Guidance on the use of the benchmark dose approach in risk assessment. (25th October 2022)
- Record Type:
- Journal Article
- Title:
- Guidance on the use of the benchmark dose approach in risk assessment. (25th October 2022)
- Main Title:
- Guidance on the use of the benchmark dose approach in risk assessment
- Authors:
- More, Simon John
Bampidis, Vasileios
Benford, Diane
Bragard, Claude
Halldorsson, Thorhallur Ingi
Hernández‐Jerez, Antonio F
Bennekou, Susanne Hougaard
Koutsoumanis, Kostas
Lambré, Claude
Machera, Kyriaki
Mennes, Wim
Mullins, Ewen
Nielsen, Søren Saxmose
Schrenk, Dieter
Turck, Dominique
Younes, Maged
Aerts, Marc
Edler, Lutz
Sand, Salomon
Wright, Matthew
Binaglia, Marco
Bottex, Bernard
Abrahantes, Jose Cortiñas
Schlatter, Josef - Abstract:
- Abstract: The Scientific Committee (SC) reconfirms that the benchmark dose (BMD) approach is a scientifically more advanced method compared to the no‐observed‐adverse‐effect‐level (NOAEL) approach for deriving a Reference Point (RP). The major change compared to the previous Guidance (EFSA SC, 2017) concerns the Section 2.5, in which a change from the frequentist to the Bayesian paradigm is recommended. In the former, uncertainty about the unknown parameters is measured by confidence and significance levels, interpreted and calibrated under hypothetical repetition, while probability distributions are attached to the unknown parameters in the Bayesian approach, and the notion of probability is extended to reflect uncertainty of knowledge. In addition, the Bayesian approach can mimic a learning process and reflects the accumulation of knowledge over time. Model averaging is again recommended as the preferred method for estimating the BMD and calculating its credible interval. The set of default models to be used for BMD analysis has been reviewed and amended so that there is now a single set of models for quantal and continuous data. The flow chart guiding the reader step‐by‐step when performing a BMD analysis has also been updated, and a chapter comparing the frequentist to the Bayesian paradigm inserted. Also, when using Bayesian BMD modelling, the lower bound (BMDL) is to be considered as potential RP, and the upper bound (BMDU) is needed for establishing the BMDU/BMDLAbstract: The Scientific Committee (SC) reconfirms that the benchmark dose (BMD) approach is a scientifically more advanced method compared to the no‐observed‐adverse‐effect‐level (NOAEL) approach for deriving a Reference Point (RP). The major change compared to the previous Guidance (EFSA SC, 2017) concerns the Section 2.5, in which a change from the frequentist to the Bayesian paradigm is recommended. In the former, uncertainty about the unknown parameters is measured by confidence and significance levels, interpreted and calibrated under hypothetical repetition, while probability distributions are attached to the unknown parameters in the Bayesian approach, and the notion of probability is extended to reflect uncertainty of knowledge. In addition, the Bayesian approach can mimic a learning process and reflects the accumulation of knowledge over time. Model averaging is again recommended as the preferred method for estimating the BMD and calculating its credible interval. The set of default models to be used for BMD analysis has been reviewed and amended so that there is now a single set of models for quantal and continuous data. The flow chart guiding the reader step‐by‐step when performing a BMD analysis has also been updated, and a chapter comparing the frequentist to the Bayesian paradigm inserted. Also, when using Bayesian BMD modelling, the lower bound (BMDL) is to be considered as potential RP, and the upper bound (BMDU) is needed for establishing the BMDU/BMDL ratio reflecting the uncertainty in the BMD estimate. This updated guidance does not call for a general re‐evaluation of previous assessments where the NOAEL approach or the BMD approach as described in the 2009 or 2017 Guidance was used, in particular when the exposure is clearly lower (e.g. more than one order of magnitude) than the health‐based guidance value. Finally, the SC firmly reiterates to reconsider test guidelines given the wide application of the BMD approach. Abstract : This publication is linked to the following EFSA Supporting Publications article: http://onlinelibrary.wiley.com/doi/10.2903/sp.efsa.2022.EN-7585/full … (more)
- Is Part Of:
- EFSA journal. Volume 20:Number 10(2022)
- Journal:
- EFSA journal
- Issue:
- Volume 20:Number 10(2022)
- Issue Display:
- Volume 20, Issue 10 (2022)
- Year:
- 2022
- Volume:
- 20
- Issue:
- 10
- Issue Sort Value:
- 2022-0020-0010-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-10-25
- Subjects:
- BMD -- BMDL -- benchmark response -- NOAEL -- dose–response modelling -- BMD software -- Bayesian model averaging
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363.19209405 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1831-4732 ↗
- DOI:
- 10.2903/j.efsa.2022.7584 ↗
- Languages:
- English
- ISSNs:
- 1831-4732
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library HMNTS - ELD Digital store
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- 24240.xml