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Metabolomic biomarkers correlating with hepatic lipidosis in dairy cows

BACKGROUND: Hepatic lipidosis or fatty liver disease is a major metabolic disorder of high-producing dairy cows that compromises animal performance and, hence, causes heavy economic losses worldwide. This syndrome, occurring during the critical transition from gestation to early lactation, leads to...

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Autores principales: Imhasly, Sandro, Naegeli, Hanspeter, Baumann, Sven, von Bergen, Martin, Luch, Andreas, Jungnickel, Harald, Potratz, Sarah, Gerspach, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048253/
https://www.ncbi.nlm.nih.gov/pubmed/24888604
http://dx.doi.org/10.1186/1746-6148-10-122
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author Imhasly, Sandro
Naegeli, Hanspeter
Baumann, Sven
von Bergen, Martin
Luch, Andreas
Jungnickel, Harald
Potratz, Sarah
Gerspach, Christian
author_facet Imhasly, Sandro
Naegeli, Hanspeter
Baumann, Sven
von Bergen, Martin
Luch, Andreas
Jungnickel, Harald
Potratz, Sarah
Gerspach, Christian
author_sort Imhasly, Sandro
collection PubMed
description BACKGROUND: Hepatic lipidosis or fatty liver disease is a major metabolic disorder of high-producing dairy cows that compromises animal performance and, hence, causes heavy economic losses worldwide. This syndrome, occurring during the critical transition from gestation to early lactation, leads to an impaired health status, decreased milk yield, reduced fertility and shortened lifetime. Because the prevailing clinical chemistry parameters indicate advanced liver damage independently of the underlying disease, currently, hepatic lipidosis can only be ascertained by liver biopsy. We hypothesized that the condition of fatty liver disease may be accompanied by an altered profile of endogenous metabolites in the blood of affected animals. RESULTS: To identify potential small-molecule biomarkers as a novel diagnostic alternative, the serum samples of diseased dairy cows were subjected to a targeted metabolomics screen by triple quadrupole mass spectrometry. A subsequent multivariate test involving principal component and linear discriminant analyses yielded 29 metabolites (amino acids, phosphatidylcholines and sphingomyelines) that, in conjunction, were able to distinguish between dairy cows with no hepatic lipidosis and those displaying different stages of the disorder. CONCLUSIONS: This proof-of-concept study indicates that metabolomic profiles, including both amino acids and lipids, distinguish hepatic lipidosis from other peripartal disorders and, hence, provide a promising new tool for the diagnosis of hepatic lipidosis. By generating insights into the molecular pathogenesis of hepatic lipidosis, metabolomics studies may also facilitate the prevention of this syndrome.
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spelling pubmed-40482532014-06-07 Metabolomic biomarkers correlating with hepatic lipidosis in dairy cows Imhasly, Sandro Naegeli, Hanspeter Baumann, Sven von Bergen, Martin Luch, Andreas Jungnickel, Harald Potratz, Sarah Gerspach, Christian BMC Vet Res Research Article BACKGROUND: Hepatic lipidosis or fatty liver disease is a major metabolic disorder of high-producing dairy cows that compromises animal performance and, hence, causes heavy economic losses worldwide. This syndrome, occurring during the critical transition from gestation to early lactation, leads to an impaired health status, decreased milk yield, reduced fertility and shortened lifetime. Because the prevailing clinical chemistry parameters indicate advanced liver damage independently of the underlying disease, currently, hepatic lipidosis can only be ascertained by liver biopsy. We hypothesized that the condition of fatty liver disease may be accompanied by an altered profile of endogenous metabolites in the blood of affected animals. RESULTS: To identify potential small-molecule biomarkers as a novel diagnostic alternative, the serum samples of diseased dairy cows were subjected to a targeted metabolomics screen by triple quadrupole mass spectrometry. A subsequent multivariate test involving principal component and linear discriminant analyses yielded 29 metabolites (amino acids, phosphatidylcholines and sphingomyelines) that, in conjunction, were able to distinguish between dairy cows with no hepatic lipidosis and those displaying different stages of the disorder. CONCLUSIONS: This proof-of-concept study indicates that metabolomic profiles, including both amino acids and lipids, distinguish hepatic lipidosis from other peripartal disorders and, hence, provide a promising new tool for the diagnosis of hepatic lipidosis. By generating insights into the molecular pathogenesis of hepatic lipidosis, metabolomics studies may also facilitate the prevention of this syndrome. BioMed Central 2014-06-02 /pmc/articles/PMC4048253/ /pubmed/24888604 http://dx.doi.org/10.1186/1746-6148-10-122 Text en Copyright © 2014 Imhasly et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Imhasly, Sandro
Naegeli, Hanspeter
Baumann, Sven
von Bergen, Martin
Luch, Andreas
Jungnickel, Harald
Potratz, Sarah
Gerspach, Christian
Metabolomic biomarkers correlating with hepatic lipidosis in dairy cows
title Metabolomic biomarkers correlating with hepatic lipidosis in dairy cows
title_full Metabolomic biomarkers correlating with hepatic lipidosis in dairy cows
title_fullStr Metabolomic biomarkers correlating with hepatic lipidosis in dairy cows
title_full_unstemmed Metabolomic biomarkers correlating with hepatic lipidosis in dairy cows
title_short Metabolomic biomarkers correlating with hepatic lipidosis in dairy cows
title_sort metabolomic biomarkers correlating with hepatic lipidosis in dairy cows
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048253/
https://www.ncbi.nlm.nih.gov/pubmed/24888604
http://dx.doi.org/10.1186/1746-6148-10-122
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