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Development of a reference and proficiency chemical list for human steatosis endpoints in vitro

The most prevalent liver disease in humans is non-alcoholic fatty liver disease, characterised by excessive hepatic fat accumulation, or steatosis. The western diet and a sedentary lifestyle are considered to be major influences, but chemical exposure may also play a role. Suspected environmental ch...

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Autores principales: Kubickova, Barbara, Jacobs, Miriam N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166001/
https://www.ncbi.nlm.nih.gov/pubmed/37168981
http://dx.doi.org/10.3389/fendo.2023.1126880
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author Kubickova, Barbara
Jacobs, Miriam N.
author_facet Kubickova, Barbara
Jacobs, Miriam N.
author_sort Kubickova, Barbara
collection PubMed
description The most prevalent liver disease in humans is non-alcoholic fatty liver disease, characterised by excessive hepatic fat accumulation, or steatosis. The western diet and a sedentary lifestyle are considered to be major influences, but chemical exposure may also play a role. Suspected environmental chemicals of concern include pesticides, plasticizers, metals, and perfluorinated compounds. Here we present a detailed literature analysis of chemicals that may (or may not) be implicated in lipid accumulation in the liver, to provide a basis for developing and optimizing human steatosis-relevant in vitro test methods. Independently collated and reviewed reference and proficiency chemicals are needed to assist in the test method development where an assay is intended to ultimately be taken forward for OECD Test Guideline development purposes. The selection criteria and considerations required for acceptance of proficiency chemical selection for OECD Test Guideline development. (i.e., structural diversity, range of activity including negatives, relevant chemical sectors, global restrictions, etc.) is described herein. Of 160 chemicals initially screened for inclusion, 36 were prioritized for detailed review. Based on the selection criteria and a weight-of-evidence basis, 18 chemicals (9 steatosis inducers, 9 negatives), including some environmental chemicals of concern, were ranked as high priority chemicals to assist in vitro human steatosis test method optimisation and proficiency testing, and inform potential subsequent test method (pre-)validation.
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spelling pubmed-101660012023-05-09 Development of a reference and proficiency chemical list for human steatosis endpoints in vitro Kubickova, Barbara Jacobs, Miriam N. Front Endocrinol (Lausanne) Endocrinology The most prevalent liver disease in humans is non-alcoholic fatty liver disease, characterised by excessive hepatic fat accumulation, or steatosis. The western diet and a sedentary lifestyle are considered to be major influences, but chemical exposure may also play a role. Suspected environmental chemicals of concern include pesticides, plasticizers, metals, and perfluorinated compounds. Here we present a detailed literature analysis of chemicals that may (or may not) be implicated in lipid accumulation in the liver, to provide a basis for developing and optimizing human steatosis-relevant in vitro test methods. Independently collated and reviewed reference and proficiency chemicals are needed to assist in the test method development where an assay is intended to ultimately be taken forward for OECD Test Guideline development purposes. The selection criteria and considerations required for acceptance of proficiency chemical selection for OECD Test Guideline development. (i.e., structural diversity, range of activity including negatives, relevant chemical sectors, global restrictions, etc.) is described herein. Of 160 chemicals initially screened for inclusion, 36 were prioritized for detailed review. Based on the selection criteria and a weight-of-evidence basis, 18 chemicals (9 steatosis inducers, 9 negatives), including some environmental chemicals of concern, were ranked as high priority chemicals to assist in vitro human steatosis test method optimisation and proficiency testing, and inform potential subsequent test method (pre-)validation. Frontiers Media S.A. 2023-04-24 /pmc/articles/PMC10166001/ /pubmed/37168981 http://dx.doi.org/10.3389/fendo.2023.1126880 Text en Copyright © 2023 Kubickova and Jacobs https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Kubickova, Barbara
Jacobs, Miriam N.
Development of a reference and proficiency chemical list for human steatosis endpoints in vitro
title Development of a reference and proficiency chemical list for human steatosis endpoints in vitro
title_full Development of a reference and proficiency chemical list for human steatosis endpoints in vitro
title_fullStr Development of a reference and proficiency chemical list for human steatosis endpoints in vitro
title_full_unstemmed Development of a reference and proficiency chemical list for human steatosis endpoints in vitro
title_short Development of a reference and proficiency chemical list for human steatosis endpoints in vitro
title_sort development of a reference and proficiency chemical list for human steatosis endpoints in vitro
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166001/
https://www.ncbi.nlm.nih.gov/pubmed/37168981
http://dx.doi.org/10.3389/fendo.2023.1126880
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