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A Bayesian Meta-Analysis on Published Sample Mean and Variance Pharmacokinetic Data with Application to Drug-Drug Interaction Prediction

机译:样本均值和方差药代动力学数据的贝叶斯元分析及其在药物相互作用预测中的应用

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In drug-drug interaction (DDI) research, a two-drug interaction is usually predicted by individual drug pharmacokinetics (PK). Although subject-specific drug concentration data from clinical PK studies on inhibitor or inducer and substrate PK are not usually published, sample mean plasma drug concentrations and their standard deviations have been routinely reported. Hence there is a great need for meta-analysis and DDI prediction using such summarized PK data. In this study, an innovative DDI prediction method based on a three-level hierarchical Bayesian meta-analysis model is developed. The three levels model sample means and variances, between-study variances, and prior distributions. Through a ketoconazle-midazolam example and simulations, we demonstrate that our meta-analysis model can not only estimate PK parameters with small bias but also recover their between-study and between-subject variances well. More importantly, the posterior distributions of PK parameters and their variance components allow us to predict DDI at both population-average and study-specific levels. We are also able to predict the DDI between-subject/study variance. These statistical predictions have never been investigated in DDI research. Our simulation studies show that our meta-analysis approach has small bias in PK parameter estimates and DDI predictions. Sensitivity analysis was conducted to investigate the influences of interaction PK parameters, such as the inhibition constant Ki, on the DDI prediction.
机译:在药物-药物相互作用(DDI)研究中,通常通过单个药物的药代动力学(PK)来预测两种药物的相互作用。尽管通常不发表有关抑制剂或诱导剂和底物PK的临床PK研究的受试者特异性药物浓度数据,但常规报道了样品平均血浆药物浓度及其标准偏差。因此,非常需要使用这样的汇总PK数据进行荟萃分析和DDI预测。在这项研究中,开发了一种创新的DDI预测方法,该方法基于三级分层贝叶斯元分析模型。这三个级别对样本均值和方差,研究间方差和先验分布进行建模。通过酮康唑-咪达唑仑的实例和模拟,我们证明了我们的荟萃分析模型不仅可以估计偏倚较小的PK参数,而且可以很好地恢复研究之间和受试者之间的差异。更重要的是,PK参数及其方差分量的后验分布使我们能够在总体平均水平和研究特定水平上预测DDI。我们还能够预测受试者之间/研究之间的DDI差异。这些统计预测从未在DDI研究中进行过研究。我们的模拟研究表明,我们的荟萃分析方法在PK参数估计和DDI预测中具有较小的偏差。进行敏感性分析以研究相互作用PK参数(例如抑制常数Ki)对DDI预测的影响。

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