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Auto-Generated Physiological Chain Data for an Ontological Framework for Pharmacology and Mechanism of Action to Determine Suspected Drugs in Cases of Dysuria

机译:用于药理学的本体生理链数据和作用机制,以确定疑似药物的疑似药物

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Introduction Patients often take several different medications for multiple conditions concurrently. Therefore, when adverse drug events (ADEs) occur, it is necessary to consider the mechanisms responsible. Few approaches consider the mechanisms of ADEs, such as changes in physiological states. We proposed that the ontological framework for pharmacology and mechanism of action (pharmacodynamics) we developed could be used for this approach. However, the existing knowledge base contains little data on physiological chains (PCs). Objective We aimed to investigate a method for automatically generating missing PC from the viewpoint of anatomical structures. This study was conducted to determine dysuria-related adverse events more likely to occur during multidrug administration. Methods We adopted a systematic approach to determine drugs suspected to cause adverse events and incorporated existing data and data generated in our newly developed method into our ontological framework. The performance of automated data generation was evaluated using this newly developed system. Suspected drugs determined by the system were compared with those derived from adverse events databases. Results Of the 242 drugs involving suspected drug-induced urinary retention or dysuria, 26 suspected drugs were determined. Of these, five were drugs with side effects not listed in drug package inserts. The system derived potential mechanisms of action, PCs, and suspected drugs. Conclusion Our method is novel in that it generates PC data from anatomical structural properties and could serve as a knowledge base for determining suspected drugs by potential mechanisms of action.
机译:引言患者通常同时服用多种不同的药物。因此,当发生不良药物事件(ades)时,有必要考虑负责的机制。很少有方法考虑ades的机制,例如生理状态的变化。我们建议我们开发的药理和作用机制(药效学)的本体论框架可用于这种方法。但是,现有知识库包含生理链(PC)的少数数据。目的我们旨在调查从解剖结构的观点来看一种自动生成缺失的PC的方法。该研究进行了在多药给药期间确定困难相关的不良事件。方法采用了一种系统的方法来确定怀疑造成不良事件的药物,并将新开发方法生成的现有数据和数据纳入我们的本体论框架。使用该新开发的系统评估自动数据生成的性能。将系统测定的疑似药物与来自不良事件数据库的那些进行比较。确定了涉及疑似药物诱导的尿潴留的242种药物,26例疑似药物的药物。其中,五种是药物包装插入物中未列出副作用的药物。系统导出潜在的作用机制,PC和疑似药物。结论我们的方法是新颖的,因为它产生了来自解剖结构特性的PC数据,可以作为通过潜在的作用机制来确定可疑药物的知识库。

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