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Scale Reduction of a Systems Coagulation Model With an Application to Modeling Pharmacokinetic–Pharmacodynamic Data

机译:系统凝结模型的规模缩减及其在药代动力学-药效学数据建模中的应用

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摘要

Bridging systems biology and pharmacokinetics–pharmacodynamics has resulted in models that are highly complex and complicated. They usually contain large numbers of states and parameters and describe multiple input–output relationships. Based on any given data set relating to a specific input–output process, it is possible that some states of the system are either less important or have no influence at all. In this study, we explore a simplification of a systems pharmacology model of the coagulation network for use in describing the time course of fibrinogen recovery after a brown snake bite. The technique of proper lumping is used to simplify the 62-state systems model to a 5-state model that describes the brown snake venom–fibrinogen relationship while maintaining an appropriate mechanistic relationship. The simplified 5-state model explains the observed decline and recovery in fibrinogen concentrations well. The techniques used in this study can be applied to other multiscale models.
机译:桥接系统生物学和药代动力学-药效学已经建立了高度复杂和复杂的模型。它们通常包含大量状态和参数,并描述多个输入-输出关系。基于与特定输入输出过程有关的任何给定数据集,系统的某些状态可能不太重要或根本没有影响。在这项研究中,我们探索了凝血网络的系统药理模型的简化,用于描述棕色蛇咬伤后纤维蛋白原恢复的时间过程。适当的集总技术用于将62状态系统模型简化为5状态模型,该模型描述了棕色蛇毒与纤维蛋白原的关系,同时保持了适当的机械关系。简化的五态模型很好地解释了观察到的纤维蛋白原浓度的下降和恢复。本研究中使用的技术可以应用于其他多尺度模型。

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