Ciclosporin therapy is associated with minimal changes in calcium metabolism in dogs with atopic dermatitis

Marcel Kovalik, Richard J. Mellanby, Helen Evans, Jacqueline Berry, Adrianus Van Den Broek, Keith L. Thoday

Research output: Contribution to journalArticlepeer-review

Abstract

Background Ciclosporin is widely used in the management of canine atopic dermatitis. In humans, ciclosporin therapy has been linked to disturbances in calcium metabolism and resultant skeletal disorders.

Objectives The objective of this study was to assess calcium homeostasis in dogs before and after a 6 week course of once daily oral ciclosporin at the licensed dose (5 mg/kg).

Animals Sixteen client-owned dogs with spontaneous atopic dermatitis.

Methods Serum concentrations of calcium, phosphate, creatinine, 25-hydroxyvitamin D, 1,25-dihyroxyvitamin D and plasma concentrations of ionized calcium and parathyroid hormone (PTH) were measured, together with the urinary fractional excretion of calcium and phosphate. The extent of skin lesions was scored using the Canine Atopic Dermatitis Extent and Severity Index (CADESI)-03 and the degree of pruritus by the Edinburgh Pruritus Scale prior to and at the end of the study.

Results The CADESI-03 and the Edinburgh Pruritus Scale scores decreased satisfactorily in all dogs by the end of the study. Plasma PTH concentrations were significantly increased (P = 0.02) following ciclosporin treatment, whereas all other biochemical parameters were not significantly different from their starting values. The increase in PTH was mild in most cases and the proportion of dogs that had a PTH concentration above the reference range was not significantly different following treatment.

Conclusions and clinical importance This study indicates that ciclosporin has minimal impact on calcium metabolism in dogs with atopic dermatitis when used at the licensed and clinically effective dosage for 6 weeks.

Original languageEnglish
Pages (from-to)-
Number of pages7
JournalVeterinary Dermatology
Volume23
Issue number6
DOIs
Publication statusPublished - Dec 2012

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