ArticleRegulatory toxicology and pharmacology : RTP2023
An investigation of non-informative priors for Bayesian dose-response modeling.
Article in Regulatory toxicology and pharmacology : RTP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed.
- A Method to Calibrate Chemical-Agnostic Quantitative Adverse Outcome Pathways on Multiple Chemical Data.Chemical research in toxicology · 2026Article
- Cold water immersion protocol optimization across exercise modalities: a systematic review and network meta-analysis of resistance training, endurance exercise, and team sport applications.BMC sports science, medicine & rehabilitation · 2026Article
- Bayesian statistical concepts with examples from rodent toxicology studies.Laboratory animals · 2024Review
- Reflected generalized concentration addition and Bayesian hierarchical models to improve chemical mixture prediction.PloS one · 2024Article
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Abstract
Toxicology analyses are built around dose-response modeling, and increasingly these methodologies utilize Bayesian estimation techniques. Bayesian estimation is unique because it includes prior distributional information in the analysis, which may impact the dose-response estimate meaningfully. As such analyses are often used for human health risk assessment, the practitioner must understand the impact of adding prior information to the dose-response study. One proposal in the literature is the use of the flat uniform prior distribution, which places a uniform prior probability over the dose-response model's parameters for a chosen range of values. Though the motivation of such a prior distribution is laudable in that it is most like maximum likelihood estimation seeking unbiased estimates of the dose-response, one can show that such priors add information and may introduce unexpected biases into the analysis. This manuscript shows through numerous empirical examples why prior distributions that are non-informative across all endpoints of interest do not exist for dose-response models; that is, other quantities of interest will be informed by choosing one inferential quantity not informed.
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