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Evaluating the Use of Linear Mixed-Effect Models for Inference of the Concentration-QTc Slope Estimate as a Surrogate for a Biological QTc Model

机译:评估使用线性混合效应模型推断浓度-QTc斜率估计值作为生物QTc模型的替代物

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摘要

In concentration-QTc modeling, oscillatory functions have been used to characterize biological rhythms in QTc profiles. Fitting such functions is not always feasible because it requires sufficient electrocardiograph sampling. In this study, drug concentration and QTc data were simulated using a published biological QTc model (oscillatory functions). Then, linear mixed-effect models and the biological model were fitted and evaluated in terms of biases, precisions, and qualities of inferences. The simpler linear mixed-effect model with day and time as a factor variables provided similar accuracy of the concentration-QTc slope estimates to the complex biological model and was able to accurately predict the drug-induced QTc prolongation with less than 1 ms bias, despite its empirical nature to account for biological rhythm. The current study may guide a concentration-QTc modeling strategy that can be easily prespecified, does not suffer from poor convergence, and achieves little bias in drug-induced QTc estimates.
机译:在浓度-QTc建模中,振荡功能已被用来表征QTc谱中的生物节律。装配此类功能并不总是可行的,因为它需要足够的心电图仪采样。在这项研究中,使用公开的生物学QTc模型(振荡功能)模拟药物浓度和QTc数据。然后,拟合线性混合效应模型和生物学模型,并根据偏差,精确度和推断质量进行评估。以天和时间为因子变量的简单线性混合效应模型,提供了与复杂生物学模型相似的浓度-QTc斜率估算值的准确性,并且尽管偏差小于1 ms,也能够准确预测药物诱导的QTc延长它的经验性质可以解释生物节律。当前的研究可以指导一种浓度-QTc建模策略,该策略可以很容易地预先设定,不会出现不良收敛,并且在药物诱导的QTc估计中几乎没有偏差。

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