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Identification and Mechanistic Investigation of Drug-Drug Interactions Associated With Myopathy: A Translational Approach

机译:与肌病相关的药物相互作用的鉴定和机理研究:一种转化方法

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摘要

Myopathy is a group of muscle diseases that can be induced or exacerbated by drug-drug interactions (DDIs). We sought to identify clinically important myopathic DDIs and elucidate their underlying mechanisms. Five DDIs were found to increase the risk of myopathy based on analysis of observational data from the Indiana Network of Patient Care. Loratadine interacted with simvastatin (relative risk 95% confidence interval [CI] = [1.39, 2.06]), alprazolam (1.50, 2.31), ropinirole (2.06, 5.00), and omeprazole (1.15, 1.38). Promethazine interacted with tegaserod (1.94, 4.64). In vitro investigation showed that these DDIs were unlikely to result from inhibition of drug metabolism by CYP450 enzymes or from inhibition of hepatic uptake via the membrane transporter OATP1B1/1B3. However, we did observe in vitro synergistic myotoxicity of simvastatin and desloratadine, suggesting a role in loratadine-simvastatin interaction. This interaction was epidemiologically confirmed (odds ratio 95% CI = [2.02, 3.65]) using the data from the US Food and Drug Administration Adverse Event Reporting System.
机译:肌病是一组肌肉疾病,可通过药物-药物相互作用(DDI)诱发或加重。我们试图确定临床上重要的肌病性DDI,并阐明其潜在机制。根据来自印第安那州患者护理网络的观察数据分析,发现五个DDI增加了患肌病的风险。氯雷他定与辛伐他汀(相对危险度95%置信区间[CI] == [1.39,2.06]),阿普唑仑(1.50,2.31),罗匹尼罗(2.06,5.00)和奥美拉唑(1.15,1.38)相互作用。异丙嗪与替加色罗相互作用(1.94,4.64)。体外研究表明,这些DDI不太可能是由于CYP450酶抑制药物代谢或经由膜转运蛋白OATP1B1 / 1B3抑制肝吸收而引起的。但是,我们确实观察到了辛伐他汀和去氯雷他定的体外协同肌毒性,提示其在氯雷他定与辛伐他汀的相互作用中起作用。使用美国食品和药物管理局不良事件报告系统的数据在流行病学上确认了这种相互作用(比值95%CI = [2.02,3.65])。

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