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Reconstruction of Exposure to m-Xylene from Human Biomonitoring Data Using PBPK Modelling, Bayesian Inference, and Markov Chain Monte Carlo Simulation

机译:使用PBPK模型,贝叶斯推断和马尔可夫链蒙特卡洛模拟法从人类生物监测数据重建间二甲苯的暴露量

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摘要

There are numerous biomonitoring programs, both recent and ongoing, to evaluate environmental exposure of humans to chemicals. Due to the lack of exposure and kinetic data, the correlation of biomarker levels with exposure concentrations leads to difficulty in utilizing biomonitoring data for biological guidance values. Exposure reconstruction or reverse dosimetry is the retrospective interpretation of external exposure consistent with biomonitoring data. We investigated the integration of physiologically based pharmacokinetic modelling, global sensitivity analysis, Bayesian inference, and Markov chain Monte Carlo simulation to obtain a population estimate of inhalation exposure to m-xylene. We used exhaled breath and venous blood m-xylene and urinary 3-methylhippuric acid measurements from a controlled human volunteer study in order to evaluate the ability of our computational framework to predict known inhalation exposures. We also investigated the importance of model structure and dimensionality with respect to its ability to reconstruct exposure.
机译:最近和正在进行的生物监测计划很多,用于评估人类对化学物质的环境暴露。由于缺乏暴露和动力学数据,生物标志物水平与暴露浓度的相关性导致难以将生物监测数据用于生物学指导值。暴露重建或反向剂量测定是对与生物监测数据一致的外部暴露的回顾性解释。我们研究了基于生理学的药代动力学建模,全局敏感性分析,贝叶斯推断和马尔可夫链蒙特卡洛模拟的集成,以获得对间二甲苯吸入暴露的总体估计。为了评估我们的计算框架预测已知吸入暴露的能力,我们使用了一项来自受控人类志愿者研究的呼气和静脉血间二甲苯和尿液中的3-甲基马尿酸测量值。我们还研究了模型结构和维度相对于其重构曝光能力的重要性。

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