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The efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies

BACKGROUND: A previous six-week (wk) study demonstrated the potential of the sodium-glucose linked transport inhibitor velagliflozin as a novel treatment for equine insulin dysregulation. The present study examined the safety and efficacy of velagliflozin over 16 wk. of treatment, and over 4 wk. of...

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Autores principales: Meier, A., de Laat, M., Reiche, D., Fitzgerald, D., Sillence, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390376/
https://www.ncbi.nlm.nih.gov/pubmed/30808423
http://dx.doi.org/10.1186/s12917-019-1811-2
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author Meier, A.
de Laat, M.
Reiche, D.
Fitzgerald, D.
Sillence, M.
author_facet Meier, A.
de Laat, M.
Reiche, D.
Fitzgerald, D.
Sillence, M.
author_sort Meier, A.
collection PubMed
description BACKGROUND: A previous six-week (wk) study demonstrated the potential of the sodium-glucose linked transport inhibitor velagliflozin as a novel treatment for equine insulin dysregulation. The present study examined the safety and efficacy of velagliflozin over 16 wk. of treatment, and over 4 wk. of withdrawal. Twenty-four insulin dysregulated ponies were selected, based on their hyper-responsiveness to a diet challenge meal containing 3.8 g non-structural carbohydrates (NSC)/kg bodyweight (BW). Ponies with serum insulin > 90 μIU/mL either 2 or 4 h after feeding were enrolled, and randomly allocated to receive either velagliflozin (0.3 mg/kg BW orally once daily, n = 12), or a placebo (n = 10–12) for 16 wk. The subjects were fed 7.5 g NSC/kg BW/day to maintain a fat body condition. Safety was assessed through daily monitoring, veterinary examination, and the measurement of fasting blood glucose, biochemistry and haematology. Efficacy at reducing post-prandial hyperinsulinemia was assessed using a diet challenge every 8 wk. during treatment and 4 wk. after withdrawal. RESULTS: Velagliflozin was well accepted by all subjects and caused no adverse effects or hypoglycaemia. Post-prandial serum insulin (insulin C(max)) did not change significantly in the control animals over the entire study period (P = 0.101). In contrast, insulin C(max) (mean ± SE) concentrations fell over time in the velagliflozin-treated group from 205 ± 25 μIU/mL in wk. 0, to 119 ± 19 μIU/mL (P = 0.015) and 117 ± 15 μIU/ml (P = 0.029) after 8 and 16 wk. of treatment, respectively. Although the insulin C(max) in this group was not significantly lower than in controls at wk-8 (P = 0.061), it was lower at wk-16 (P = 0.003), and all 12 treated ponies were below the previously-determined risk threshold for laminitis at this time. After 4 wk. withdrawal, the insulin C(max) returned to 199 ± 36 μIU/mL in the treated group, with no rebound effect. CONCLUSIONS: Velagliflozin appears to be a promising and safe treatment for equine insulin dysregulation, bringing post-prandial insulin concentrations below the laminitis risk threshold, albeit without normalising them. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-019-1811-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-63903762019-03-28 The efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies Meier, A. de Laat, M. Reiche, D. Fitzgerald, D. Sillence, M. BMC Vet Res Research Article BACKGROUND: A previous six-week (wk) study demonstrated the potential of the sodium-glucose linked transport inhibitor velagliflozin as a novel treatment for equine insulin dysregulation. The present study examined the safety and efficacy of velagliflozin over 16 wk. of treatment, and over 4 wk. of withdrawal. Twenty-four insulin dysregulated ponies were selected, based on their hyper-responsiveness to a diet challenge meal containing 3.8 g non-structural carbohydrates (NSC)/kg bodyweight (BW). Ponies with serum insulin > 90 μIU/mL either 2 or 4 h after feeding were enrolled, and randomly allocated to receive either velagliflozin (0.3 mg/kg BW orally once daily, n = 12), or a placebo (n = 10–12) for 16 wk. The subjects were fed 7.5 g NSC/kg BW/day to maintain a fat body condition. Safety was assessed through daily monitoring, veterinary examination, and the measurement of fasting blood glucose, biochemistry and haematology. Efficacy at reducing post-prandial hyperinsulinemia was assessed using a diet challenge every 8 wk. during treatment and 4 wk. after withdrawal. RESULTS: Velagliflozin was well accepted by all subjects and caused no adverse effects or hypoglycaemia. Post-prandial serum insulin (insulin C(max)) did not change significantly in the control animals over the entire study period (P = 0.101). In contrast, insulin C(max) (mean ± SE) concentrations fell over time in the velagliflozin-treated group from 205 ± 25 μIU/mL in wk. 0, to 119 ± 19 μIU/mL (P = 0.015) and 117 ± 15 μIU/ml (P = 0.029) after 8 and 16 wk. of treatment, respectively. Although the insulin C(max) in this group was not significantly lower than in controls at wk-8 (P = 0.061), it was lower at wk-16 (P = 0.003), and all 12 treated ponies were below the previously-determined risk threshold for laminitis at this time. After 4 wk. withdrawal, the insulin C(max) returned to 199 ± 36 μIU/mL in the treated group, with no rebound effect. CONCLUSIONS: Velagliflozin appears to be a promising and safe treatment for equine insulin dysregulation, bringing post-prandial insulin concentrations below the laminitis risk threshold, albeit without normalising them. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-019-1811-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-26 /pmc/articles/PMC6390376/ /pubmed/30808423 http://dx.doi.org/10.1186/s12917-019-1811-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Meier, A.
de Laat, M.
Reiche, D.
Fitzgerald, D.
Sillence, M.
The efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies
title The efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies
title_full The efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies
title_fullStr The efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies
title_full_unstemmed The efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies
title_short The efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies
title_sort efficacy and safety of velagliflozin over 16 weeks as a treatment for insulin dysregulation in ponies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390376/
https://www.ncbi.nlm.nih.gov/pubmed/30808423
http://dx.doi.org/10.1186/s12917-019-1811-2
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