Department of Pharmacy Practice, Lipscomb University College of Pharmacy, Nashville, TN, USA.
Department of Pharmacy, Deaconess Health System, Evansville, IN, USA.
J Clin Pharm Ther. 2021 Jun;46(3):853-855. doi: 10.1111/jcpt.13327. Epub 2020 Dec 5.
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.
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.
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.
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。
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。
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。