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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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. |
format | Online Article Text |
id | pubmed-6390376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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