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使用分数多项式进行微生物风险评估中的模型平均法。

Model averaging in microbial risk assessment using fractional polynomials.

作者信息

Namata Harriet, Aerts Marc, Faes Christel, Teunis Peter

机构信息

Hasselt University, Center for Statistics, Campus Diepenbeek, Agoralaan, Gebouw D, B 3590 Diepenbeek, Belgium.

出版信息

Risk Anal. 2008 Aug;28(4):891-905. doi: 10.1111/j.1539-6924.2008.01063.x. Epub 2008 Jun 28.

Abstract

The alleviation of food-borne diseases caused by microbial pathogen remains a great concern in order to ensure the well-being of the general public. The relation between the ingested dose of organisms and the associated infection risk can be studied using dose-response models. Traditionally, a model selected according to a goodness-of-fit criterion has been used for making inferences. In this article, we propose a modified set of fractional polynomials as competitive dose-response models in risk assessment. The article not only shows instances where it is not obvious to single out one best model but also illustrates that model averaging can best circumvent this dilemma. The set of candidate models is chosen based on biological plausibility and rationale and the risk at a dose common to all these models estimated using the selected models and by averaging over all models using Akaike's weights. In addition to including parameter estimation inaccuracy, like in the case of a single selected model, model averaging accounts for the uncertainty arising from other competitive models. This leads to a better and more honest estimation of standard errors and construction of confidence intervals for risk estimates. The approach is illustrated for risk estimation at low dose levels based on Salmonella typhi and Campylobacter jejuni data sets in humans. Simulation studies indicate that model averaging has reduced bias, better precision, and also attains coverage probabilities that are closer to the 95% nominal level compared to best-fitting models according to Akaike information criterion.

摘要

为确保公众健康,减轻由微生物病原体引起的食源性疾病仍是一个重大关切问题。可以使用剂量反应模型来研究摄入的生物体剂量与相关感染风险之间的关系。传统上,根据拟合优度标准选择的模型已被用于进行推断。在本文中,我们提出了一组经过修改的分数多项式作为风险评估中的竞争性剂量反应模型。本文不仅展示了在某些情况下难以选出一个最佳模型的实例,还说明了模型平均法能够最好地规避这一困境。候选模型集是基于生物学合理性和原理选择的,并且使用所选模型并通过使用赤池权重对所有模型进行平均来估计所有这些模型共有的剂量下的风险。除了像在单个选定模型的情况下那样考虑参数估计不准确之外,模型平均法还考虑了来自其他竞争性模型的不确定性。这导致对标准误差进行更好、更真实的估计,并为风险估计构建置信区间。基于人类伤寒沙门氏菌和空肠弯曲菌数据集,对低剂量水平下的风险估计方法进行了说明。模拟研究表明,与根据赤池信息准则的最佳拟合模型相比,模型平均法减少了偏差,具有更好的精度,并且还达到了更接近95%名义水平的覆盖概率。

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