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Metabolic changes induced by oral glucose tests in horses and their diagnostic use
BACKGROUND: Little is known about the implications of hyperinsulinemia on energy metabolism, and such knowledge might help understand the pathophysiology of insulin dysregulation. OBJECTIVES: Describe differences in the metabolic response to an oral glucose test, depending on the magnitude of the in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848347/ https://www.ncbi.nlm.nih.gov/pubmed/33277752 http://dx.doi.org/10.1111/jvim.15992 |
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author | Delarocque, Julien Frers, Florian Feige, Karsten Huber, Korinna Jung, Klaus Warnken, Tobias |
author_facet | Delarocque, Julien Frers, Florian Feige, Karsten Huber, Korinna Jung, Klaus Warnken, Tobias |
author_sort | Delarocque, Julien |
collection | PubMed |
description | BACKGROUND: Little is known about the implications of hyperinsulinemia on energy metabolism, and such knowledge might help understand the pathophysiology of insulin dysregulation. OBJECTIVES: Describe differences in the metabolic response to an oral glucose test, depending on the magnitude of the insulin response. ANIMALS: Twelve Icelandic horses in various metabolic states. METHODS: Horses were subjected to 3 oral glucose tests (OGT; 0.5 g/kg body weight glucose). Basal, 120 and 180 minutes samples were analyzed using a combined liquid chromatography tandem mass spectrometry and flow injection analysis tandem mass spectrometry metabolomic assay. Insulin concentrations were measured using an ELISA. Analysis was performed using linear models and partial least‐squares regression. RESULTS: The kynurenine : tryptophan ratio increased over time during the OGT (adjusted P‐value = .001). A high insulin response was associated with lower arginine (adjusted P‐value = .02) and carnitine (adjusted P‐value = .03) concentrations. A predictive model using only baseline samples performed well with as few as 7 distinct metabolites (sensitivity, 86%; 95% confidence interval [CI], 81%‐90%; specificity, 88%; 95% CI, 84%‐92%). CONCLUSIONS AND CLINICAL IMPORTANCE: Our results suggest induction of low‐grade inflammation during the OGT. Plasma arginine and carnitine concentrations were lower in horses with high insulin response and could constitute potential therapeutic targets. Development of screening tools to identify insulin‐dysregulated horses using only baseline blood sample appears promising. |
format | Online Article Text |
id | pubmed-7848347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78483472021-02-05 Metabolic changes induced by oral glucose tests in horses and their diagnostic use Delarocque, Julien Frers, Florian Feige, Karsten Huber, Korinna Jung, Klaus Warnken, Tobias J Vet Intern Med EQUINE BACKGROUND: Little is known about the implications of hyperinsulinemia on energy metabolism, and such knowledge might help understand the pathophysiology of insulin dysregulation. OBJECTIVES: Describe differences in the metabolic response to an oral glucose test, depending on the magnitude of the insulin response. ANIMALS: Twelve Icelandic horses in various metabolic states. METHODS: Horses were subjected to 3 oral glucose tests (OGT; 0.5 g/kg body weight glucose). Basal, 120 and 180 minutes samples were analyzed using a combined liquid chromatography tandem mass spectrometry and flow injection analysis tandem mass spectrometry metabolomic assay. Insulin concentrations were measured using an ELISA. Analysis was performed using linear models and partial least‐squares regression. RESULTS: The kynurenine : tryptophan ratio increased over time during the OGT (adjusted P‐value = .001). A high insulin response was associated with lower arginine (adjusted P‐value = .02) and carnitine (adjusted P‐value = .03) concentrations. A predictive model using only baseline samples performed well with as few as 7 distinct metabolites (sensitivity, 86%; 95% confidence interval [CI], 81%‐90%; specificity, 88%; 95% CI, 84%‐92%). CONCLUSIONS AND CLINICAL IMPORTANCE: Our results suggest induction of low‐grade inflammation during the OGT. Plasma arginine and carnitine concentrations were lower in horses with high insulin response and could constitute potential therapeutic targets. Development of screening tools to identify insulin‐dysregulated horses using only baseline blood sample appears promising. John Wiley & Sons, Inc. 2020-12-05 2021 /pmc/articles/PMC7848347/ /pubmed/33277752 http://dx.doi.org/10.1111/jvim.15992 Text en © 2020 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | EQUINE Delarocque, Julien Frers, Florian Feige, Karsten Huber, Korinna Jung, Klaus Warnken, Tobias Metabolic changes induced by oral glucose tests in horses and their diagnostic use |
title | Metabolic changes induced by oral glucose tests in horses and their diagnostic use |
title_full | Metabolic changes induced by oral glucose tests in horses and their diagnostic use |
title_fullStr | Metabolic changes induced by oral glucose tests in horses and their diagnostic use |
title_full_unstemmed | Metabolic changes induced by oral glucose tests in horses and their diagnostic use |
title_short | Metabolic changes induced by oral glucose tests in horses and their diagnostic use |
title_sort | metabolic changes induced by oral glucose tests in horses and their diagnostic use |
topic | EQUINE |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848347/ https://www.ncbi.nlm.nih.gov/pubmed/33277752 http://dx.doi.org/10.1111/jvim.15992 |
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