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Monotonic Bayesian Semiparametric Benchmark Dose Analysis

机译:单调贝叶斯半参数基准剂量分析

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Quantitative risk assessment proceeds by first estimating a dose-response model and then inverting this model to estimate the dose that corresponds to some prespecified level of response. The parametric form of the dose-response model often plays a large role in determining this dose. Consequently, the choice of the proper model is a major source of uncertainty when estimating such endpoints. While methods exist that attempt to incorporate the uncertainty by forming an estimate based upon all models considered, such methods may fail when the true model is on the edge of the space of models considered and cannot be formed from a weighted sum of constituent models. We propose a semiparametric model for dose-response data as well as deriving a dose estimate associated with a particular response. In this model formulation, the only restriction on the model form is that it is monotonic. We use this model to estimate the dose-response curve from a long-term cancer bioassay, as well as compare this to methods currently used to account for model uncertainty. A small simulation study is conducted showing that the method is superior to model averaging when estimating exposure that arises from a quantal-linear dose-response mechanism, and is similar to these methods when investigating nonlinear dose-response patterns.
机译:通过首先估计剂量反应模型,然后反转该模型以估计对应于某些预先指定的反应水平的剂量,进行定量风险评估。剂量反应模型的参数形式通常在确定此剂量中起很大作用。因此,在估算此类端点时,选择合适的模型是不确定性的主要来源。虽然存在尝试通过基于所考虑的所有模型形成估计来合并不确定性的方法,但是当真实模型位于所考虑的模型空间的边缘并且无法由组成模型的加权和形成时,此类方法可能会失败。我们提出用于剂量反应数据的半参数模型,以及推导与特定反应相关的剂量估计。在此模型公式中,对模型形式的唯一限制是它是单调的。我们使用该模型来评估长期癌症生物测定的剂量反应曲线,并将其与当前用于解释模型不确定性的方法进行比较。进行了一次小型模拟研究,结果表明,该方法在估计由定量线性剂量反应机制引起的暴露时优于模型平均,并且在研究非线性剂量反应模式时类似于这些方法。

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