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Using semantics to scale up evidence-based chemical risk-assessments

BACKGROUND: The manual processes used for risk assessments are not scaling to the amount of data available. Although automated approaches appear promising, they must be transparent in a public policy setting. OBJECTIVE: Our goal is to create an automated approach that moves beyond retrieval to the e...

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Autores principales: Blake, Catherine, Flaws, Jodi A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673667/
https://www.ncbi.nlm.nih.gov/pubmed/34910747
http://dx.doi.org/10.1371/journal.pone.0260712
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author Blake, Catherine
Flaws, Jodi A.
author_facet Blake, Catherine
Flaws, Jodi A.
author_sort Blake, Catherine
collection PubMed
description BACKGROUND: The manual processes used for risk assessments are not scaling to the amount of data available. Although automated approaches appear promising, they must be transparent in a public policy setting. OBJECTIVE: Our goal is to create an automated approach that moves beyond retrieval to the extraction step of the information synthesis process, where evidence is characterized as supporting, refuting, or neutral with respect to a given outcome. METHODS: We combine knowledge resources and natural language processing to resolve coordinated ellipses and thus avoid surface level differences between concepts in an ontology and outcomes in an abstract. As with a systematic review, the search criterion, and inclusion and exclusion criterion are explicit. RESULTS: The system scales to 482K abstracts on 27 chemicals. Results for three endpoints that are critical for cancer risk assessments show that refuting evidence (where the outcome decreased) was higher for cell proliferation (45.9%), and general cell changes (37.7%) than for cell death (25.0%). Moreover, cell death was the only end point where supporting claims were the majority (61.3%). If the number of abstracts that measure an outcome was used as a proxy for association there would be a stronger association with cell proliferation than cell death (20/27 chemicals). However, if the amount of supporting evidence was used (where the outcome increased) the conclusion would change for 21/27 chemicals (20 from proliferation to death and 1 from death to proliferation). CONCLUSIONS: We provide decision makers with a visual representation of supporting, neutral, and refuting evidence whilst maintaining the reproducibility and transparency needed for public policy. Our findings show that results from the retrieval step where the number of abstracts that measure an outcome are reported can be misleading if not accompanied with results from the extraction step where the directionality of the outcome is established.
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spelling pubmed-86736672021-12-16 Using semantics to scale up evidence-based chemical risk-assessments Blake, Catherine Flaws, Jodi A. PLoS One Research Article BACKGROUND: The manual processes used for risk assessments are not scaling to the amount of data available. Although automated approaches appear promising, they must be transparent in a public policy setting. OBJECTIVE: Our goal is to create an automated approach that moves beyond retrieval to the extraction step of the information synthesis process, where evidence is characterized as supporting, refuting, or neutral with respect to a given outcome. METHODS: We combine knowledge resources and natural language processing to resolve coordinated ellipses and thus avoid surface level differences between concepts in an ontology and outcomes in an abstract. As with a systematic review, the search criterion, and inclusion and exclusion criterion are explicit. RESULTS: The system scales to 482K abstracts on 27 chemicals. Results for three endpoints that are critical for cancer risk assessments show that refuting evidence (where the outcome decreased) was higher for cell proliferation (45.9%), and general cell changes (37.7%) than for cell death (25.0%). Moreover, cell death was the only end point where supporting claims were the majority (61.3%). If the number of abstracts that measure an outcome was used as a proxy for association there would be a stronger association with cell proliferation than cell death (20/27 chemicals). However, if the amount of supporting evidence was used (where the outcome increased) the conclusion would change for 21/27 chemicals (20 from proliferation to death and 1 from death to proliferation). CONCLUSIONS: We provide decision makers with a visual representation of supporting, neutral, and refuting evidence whilst maintaining the reproducibility and transparency needed for public policy. Our findings show that results from the retrieval step where the number of abstracts that measure an outcome are reported can be misleading if not accompanied with results from the extraction step where the directionality of the outcome is established. Public Library of Science 2021-12-15 /pmc/articles/PMC8673667/ /pubmed/34910747 http://dx.doi.org/10.1371/journal.pone.0260712 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Blake, Catherine
Flaws, Jodi A.
Using semantics to scale up evidence-based chemical risk-assessments
title Using semantics to scale up evidence-based chemical risk-assessments
title_full Using semantics to scale up evidence-based chemical risk-assessments
title_fullStr Using semantics to scale up evidence-based chemical risk-assessments
title_full_unstemmed Using semantics to scale up evidence-based chemical risk-assessments
title_short Using semantics to scale up evidence-based chemical risk-assessments
title_sort using semantics to scale up evidence-based chemical risk-assessments
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673667/
https://www.ncbi.nlm.nih.gov/pubmed/34910747
http://dx.doi.org/10.1371/journal.pone.0260712
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