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Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment

CASE SUMMARY: An 8-year-old male neutered Persian cat was presented with polyuria, polydipsia, polyphagia and muscle weakness associated with a 7 month history of diabetes mellitus (DM). The cat had initially been treated with neutral protamine Hagedorn (NPH) insulin 2 U q12h, followed by porcine le...

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Autores principales: Muschner, Adriana Cunha, Varela, Fernanda Venzon, Hazuchova, Katarina, Niessen, Stijn JM, Pöppl, Álan Gomes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5912277/
https://www.ncbi.nlm.nih.gov/pubmed/29707227
http://dx.doi.org/10.1177/2055116918767708
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author Muschner, Adriana Cunha
Varela, Fernanda Venzon
Hazuchova, Katarina
Niessen, Stijn JM
Pöppl, Álan Gomes
author_facet Muschner, Adriana Cunha
Varela, Fernanda Venzon
Hazuchova, Katarina
Niessen, Stijn JM
Pöppl, Álan Gomes
author_sort Muschner, Adriana Cunha
collection PubMed
description CASE SUMMARY: An 8-year-old male neutered Persian cat was presented with polyuria, polydipsia, polyphagia and muscle weakness associated with a 7 month history of diabetes mellitus (DM). The cat had initially been treated with neutral protamine Hagedorn (NPH) insulin 2 U q12h, followed by porcine lente insulin 2 U q12h and, most recently, 3 U glargine insulin q12h, without improvement of clinical signs. The cat also suffered from concurrent symmetrical bilateral alopecia of thorax and forelimbs, abdominal distension and lethargy. Hyperadrenocorticism (HAC), specifically pituitary-dependent HAC, was suspected and confirmed through abdominal ultrasonography demonstrating bilateral adrenal enlargement, and a low-dose dexamethasone suppression test using 0.1 mg/kg dexamethasone intravenously. Trilostane treatment (initially 10 mg/cat PO q24h then increased to 10 mg/cat PO q12h) was started and insulin sensitivity gradually improved, ultimately leading to diabetic remission after an increased in trilostane dose to 13mg/cat PO q12h, 14 months after the DM diagnosis and 7 months after the initiation of trilostane therapy. RELEVANCE AND NOVEL INFORMATION: DM in cats with HAC is a difficult combination of diseases to treat. To our knowledge this is the first reported case of diabetic remission in a feline patient with HAC as a result of treatment with trilostane. Further work should focus on whether fine-tuning of trilostane-treatment protocols in cats with concurrent DM and HAC could lead to a higher proportion of diabetic remissions in this patient group.
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spelling pubmed-59122772018-04-27 Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment Muschner, Adriana Cunha Varela, Fernanda Venzon Hazuchova, Katarina Niessen, Stijn JM Pöppl, Álan Gomes JFMS Open Rep Case Report CASE SUMMARY: An 8-year-old male neutered Persian cat was presented with polyuria, polydipsia, polyphagia and muscle weakness associated with a 7 month history of diabetes mellitus (DM). The cat had initially been treated with neutral protamine Hagedorn (NPH) insulin 2 U q12h, followed by porcine lente insulin 2 U q12h and, most recently, 3 U glargine insulin q12h, without improvement of clinical signs. The cat also suffered from concurrent symmetrical bilateral alopecia of thorax and forelimbs, abdominal distension and lethargy. Hyperadrenocorticism (HAC), specifically pituitary-dependent HAC, was suspected and confirmed through abdominal ultrasonography demonstrating bilateral adrenal enlargement, and a low-dose dexamethasone suppression test using 0.1 mg/kg dexamethasone intravenously. Trilostane treatment (initially 10 mg/cat PO q24h then increased to 10 mg/cat PO q12h) was started and insulin sensitivity gradually improved, ultimately leading to diabetic remission after an increased in trilostane dose to 13mg/cat PO q12h, 14 months after the DM diagnosis and 7 months after the initiation of trilostane therapy. RELEVANCE AND NOVEL INFORMATION: DM in cats with HAC is a difficult combination of diseases to treat. To our knowledge this is the first reported case of diabetic remission in a feline patient with HAC as a result of treatment with trilostane. Further work should focus on whether fine-tuning of trilostane-treatment protocols in cats with concurrent DM and HAC could lead to a higher proportion of diabetic remissions in this patient group. SAGE Publications 2018-04-16 /pmc/articles/PMC5912277/ /pubmed/29707227 http://dx.doi.org/10.1177/2055116918767708 Text en © The Author(s) 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Muschner, Adriana Cunha
Varela, Fernanda Venzon
Hazuchova, Katarina
Niessen, Stijn JM
Pöppl, Álan Gomes
Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment
title Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment
title_full Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment
title_fullStr Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment
title_full_unstemmed Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment
title_short Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment
title_sort diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5912277/
https://www.ncbi.nlm.nih.gov/pubmed/29707227
http://dx.doi.org/10.1177/2055116918767708
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