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A Pragmatic Approach to Adverse Outcome Pathway Development and Evaluation

The adverse outcome pathway (AOP) framework provides a practical means for organizing scientific knowledge that can be used to infer cause-effect relationships between stressor events and toxicity outcomes in intact organisms. It has reached wide acceptance as a tool to aid chemical safety assessmen...

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Autores principales: Svingen, Terje, Villeneuve, Daniel L, Knapen, Dries, Panagiotou, Eleftheria Maria, Draskau, Monica Kam, Damdimopoulou, Pauliina, O’Brien, Jason M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633887/
https://www.ncbi.nlm.nih.gov/pubmed/34534351
http://dx.doi.org/10.1093/toxsci/kfab113
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author Svingen, Terje
Villeneuve, Daniel L
Knapen, Dries
Panagiotou, Eleftheria Maria
Draskau, Monica Kam
Damdimopoulou, Pauliina
O’Brien, Jason M
author_facet Svingen, Terje
Villeneuve, Daniel L
Knapen, Dries
Panagiotou, Eleftheria Maria
Draskau, Monica Kam
Damdimopoulou, Pauliina
O’Brien, Jason M
author_sort Svingen, Terje
collection PubMed
description The adverse outcome pathway (AOP) framework provides a practical means for organizing scientific knowledge that can be used to infer cause-effect relationships between stressor events and toxicity outcomes in intact organisms. It has reached wide acceptance as a tool to aid chemical safety assessment and regulatory toxicology by supporting a systematic way of predicting adverse health outcomes based on accumulated mechanistic knowledge. A major challenge for broader application of the AOP concept in regulatory toxicology, however, has been developing robust AOPs to a level where they are peer reviewed and accepted. This is because the amount of work required to substantiate the modular units of a complete AOP is considerable, to the point where it can take years from start to finish. To help alleviate this bottleneck, we propose a more pragmatic approach to AOP development whereby the focus becomes on smaller blocks. First, we argue that the key event relationship (KER) should be formally recognized as the core building block of knowledge assembly within the AOP knowledge base (AOP-KB), albeit framing them within full AOPs to ensure regulatory utility. Second, we argue that KERs should be developed using systematic review approaches, but only in cases where the underlying concept does not build on what is considered canonical knowledge. In cases where knowledge is considered canonical, rigorous systematic review approaches should not be required. It is our hope that these approaches will contribute to increasing the pace at which the AOP-KB is populated with AOPs with utility for chemical safety assessors and regulators.
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spelling pubmed-86338872021-12-01 A Pragmatic Approach to Adverse Outcome Pathway Development and Evaluation Svingen, Terje Villeneuve, Daniel L Knapen, Dries Panagiotou, Eleftheria Maria Draskau, Monica Kam Damdimopoulou, Pauliina O’Brien, Jason M Toxicol Sci Forum The adverse outcome pathway (AOP) framework provides a practical means for organizing scientific knowledge that can be used to infer cause-effect relationships between stressor events and toxicity outcomes in intact organisms. It has reached wide acceptance as a tool to aid chemical safety assessment and regulatory toxicology by supporting a systematic way of predicting adverse health outcomes based on accumulated mechanistic knowledge. A major challenge for broader application of the AOP concept in regulatory toxicology, however, has been developing robust AOPs to a level where they are peer reviewed and accepted. This is because the amount of work required to substantiate the modular units of a complete AOP is considerable, to the point where it can take years from start to finish. To help alleviate this bottleneck, we propose a more pragmatic approach to AOP development whereby the focus becomes on smaller blocks. First, we argue that the key event relationship (KER) should be formally recognized as the core building block of knowledge assembly within the AOP knowledge base (AOP-KB), albeit framing them within full AOPs to ensure regulatory utility. Second, we argue that KERs should be developed using systematic review approaches, but only in cases where the underlying concept does not build on what is considered canonical knowledge. In cases where knowledge is considered canonical, rigorous systematic review approaches should not be required. It is our hope that these approaches will contribute to increasing the pace at which the AOP-KB is populated with AOPs with utility for chemical safety assessors and regulators. Oxford University Press 2021-09-17 /pmc/articles/PMC8633887/ /pubmed/34534351 http://dx.doi.org/10.1093/toxsci/kfab113 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society of Toxicology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Forum
Svingen, Terje
Villeneuve, Daniel L
Knapen, Dries
Panagiotou, Eleftheria Maria
Draskau, Monica Kam
Damdimopoulou, Pauliina
O’Brien, Jason M
A Pragmatic Approach to Adverse Outcome Pathway Development and Evaluation
title A Pragmatic Approach to Adverse Outcome Pathway Development and Evaluation
title_full A Pragmatic Approach to Adverse Outcome Pathway Development and Evaluation
title_fullStr A Pragmatic Approach to Adverse Outcome Pathway Development and Evaluation
title_full_unstemmed A Pragmatic Approach to Adverse Outcome Pathway Development and Evaluation
title_short A Pragmatic Approach to Adverse Outcome Pathway Development and Evaluation
title_sort pragmatic approach to adverse outcome pathway development and evaluation
topic Forum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633887/
https://www.ncbi.nlm.nih.gov/pubmed/34534351
http://dx.doi.org/10.1093/toxsci/kfab113
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