Insulin glargine 300 U/ml for the treatment of feline diabetes mellitus

Author:

Linari Guido1,Fleeman Linda2,Gilor Chen3,Giacomelli Lucia1,Fracassi Federico1ORCID

Affiliation:

1. Department of Veterinary Medical Sciences, University of Bologna, Bologna, Italy

2. Animal Diabetes Australia, Mulgrave, VIC, Australia

3. College of Veterinary Medicine, University of Florida, Gainesville, FL, USA

Abstract

Objectives The study aimed to evaluate the efficacy and safety of insulin glargine 300 U/ml (IGla-U300) in cats with variable duration of diabetes mellitus (DM). Methods Thirteen client-owned cats with DM completed a prospective clinical trial. Four cats were highly suspected of hypersomatotropism and excluded from the insulin efficacy evaluation. All cats were treated with IGla-U300 SC at a starting dosage of 0.5 U/kg q12h and fed with a low carbohydrate diet. Cats were monitored for 8 weeks with a once-weekly at-home 16 h blood glucose curve (BGC) and a questionnaire evaluating the presence of DM-related clinical signs. In-clinic evaluations, including serum fructosamine measurement, were scheduled within 3 days of the first, third, sixth and eighth BGC. Glycemic variability was assessed by calculating the SD of each BGC. Results Excluding four cats suspected of hypersomatotropism, at the time of the eighth BGC, improved or absent polyuria, polydipsia, polyphagia, weight loss, lethargy and improved or normal general demeanor were reported in 8/9 (88%), 8/9 (88%), 7/9 (77%), 7/9 (77%), 7/9 (77%) and 8/9 (88%) cats, respectively. Two cats achieved remission after 29 and 53 days. Another two cats went into remission after the end of the study (days 82 and 96). All cats that achieved remission were newly diagnosed diabetics. Median (range) serum fructosamine concentration significantly decreased when comparing the time of enrollment (604 [457–683] µmol/l) with the eighth week of treatment (366 [220–738] µmol/l) ( P = 0.02). In all 13 cats, biochemical hypoglycemia (blood glucose <60 mg/dl; <3.3 mmol/l) was detected in 13/104 (12.5%) BGCs, while clinical signs suggesting hypoglycemic episodes were not reported. Glycemic variability was significantly lower at the fifth BGC when comparing cats that achieved remission with cats that did not achieve remission ( P = 0.02). Conclusions and relevance IGla-U300 seems effective and safe for the treatment of feline diabetes, but more long- term and comparative clinical trials are needed.

Publisher

SAGE Publications

Subject

Small Animals

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Continuous Glucose Monitoring in Dogs and Cats;Veterinary Clinics of North America: Small Animal Practice;2023-05

2. Insulin Therapy in Small Animals, Part 2: Cats;Veterinary Clinics of North America: Small Animal Practice;2023-05

3. Safety and effectiveness of the sodium‐glucose cotransporter inhibitor bexagliflozin in cats newly diagnosed with diabetes mellitus;Journal of Veterinary Internal Medicine;2023-05

4. Monitoring of Diabetes Mellitus Using the Flash Glucose Monitoring System: The Owners’ Point of View;Veterinary Sciences;2023-03-07

5. Traitement du diabète sucré : choisir l’insuline la plus adaptée (type, dose, fréquence);Le Nouveau Praticien Vétérinaire canine & féline;2023

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