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Robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases

The fundament of an evidence-based severity assessment in laboratory animal science is reliable distress parameters. Many readouts are used to evaluate and determine animal distress and the severity of experimental procedures. Therefore, we analyzed four distinct parameters like the body weight, bur...

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Autores principales: Talbot, Steven R., Kumstel, Simone, Schulz, Benjamin, Tang, Guanglin, Abdelrahman, Ahmed, Seume, Nico, Wendt, Edgar H. U., Eichberg, Johanna, Häger, Christine, Bleich, André, Vollmar, Brigitte, Zechner, Dietmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929045/
https://www.ncbi.nlm.nih.gov/pubmed/36788346
http://dx.doi.org/10.1038/s41598-023-29623-8
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author Talbot, Steven R.
Kumstel, Simone
Schulz, Benjamin
Tang, Guanglin
Abdelrahman, Ahmed
Seume, Nico
Wendt, Edgar H. U.
Eichberg, Johanna
Häger, Christine
Bleich, André
Vollmar, Brigitte
Zechner, Dietmar
author_facet Talbot, Steven R.
Kumstel, Simone
Schulz, Benjamin
Tang, Guanglin
Abdelrahman, Ahmed
Seume, Nico
Wendt, Edgar H. U.
Eichberg, Johanna
Häger, Christine
Bleich, André
Vollmar, Brigitte
Zechner, Dietmar
author_sort Talbot, Steven R.
collection PubMed
description The fundament of an evidence-based severity assessment in laboratory animal science is reliable distress parameters. Many readouts are used to evaluate and determine animal distress and the severity of experimental procedures. Therefore, we analyzed four distinct parameters like the body weight, burrowing behavior, nesting, and distress score in the four gastrointestinal animal models (pancreatic ductal adenocarcinoma (PDA), pancreatitis, CCl(4) intoxication, and bile duct ligation (BDL)). Further, we determined the parameters’ robustness in various experimental subgroups due to slight variations like drug treatment or telemeter implantations. We used non-parametric bootstrapping to get robust estimates and 95% confidence intervals for the experimental groups. It was found that the performance of the readout parameters is model-dependent and that the distress score is prone to experimental variation. On the other hand, we also found that burrowing and nesting can be more robust than, e.g., the body weight when evaluating PDA. However, the body weight still was highly robust in BDL, pancreatitis, and CCl(4) intoxication. To address the complex nature of the multi-dimensional severity space, we used the Relative Severity Assessment (RELSA) procedure to combine multiple distress parameters into a score and mapped the subgroups and models against a defined reference set obtained by telemeter implantation. This approach allowed us to compare the severity of individual animals in the experimental subgroups using the maximum achieved severity (RELSA(max)). With this, the following order of severity was found for the animal models: CCl(4) < PDA ≈ Pancreatitis < BDL. Furthermore, the robustness of the RELSA procedure and outcome was externally validated with a reference set from another laboratory also obtained from telemeter implantation. Since the RELSA procedure reflects the multi-dimensional severity information and is highly robust in estimating the quantitative severity within and between models, it can be deemed a valuable tool for laboratory animal severity assessment.
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spelling pubmed-99290452023-02-16 Robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases Talbot, Steven R. Kumstel, Simone Schulz, Benjamin Tang, Guanglin Abdelrahman, Ahmed Seume, Nico Wendt, Edgar H. U. Eichberg, Johanna Häger, Christine Bleich, André Vollmar, Brigitte Zechner, Dietmar Sci Rep Article The fundament of an evidence-based severity assessment in laboratory animal science is reliable distress parameters. Many readouts are used to evaluate and determine animal distress and the severity of experimental procedures. Therefore, we analyzed four distinct parameters like the body weight, burrowing behavior, nesting, and distress score in the four gastrointestinal animal models (pancreatic ductal adenocarcinoma (PDA), pancreatitis, CCl(4) intoxication, and bile duct ligation (BDL)). Further, we determined the parameters’ robustness in various experimental subgroups due to slight variations like drug treatment or telemeter implantations. We used non-parametric bootstrapping to get robust estimates and 95% confidence intervals for the experimental groups. It was found that the performance of the readout parameters is model-dependent and that the distress score is prone to experimental variation. On the other hand, we also found that burrowing and nesting can be more robust than, e.g., the body weight when evaluating PDA. However, the body weight still was highly robust in BDL, pancreatitis, and CCl(4) intoxication. To address the complex nature of the multi-dimensional severity space, we used the Relative Severity Assessment (RELSA) procedure to combine multiple distress parameters into a score and mapped the subgroups and models against a defined reference set obtained by telemeter implantation. This approach allowed us to compare the severity of individual animals in the experimental subgroups using the maximum achieved severity (RELSA(max)). With this, the following order of severity was found for the animal models: CCl(4) < PDA ≈ Pancreatitis < BDL. Furthermore, the robustness of the RELSA procedure and outcome was externally validated with a reference set from another laboratory also obtained from telemeter implantation. Since the RELSA procedure reflects the multi-dimensional severity information and is highly robust in estimating the quantitative severity within and between models, it can be deemed a valuable tool for laboratory animal severity assessment. Nature Publishing Group UK 2023-02-14 /pmc/articles/PMC9929045/ /pubmed/36788346 http://dx.doi.org/10.1038/s41598-023-29623-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Talbot, Steven R.
Kumstel, Simone
Schulz, Benjamin
Tang, Guanglin
Abdelrahman, Ahmed
Seume, Nico
Wendt, Edgar H. U.
Eichberg, Johanna
Häger, Christine
Bleich, André
Vollmar, Brigitte
Zechner, Dietmar
Robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases
title Robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases
title_full Robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases
title_fullStr Robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases
title_full_unstemmed Robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases
title_short Robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases
title_sort robustness of a multivariate composite score when evaluating distress of animal models for gastrointestinal diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929045/
https://www.ncbi.nlm.nih.gov/pubmed/36788346
http://dx.doi.org/10.1038/s41598-023-29623-8
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