例杂合子 SLCO1B1 功能丧失性多态性患者中,由于阿奇霉素药物相互作用导致辛伐他汀引起的横纹肌溶解症。我们提出了这种药物-药物-基因组相互作用的双重打击机制。阿奇霉素轻度抑制辛伐他汀的 CYP3A4 肝代谢,而 SLCO1B1 多态性降低了辛伐他汀的肝摄取。这种组合显著增加了辛伐他汀的血清浓度,导致横纹肌溶解症。

新发现和结论

对于与非典型 CYP 抑制剂相关的他汀类药物引起的肌病患者,应考虑进行基因检测和替代他汀类药物,以降低未来相互作用的风险。

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