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Insulin dysregulation in horses with systemic inflammatory response syndrome

BACKGROUND: Systemic inflammation is a cause of insulin dysregulation in many species, but the insulin and glucose dynamics in adult horses diagnosed with systemic inflammatory response syndrome (SIRS) are poorly documented. HYPOTHESIS/OBJECTIVES: In SIRS in horses, insulin and glucose dynamics will...

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Autores principales: Bertin, François‐René, Ruffin‐Taylor, Debra, Stewart, Allison Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060318/
https://www.ncbi.nlm.nih.gov/pubmed/29749643
http://dx.doi.org/10.1111/jvim.15138
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author Bertin, François‐René
Ruffin‐Taylor, Debra
Stewart, Allison Jean
author_facet Bertin, François‐René
Ruffin‐Taylor, Debra
Stewart, Allison Jean
author_sort Bertin, François‐René
collection PubMed
description BACKGROUND: Systemic inflammation is a cause of insulin dysregulation in many species, but the insulin and glucose dynamics in adult horses diagnosed with systemic inflammatory response syndrome (SIRS) are poorly documented. HYPOTHESIS/OBJECTIVES: In SIRS in horses, insulin and glucose dynamics will be altered and associated with survival. ANIMALS: Adult horses diagnosed with SIRS admitted to a referral hospital. METHODS: Prospective study enrolling horses diagnosed with SIRS in which serum insulin and glucose concentrations were measured. Horses were grouped by outcome (survival, hyperinsulinemia, and hyperglycemia) and compared with P < .05 considered significant. RESULTS: Fifty‐eight horses were included in the study and 36 (62%) survived. At admission, 21 horses (36%) were hyperinsulinemic and 44 horses (88%) were hyperglycemic, with survivors having significantly higher serum insulin and a significantly lower serum glucose concentration. Horses diagnosed with hyperinsulinemia at any time during hospitalization were 4 times more likely to survive whereas horses that were hyperglycemic at any time during hospitalization were 5 times less likely to survive. Serum glucose concentration and presence of hyperglycemia both were associated with severity of disease. Insulin/glucose ratio, reflecting insulin secretion, was significantly higher in survivors whereas glucose/insulin ratio, reflecting peripheral tissue insulin resistance, was significantly lower in nonsurvivors. Only in survivors was there a significant correlation between serum insulin and glucose concentrations. CONCLUSIONS AND CLINICAL IMPORTANCE: Hyperinsulinemia and hyperglycemia are common features of SIRS in horses, but those presenting with relative hypoinsulinemia and corresponding hyperglycemia suggestive of endocrine pancreatic dysfunction have a worse prognosis.
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spelling pubmed-60603182018-07-31 Insulin dysregulation in horses with systemic inflammatory response syndrome Bertin, François‐René Ruffin‐Taylor, Debra Stewart, Allison Jean J Vet Intern Med EQUID BACKGROUND: Systemic inflammation is a cause of insulin dysregulation in many species, but the insulin and glucose dynamics in adult horses diagnosed with systemic inflammatory response syndrome (SIRS) are poorly documented. HYPOTHESIS/OBJECTIVES: In SIRS in horses, insulin and glucose dynamics will be altered and associated with survival. ANIMALS: Adult horses diagnosed with SIRS admitted to a referral hospital. METHODS: Prospective study enrolling horses diagnosed with SIRS in which serum insulin and glucose concentrations were measured. Horses were grouped by outcome (survival, hyperinsulinemia, and hyperglycemia) and compared with P < .05 considered significant. RESULTS: Fifty‐eight horses were included in the study and 36 (62%) survived. At admission, 21 horses (36%) were hyperinsulinemic and 44 horses (88%) were hyperglycemic, with survivors having significantly higher serum insulin and a significantly lower serum glucose concentration. Horses diagnosed with hyperinsulinemia at any time during hospitalization were 4 times more likely to survive whereas horses that were hyperglycemic at any time during hospitalization were 5 times less likely to survive. Serum glucose concentration and presence of hyperglycemia both were associated with severity of disease. Insulin/glucose ratio, reflecting insulin secretion, was significantly higher in survivors whereas glucose/insulin ratio, reflecting peripheral tissue insulin resistance, was significantly lower in nonsurvivors. Only in survivors was there a significant correlation between serum insulin and glucose concentrations. CONCLUSIONS AND CLINICAL IMPORTANCE: Hyperinsulinemia and hyperglycemia are common features of SIRS in horses, but those presenting with relative hypoinsulinemia and corresponding hyperglycemia suggestive of endocrine pancreatic dysfunction have a worse prognosis. John Wiley and Sons Inc. 2018-05-10 2018 /pmc/articles/PMC6060318/ /pubmed/29749643 http://dx.doi.org/10.1111/jvim.15138 Text en Copyright © 2018 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. 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 EQUID
Bertin, François‐René
Ruffin‐Taylor, Debra
Stewart, Allison Jean
Insulin dysregulation in horses with systemic inflammatory response syndrome
title Insulin dysregulation in horses with systemic inflammatory response syndrome
title_full Insulin dysregulation in horses with systemic inflammatory response syndrome
title_fullStr Insulin dysregulation in horses with systemic inflammatory response syndrome
title_full_unstemmed Insulin dysregulation in horses with systemic inflammatory response syndrome
title_short Insulin dysregulation in horses with systemic inflammatory response syndrome
title_sort insulin dysregulation in horses with systemic inflammatory response syndrome
topic EQUID
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060318/
https://www.ncbi.nlm.nih.gov/pubmed/29749643
http://dx.doi.org/10.1111/jvim.15138
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