Literature DB >> 35707326

A new method for determining the benchmark dose tolerable region and endpoint probabilities for toxicology experiments.

Naha J Farhat1, Edward L Boone2, David J Edwards2.   

Abstract

The increase of exposure to toxic materials and hazardous chemicals is a major concern due to the adverse effect on human health. Among the major concerns of toxicologists is to determine acceptable levels of exposure to hazardous substances. Current approaches often evaluate each endpoint and stressor individually. We propose a novel method to simultaneously determine the Benchmark Dose Tolerable Region (BMDTR) for multiple endpoint and multiple stressor studies by adopting a Bayesian approach. A main concern while assessing the combined toxicological effect of a chemical mixture is the anticipated type of the combined action (i.e. synergistic or antagonistic); thus it was essential to account for interaction effects to handle this situation, imposing more challenges due to the non-linearity of the tolerable region. The proposed method will be evaluated using two approaches, the first one using the estimated value of the posterior median and the second approach using all MCMC samples from the posterior distribution. Furthermore, we propose a new method to determine the endpoint probabilities for each endpoint, which reflects the importance of each endpoint in helping determining the boundaries of the benchmark dose tolerable region (BMDTR).
© 2019 Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  BMD; Bayesian model; synergistic and inhibitory effects; tolerable region

Year:  2019        PMID: 35707326      PMCID: PMC9042098          DOI: 10.1080/02664763.2019.1654985

Source DB:  PubMed          Journal:  J Appl Stat        ISSN: 0266-4763            Impact factor:   1.416


  7 in total

1.  Estimation of the benchmark dose by structural equation models.

Authors:  Esben Budtz-Jørgensen
Journal:  Biostatistics       Date:  2006-10-30       Impact factor: 5.899

2.  A system of models for the action of drugs applied singly or jointly to biological organisms.

Authors:  J R Ashford; J M Cobby
Journal:  Biometrics       Date:  1974-03       Impact factor: 2.571

3.  A new method for determining allowable daily intakes.

Authors:  K S Crump
Journal:  Fundam Appl Toxicol       Date:  1984-10

4.  General models for the joint action of mixtures of drugs.

Authors:  J R Ashford
Journal:  Biometrics       Date:  1981-09       Impact factor: 2.571

5.  Neurotoxicological and statistical analyses of a mixture of five organophosphorus pesticides using a ray design.

Authors:  V C Moser; M Casey; A Hamm; W H Carter; J E Simmons; C Gennings
Journal:  Toxicol Sci       Date:  2005-03-30       Impact factor: 4.849

6.  A comparison of two approaches to the construction of models for quantal responses to mixtures of drugs.

Authors:  R L Plackett; P S Hewlett
Journal:  Biometrics       Date:  1967-03       Impact factor: 2.571

Review 7.  Potential health impacts of hard water.

Authors:  Pallav Sengupta
Journal:  Int J Prev Med       Date:  2013-08
  7 in total

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