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使用AIC权重进行模型平均以进行低剂量兴奋效应的假设检验。

Model Averaging with AIC Weights for Hypothesis Testing of Hormesis at Low Doses.

作者信息

Kim Steven B, Sanders Nathan

机构信息

Department of Mathematics and Statistics, California State University, Monterey Bay, Seaside, CA, USA.

出版信息

Dose Response. 2017 Jun 29;15(2):1559325817715314. doi: 10.1177/1559325817715314. eCollection 2017 Apr-Jun.

DOI:10.1177/1559325817715314
PMID:28694745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5495511/
Abstract

For many dose-response studies, large samples are not available. Particularly, when the outcome of interest is binary rather than continuous, a large sample size is required to provide evidence for hormesis at low doses. In a small or moderate sample, we can gain statistical power by the use of a parametric model. It is an efficient approach when it is correctly specified, but it can be misleading otherwise. This research is motivated by the fact that data points at high experimental doses have too much contribution in the hypothesis testing when a parametric model is misspecified. In dose-response analyses, to account for model uncertainty and to reduce the impact of model misspecification, averaging multiple models have been widely discussed in the literature. In this article, we propose to average semiparametric models when we test for hormesis at low doses. We show the different characteristics of averaging parametric models and averaging semiparametric models by simulation. We apply the proposed method to real data, and we show that values from averaged semiparametric models are more credible than values from averaged parametric methods. When the true dose-response relationship does not follow a parametric assumption, the proposed method can be an alternative robust approach.

摘要

对于许多剂量反应研究而言,无法获得大样本。特别是,当感兴趣的结果是二元而非连续的时,需要大样本量才能为低剂量时的 hormesis 提供证据。在小样本或中等样本中,我们可以通过使用参数模型来提高统计功效。如果正确设定,这是一种有效的方法,但否则可能会产生误导。本研究的动机是,当参数模型设定错误时,高实验剂量的数据点在假设检验中贡献过大。在剂量反应分析中,为了考虑模型不确定性并减少模型设定错误的影响,文献中广泛讨论了对多个模型进行平均的方法。在本文中,我们建议在低剂量时检验 hormesis 时对半参数模型进行平均。我们通过模拟展示了平均参数模型和平均半参数模型的不同特征。我们将所提出的方法应用于实际数据,并表明平均半参数模型的值比平均参数方法的值更可信。当真实的剂量反应关系不遵循参数假设时,所提出的方法可以是一种替代的稳健方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/7c7f6b1401bd/10.1177_1559325817715314-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/17d38e8af12f/10.1177_1559325817715314-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/0688f49615b6/10.1177_1559325817715314-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/85dff4df1804/10.1177_1559325817715314-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/7c7f6b1401bd/10.1177_1559325817715314-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/17d38e8af12f/10.1177_1559325817715314-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/0688f49615b6/10.1177_1559325817715314-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/85dff4df1804/10.1177_1559325817715314-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d38c/5495511/7c7f6b1401bd/10.1177_1559325817715314-fig4.jpg

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本文引用的文献

1
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Biostatistics. 2016 Jul;17(3):523-36. doi: 10.1093/biostatistics/kxw004. Epub 2016 Feb 12.
2
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3
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4
Generic Hockey-Stick Model for Estimating Benchmark Dose and Potency: Performance Relative to BMDS and Application to Anthraquinone.用于估计基准剂量和效价的通用冰球模型:与 BMDS 的相对性能及在蒽醌中的应用
Dose Response. 2011;9(2):182-208. doi: 10.2203/dose-response.10-018.Bogen. Epub 2010 Oct 21.
5
Potential uncertainty reduction in model-averaged benchmark dose estimates informed by an additional dose study.基于额外剂量研究的模型平均基准剂量估计的潜在不确定性降低。
Risk Anal. 2011 Oct;31(10):1561-75. doi: 10.1111/j.1539-6924.2011.01595.x. Epub 2011 Mar 9.
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Modeling nonlinear dose-response relationships in epidemiologic studies: statistical approaches and practical challenges.流行病学研究中非线性剂量-反应关系的建模:统计方法和实际挑战。
Dose Response. 2006 May 22;3(4):474-90. doi: 10.2203/dose-response.003.04.004.
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Hormesis defined.毒物兴奋效应的定义。
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Model uncertainty and risk estimation for experimental studies of quantal responses.量子反应实验研究的模型不确定性与风险估计
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