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首页> 外文期刊>CPT: Pharmacometrics & Systems Pharmacology >A Mixture Dose–Response Model for Identifying High‐Dimensional Drug Interaction Effects on Myopathy Using Electronic Medical Record Databases
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A Mixture Dose–Response Model for Identifying High‐Dimensional Drug Interaction Effects on Myopathy Using Electronic Medical Record Databases

机译:使用电子病历数据库识别高剂量药物相互作用对肌病的混合剂量反应模型

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摘要

AbstractInteractions between multiple drugs may yield excessive risk of adverse effects. This increased risk is not uniform for all combinations, although some combinations may have constant adverse effect risks. We developed a statistical model using medical record data to identify drug combinations that induce myopathy risk. Such combinations are revealed using a novel mixture model, comprised of a constant risk model and a dose–response risk model. The dose represents the number of drug combinations. Using an empirical Bayes estimation method, we successfully identified high-dimensional (two to six) drug combinations that are associated with excessive myopathy risk at significantly low local false-discovery rates. From the curve of a dose–response model and high-dimensional drug interaction data, we observed that myopathy risk increases as the drug interaction dimension increases. This is the first time that such a dose–response relationship for high-dimensional drug interactions was observed and extracted from the medical record database.
机译:摘要多种药物之间的相互作用可能产生过多的不良反应风险。尽管某些组合可能具有恒定的不良反应风险,但对于所有组合而言,这种增加的风险并不统一。我们使用病历数据开发了一种统计模型,以识别引起肌病风险的药物组合。使用新颖的混合模型可以揭示这种组合,该模型包括恒定风险模型和剂量反应风险模型。剂量代表药物组合的数量。使用经验贝叶斯估计方法,我们成功地识别了高维度(两到六种)药物组合,这些药物组合与过度肌病风险相关且局部误发现率非常低。从剂量反应模型和高维药物相互作用数据的曲线,我们观察到肌病风险随药物相互作用维度的增加而增加。这是首次观察到这种与高维药物相互作用的剂量反应关系,并从病历数据库中提取了这种关系。

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