Comparison of methods to monitor dogs with hypercortisolism treated with trilostane.


Journal

Journal of veterinary internal medicine
ISSN: 1939-1676
Titre abrégé: J Vet Intern Med
Pays: United States
ID NLM: 8708660

Informations de publication

Date de publication:
Nov 2021
Historique:
revised: 09 09 2021
received: 30 01 2021
accepted: 10 09 2021
pubmed: 22 10 2021
medline: 24 12 2021
entrez: 21 10 2021
Statut: ppublish

Résumé

The use of adrenocorticotropic hormone stimulation test as method to monitor efficacy of trilostane treatment of hypercortisolism (HC) in dogs has been questioned. To evaluate and compare 12 methods with which to monitor efficacy of trilostane treatment in dogs with HC. Forty-five client-owned dogs with HC treated with trilostane q12h. Prospective cross-sectional observational study. The dogs were categorized as well-controlled, undercontrolled, and unwell through a clinical score obtained from an owner questionnaire. The ability to correctly identify trilostane-treatment control of dogs with HC with the following variables was evaluated: before trilostane serum cortisol (prepill), before-ACTH serum cortisol, post-ACTH serum cortisol, plasma endogenous ACTH concentrations, prepill/eACTH ratio, serum haptoglobin (Hp) concentration, serum alanine aminotransferase (ALT), gamma-glutamyl transferase (γGT) and alkaline phosphatase activity, urine specific gravity, and urinary cortisol : creatinine ratio. Ninety-four re-evaluations of 44 dogs were included; 5 re-evaluations of 5 unwell dogs were excluded. Haptoglobin was significantly associated with the clinical score (P < .001) and in the receiver operating characteristic analysis, Hp cutoff of 151 mg/dL correctly identified 90.0% of well-controlled dogs (specificity) and 65.6% of undercontrolled dogs (sensitivity). Alanine aminotransferase (P = .01) and γGT (P = .009) were significantly higher in undercontrolled dogs. Cutoff of ALT and γGT greater than or equal to 86 U/L and 5.8 U/L, respectively, were significantly associated with poor control of HC by trilostane. Of all the 12 variables, Hp, and to a lesser degree ALT and γGT, could be considered additional tools to the clinical picture to identify well-controlled and undercontrolled trilostane-treated dogs.

Sections du résumé

BACKGROUND BACKGROUND
The use of adrenocorticotropic hormone stimulation test as method to monitor efficacy of trilostane treatment of hypercortisolism (HC) in dogs has been questioned.
OBJECTIVES OBJECTIVE
To evaluate and compare 12 methods with which to monitor efficacy of trilostane treatment in dogs with HC.
ANIMALS METHODS
Forty-five client-owned dogs with HC treated with trilostane q12h.
METHODS METHODS
Prospective cross-sectional observational study. The dogs were categorized as well-controlled, undercontrolled, and unwell through a clinical score obtained from an owner questionnaire. The ability to correctly identify trilostane-treatment control of dogs with HC with the following variables was evaluated: before trilostane serum cortisol (prepill), before-ACTH serum cortisol, post-ACTH serum cortisol, plasma endogenous ACTH concentrations, prepill/eACTH ratio, serum haptoglobin (Hp) concentration, serum alanine aminotransferase (ALT), gamma-glutamyl transferase (γGT) and alkaline phosphatase activity, urine specific gravity, and urinary cortisol : creatinine ratio.
RESULTS RESULTS
Ninety-four re-evaluations of 44 dogs were included; 5 re-evaluations of 5 unwell dogs were excluded. Haptoglobin was significantly associated with the clinical score (P < .001) and in the receiver operating characteristic analysis, Hp cutoff of 151 mg/dL correctly identified 90.0% of well-controlled dogs (specificity) and 65.6% of undercontrolled dogs (sensitivity). Alanine aminotransferase (P = .01) and γGT (P = .009) were significantly higher in undercontrolled dogs. Cutoff of ALT and γGT greater than or equal to 86 U/L and 5.8 U/L, respectively, were significantly associated with poor control of HC by trilostane.
CONCLUSIONS AND CLINICAL IMPORTANCE CONCLUSIONS
Of all the 12 variables, Hp, and to a lesser degree ALT and γGT, could be considered additional tools to the clinical picture to identify well-controlled and undercontrolled trilostane-treated dogs.

Identifiants

pubmed: 34672018
doi: 10.1111/jvim.16269
pmc: PMC8692213
doi:

Substances chimiques

Enzyme Inhibitors 0
Dihydrotestosterone 08J2K08A3Y
trilostane L0FPV48Q5R
Hydrocortisone WI4X0X7BPJ

Types de publication

Journal Article Observational Study, Veterinary

Langues

eng

Sous-ensembles de citation

IM

Pagination

2616-2627

Subventions

Organisme : Dechra Products Ltd

Informations de copyright

© 2021 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine.

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Auteurs

Stefania Golinelli (S)

Department of Veterinary Medical Science, University of Bologna, Bologna, Italy.

Viviani de Marco (V)

Naya Especialidades, Sao Paulo, Brazil.

Rodolfo Oliveira Leal (RO)

CIISA - Centre for Interdisciplinary Research in Animal Health, Faculty of Veterinary Medicine, University of Lisbon, Lisbon, Portugal.

Andrea Barbarossa (A)

Department of Veterinary Medical Science, University of Bologna, Bologna, Italy.

Camilla Aniballi (C)

Department of Veterinary Medical Science, University of Bologna, Bologna, Italy.

Elisa Maietti (E)

Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.

Antonio Maria Tardo (AM)

Department of Veterinary Medical Science, University of Bologna, Bologna, Italy.

Sara Galac (S)

Department of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.

Federico Fracassi (F)

Department of Veterinary Medical Science, University of Bologna, Bologna, Italy.

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