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September 9, 2024 at 10:06 am #21943Robert Oglesby DVMKeymaster
Considering the recent move to transporting horses to the equine clinic for routine work, this is an important finding. Transport of non-insulin-dysregulated horses will raise their tested insulin levels above the diagnostic threshold for insulin dysregulation.
DrOThe impact of short-term transportation stress on insulin and oral sugar responses in insulin dysregulated and non-insulin dysregulated horses
Equine Vet J. 2024 Sep 4. doi: 10.1111/evj.14403. Online ahead of print.
Authors
Erica T Jacquay 1 , Patricia A Harris 2 , Amanda A Adams 1
Affiliations1 M. H. Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, Kentucky, USA.
2 Equine Studies Group, Waltham Petcare Science Institute, Waltham on the Wolds, Leicestershire, UK.PMID: 39233387
DOI: 10.1111/evj.14403Abstract
in English, PortugueseBackground: It is unknown whether short-term transportation affects endocrine responses similarly in horses with and without insulin dysregulation (ID).
Objectives: To characterise the effect of short-term transportation on stress parameters and insulin responses to an oral sugar test (OST) in horses with and without ID.
Study design: Longitudinal cohort study.
Methods: Fourteen adult non-pregnant, non-PPID mares of mixed light breeds were grouped as either ID (n = 7) or non-ID (n = 7) based on endocrine testing. Over 2 weeks, horses were transported once, in groups of 3-4 in a horse trailer on a round-trip journey of ~1.5 h. Blood and saliva were collected 24 h and 1 h pre-transportation, directly after unloading and 15 min, 1 h, 3 h plus 24 h post-transportation. An OST was performed 24 h pre-transportation and 3 h post-transportation with a pre- (T0) and post-OST sample collected 60 min later (T60). Heart rates and rectal temperatures were also collected throughout the study. Serum insulin, serum cortisol, and plasma glucose were measured using validated assays. Repeated measures ANOVA were used to determine differences after transportation and between ID and non-ID horses. Non-normal data were log-transformed and multiple comparisons were adjusted using Bonferroni post hoc tests.
Results: Mean insulin was higher in ID horses versus non-ID horses (mean = 109.9 μU/mL vs. 30.2 μU/mL, p < 0.001; 95% CI for mean difference = [55.6-107.7 μU/mL]). Mean serum insulin increased following OST at T60 in ID horses pre- (154.6 μU/mL, p = 0.04; 95% CI = [86.3-223.0 μU/mL]) and post-transportation (284.6 μU/mL, p = 0.03; 95% CI = [114.3-454.8 μU/mL]). Non-ID horses had a mean OST T60 insulin post-transportation of 56.6 μU/mL (95% CI = [29.1-84.1 μU/mL]); above recognised threshold [45 μU/mL] for ID diagnosis. Main limitations: Small number of horses, only mares used, and OST not performed immediately post-transportation. Conclusions: Performing an OST 3 h following short-term transportation may result in inaccurate ID status.
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