Your browser doesn't support javascript.
loading
Simulation-based assessment of model selection criteria during the application of benchmark dose method to quantal response data.
Yoshii, Keita; Nishiura, Hiroshi; Inoue, Kaoru; Yamaguchi, Takayuki; Hirose, Akihiko.
Affiliation
  • Yoshii K; Graduate School of Medicine, Hokkaido University, Kita 15 Jo Nishi 7 Chome, Kita-ku, Sapporo-shi, Hokkaido, 060-8638, Japan.
  • Nishiura H; Graduate School of Medicine, Hokkaido University, Kita 15 Jo Nishi 7 Chome, Kita-ku, Sapporo-shi, Hokkaido, 060-8638, Japan. nishiurah@med.hokudai.ac.jp.
  • Inoue K; CREST, Japan Science and Technology Agency, Honcho 4-1-8, Kawaguchi, Saitama, 332-0012, Japan. nishiurah@med.hokudai.ac.jp.
  • Yamaguchi T; Division of Risk Assessment, National Institute of Health Sciences, Kawasaki, Japan.
  • Hirose A; Graduate School of Medicine, Hokkaido University, Kita 15 Jo Nishi 7 Chome, Kita-ku, Sapporo-shi, Hokkaido, 060-8638, Japan.
Theor Biol Med Model ; 17(1): 13, 2020 08 05.
Article in En | MEDLINE | ID: mdl-32753042
BACKGROUND: To employ the benchmark dose (BMD) method in toxicological risk assessment, it is critical to understand how the BMD lower bound for reference dose calculation is selected following statistical fitting procedures of multiple mathematical models. The purpose of this study was to compare the performances of various combinations of model exclusion and selection criteria for quantal response data. METHODS: Simulation-based evaluation of model exclusion and selection processes was conducted by comparing validity, reliability, and other model performance parameters. Three different empirical datasets for different chemical substances were analyzed for the assessment, each having different characteristics of the dose-response pattern (i.e. datasets with rich information in high or low response rates, or approximately linear dose-response patterns). RESULTS: The best performing criteria of model exclusion and selection were different across the different datasets. Model averaging over the three models with the lowest three AIC (Akaike information criteria) values (MA-3) did not produce the worst performance, and MA-3 without model exclusion produced the best results among the model averaging. Model exclusion including the use of the Kolmogorov-Smirnov test in advance of model selection did not necessarily improve the validity and reliability of the models. CONCLUSIONS: If a uniform methodological suggestion for the guideline is required to choose the best performing model for exclusion and selection, our results indicate that using MA-3 is the recommended option whenever applicable.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Computer Simulation / Risk Assessment / Benchmarking / Dose-Response Relationship, Drug Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Theor Biol Med Model Journal subject: BIOLOGIA / MEDICINA Year: 2020 Type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Computer Simulation / Risk Assessment / Benchmarking / Dose-Response Relationship, Drug Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Theor Biol Med Model Journal subject: BIOLOGIA / MEDICINA Year: 2020 Type: Article Affiliation country: Japan