Literature DB >> 12460753

Evaluation of the benchmark dose method for dichotomous data: model dependence and model selection.

Salomon Sand1, Agneta Falk Filipsson, Katarina Victorin.   

Abstract

The benchmark dose (BMD) method was evaluated using the USEPA BMD software. Dose-response data on cleft palate and hydronephrosis for a number of related polyhalogenated aromatic compounds were obtained from the literature. According to chi(2) test statistics, each dichotomous USEPA model failed to adequately describe only 1 of 12 cleft palate data sets. For hydronephrosis, the models were discriminated to a higher extent according to global goodness-of-fit. NOAELs for cleft palate corresponded to BMDLs (the approximate lower confidence limit on the BMD) for extra risks in the range of 5% or below. Model dependence of the BMDL estimate was more pronounced at lower levels of benchmark response (BMR). A BMR of 5% (extra risk) is recommended for cleft palate since model differences at this level were limited for all data. In addition, at BMRs of 5-10% the BMDL for all models was little affected by the specified confidence limit size (in the 90-99% range). For BMDL determination a conservative model selection approach was applied. At the suggested level of BMR (5%) this procedure resulted in use of the same model (multistage model) for the cleft palate endpoint in general. Akaike's information criterion (AIC) was considered for comparison between models. Determination of appropriateness of use of such methods in dose-response applications requires further analysis. Copyright 2002 Elsevier Science (USA)

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Year:  2002        PMID: 12460753     DOI: 10.1006/rtph.2002.1578

Source DB:  PubMed          Journal:  Regul Toxicol Pharmacol        ISSN: 0273-2300            Impact factor:   3.271


  9 in total

1.  On use of the multistage dose-response model for assessing laboratory animal carcinogenicity.

Authors:  Daniela K Nitcheva; Walter W Piegorsch; R Webster West
Journal:  Regul Toxicol Pharmacol       Date:  2007-03-25       Impact factor: 3.271

2.  Determination of the di-(2-ethylhexyl) phthalate NOAEL for reproductive development in the rat: importance of the retention of extra animals to adulthood.

Authors:  Chad R Blystone; Grace E Kissling; Jack B Bishop; Robert E Chapin; Gary W Wolfe; Paul M D Foster
Journal:  Toxicol Sci       Date:  2010-05-19       Impact factor: 4.849

3.  Model Selection and Estimation with Quantal-Response Data in Benchmark Risk Assessment.

Authors:  Edsel A Peña; Wensong Wu; Walter Piegorsch; Ronald W West; LingLing An
Journal:  Risk Anal       Date:  2016-06-20       Impact factor: 4.000

4.  The Impact of Model Uncertainty on Benchmark Dose Estimation.

Authors:  R Webster West; Walter W Piegorsch; Edsel A Peña; Lingling An; Wensong Wu; Alissa A Wickens; Hui Xiong; Wenhai Chen
Journal:  Environmetrics       Date:  2012-12       Impact factor: 1.900

5.  Translational benchmark risk analysis.

Authors:  Walter W Piegorsch
Journal:  J Risk Res       Date:  2010-07

6.  Confidence limits on one-stage model parameters in benchmark risk assessment.

Authors:  Brooke E Buckley; Walter W Piegorsch; R Webster West
Journal:  Environ Ecol Stat       Date:  2009-03-01       Impact factor: 1.119

7.  Statistical power considerations show the endocrine disruptor low-dose issue in a new light.

Authors:  Martin Scholze; Andreas Kortenkamp
Journal:  Environ Health Perspect       Date:  2007-12       Impact factor: 9.031

8.  Simulation-based assessment of model selection criteria during the application of benchmark dose method to quantal response data.

Authors:  Keita Yoshii; Hiroshi Nishiura; Kaoru Inoue; Takayuki Yamaguchi; Akihiko Hirose
Journal:  Theor Biol Med Model       Date:  2020-08-05       Impact factor: 2.432

Review 9.  Phthalate Exposure and Long-Term Epigenomic Consequences: A Review.

Authors:  Sudipta Dutta; Diana K Haggerty; Daniel A Rappolee; Douglas M Ruden
Journal:  Front Genet       Date:  2020-05-06       Impact factor: 4.772

  9 in total

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