Literature DB >> 23527872

Metabolic and endocrine profiles in sick neonatal foals are related to survival.

L Armengou1, E Jose-Cunilleras, J Ríos, C Cesarini, J Viu, L Monreal.   

Abstract

BACKGROUND: Sick neonatal foals suffer from a variety of endocrine and metabolic derangements that may be related to outcome. There are several hepatic and lipid metabolism blood markers that have never been assessed in neonatal foals.
OBJECTIVES: Assess panel of endocrine and metabolic variables in group of sick and healthy neonatal foals in order to describe their relationship with diagnosis and survival. ANIMALS: All neonatal foals referred to Unitat Equina-Fundació Hospital Clínic Veterinari during 3 consecutive foaling seasons and a group of healthy foals.
METHODS: Observational prospective study. Blood samples were obtained on admission and, when possible, after 24-48 h of hospitalization and immediately before discharge or death. Measured variables were triglycerides, nonsterified fatty acids, glucose, creatinine, urea, γ-glutamyltransferase, glutamate dehydrogenase (GLDH), insulin, cortisol, bile acids, and adrenocorticotropic hormone (ACTH). ACTH/cortisol and glucose/insulin ratios were calculated.
RESULTS: Urea, creatinine, and cortisol had median concentrations in septic and nonseptic foals 2- to 8-fold higher than in the control group (P < .001). Median ACTH concentration in the septic group was approximately 4 times higher than in nonseptic and control foals (P < .001). ACTH/cortisol ratio was significantly lower in sick foals compared to control foals (P < .001). A score was designed including creatinine, GLDH, and cortisol. When ≥ 2 of these variables were altered (P < .001), the foal had 32 times more risk of dying (OR, 31.7; 95% CI, 7.7-130.3). CONCLUSIONS AND CLINICAL IMPORTANCE: Plasma creatinine, GLDH, and cortisol should be determined in sick newborn foals on admission because of their association with survival.
Copyright © 2013 by the American College of Veterinary Internal Medicine.

Entities:  

Mesh:

Year:  2013        PMID: 23527872     DOI: 10.1111/jvim.12064

Source DB:  PubMed          Journal:  J Vet Intern Med        ISSN: 0891-6640            Impact factor:   3.333


  2 in total

1.  Glucocorticoid receptor density and binding affinity in healthy horses and horses with systemic inflammatory response syndrome.

Authors:  C J Hoffman; H C McKenzie; M O Furr; A Desrochers
Journal:  J Vet Intern Med       Date:  2015 Mar-Apr       Impact factor: 3.333

2.  Insulin dysregulation in horses with systemic inflammatory response syndrome.

Authors:  François-René Bertin; Debra Ruffin-Taylor; Allison Jean Stewart
Journal:  J Vet Intern Med       Date:  2018-05-10       Impact factor: 3.333

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.