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Untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma

Feline chronic enteropathy (CE) is a common gastrointestinal disorder in cats and mainly comprises inflammatory bowel disease (IBD) and small cell lymphoma (SCL). Differentiation between IBD and SCL can be diagnostically challenging. We characterized the fecal metabolome of 14 healthy cats and 22 ca...

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Autores principales: Marsilio, Sina, Chow, Betty, Hill, Steve L., Ackermann, Mark R., Estep, J. Scot, Sarawichitr, Benjamin, Pilla, Rachel, Lidbury, Jonathan A., Steiner, Joerg M., Suchodolski, Jan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080598/
https://www.ncbi.nlm.nih.gov/pubmed/33911166
http://dx.doi.org/10.1038/s41598-021-88707-5
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author Marsilio, Sina
Chow, Betty
Hill, Steve L.
Ackermann, Mark R.
Estep, J. Scot
Sarawichitr, Benjamin
Pilla, Rachel
Lidbury, Jonathan A.
Steiner, Joerg M.
Suchodolski, Jan S.
author_facet Marsilio, Sina
Chow, Betty
Hill, Steve L.
Ackermann, Mark R.
Estep, J. Scot
Sarawichitr, Benjamin
Pilla, Rachel
Lidbury, Jonathan A.
Steiner, Joerg M.
Suchodolski, Jan S.
author_sort Marsilio, Sina
collection PubMed
description Feline chronic enteropathy (CE) is a common gastrointestinal disorder in cats and mainly comprises inflammatory bowel disease (IBD) and small cell lymphoma (SCL). Differentiation between IBD and SCL can be diagnostically challenging. We characterized the fecal metabolome of 14 healthy cats and 22 cats with naturally occurring CE (11 cats with IBD and 11 cats with SCL). Principal component analysis and heat map analysis showed distinct clustering between cats with CE and healthy controls. Random forest classification revealed good group prediction for healthy cats and cats with CE, with an overall out-of-bag error rate of 16.7%. Univariate analysis indicated that levels of 84 compounds in cats with CE differed from those in healthy cats. Polyunsaturated fatty acids held discriminatory power in differentiating IBD from SCL. Metabolomic profiles of cats with CE resembled those in people with CE with significant alterations of metabolites related to tryptophan, arachidonic acid, and glutathione pathways.
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spelling pubmed-80805982021-04-30 Untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma Marsilio, Sina Chow, Betty Hill, Steve L. Ackermann, Mark R. Estep, J. Scot Sarawichitr, Benjamin Pilla, Rachel Lidbury, Jonathan A. Steiner, Joerg M. Suchodolski, Jan S. Sci Rep Article Feline chronic enteropathy (CE) is a common gastrointestinal disorder in cats and mainly comprises inflammatory bowel disease (IBD) and small cell lymphoma (SCL). Differentiation between IBD and SCL can be diagnostically challenging. We characterized the fecal metabolome of 14 healthy cats and 22 cats with naturally occurring CE (11 cats with IBD and 11 cats with SCL). Principal component analysis and heat map analysis showed distinct clustering between cats with CE and healthy controls. Random forest classification revealed good group prediction for healthy cats and cats with CE, with an overall out-of-bag error rate of 16.7%. Univariate analysis indicated that levels of 84 compounds in cats with CE differed from those in healthy cats. Polyunsaturated fatty acids held discriminatory power in differentiating IBD from SCL. Metabolomic profiles of cats with CE resembled those in people with CE with significant alterations of metabolites related to tryptophan, arachidonic acid, and glutathione pathways. Nature Publishing Group UK 2021-04-28 /pmc/articles/PMC8080598/ /pubmed/33911166 http://dx.doi.org/10.1038/s41598-021-88707-5 Text en © The Author(s) 2021 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
Marsilio, Sina
Chow, Betty
Hill, Steve L.
Ackermann, Mark R.
Estep, J. Scot
Sarawichitr, Benjamin
Pilla, Rachel
Lidbury, Jonathan A.
Steiner, Joerg M.
Suchodolski, Jan S.
Untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma
title Untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma
title_full Untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma
title_fullStr Untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma
title_full_unstemmed Untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma
title_short Untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma
title_sort untargeted metabolomic analysis in cats with naturally occurring inflammatory bowel disease and alimentary small cell lymphoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080598/
https://www.ncbi.nlm.nih.gov/pubmed/33911166
http://dx.doi.org/10.1038/s41598-021-88707-5
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