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Peer-reviewed veterinary case report

Hypothyroidism with acromegaly and diabetes in a Samoyed dog

By Johnstone, T et al.·Published in Australian veterinary journal·2014·University of Melbourne Veterinary Hospital, Australia·View original on PubMed

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Original publication title: Hypothyroidism associated with acromegaly and insulin-resistant diabetes mellitus in a Samoyed.

Species:
dog

Plain-English summary

A 4-year-old male Samoyed was brought in for shifting lameness, exercise intolerance, and excessive thirst, which had been ongoing for several months. Despite treatments like zinc supplements and antibiotics, his symptoms persisted. Tests revealed he had hypothyroidism and diabetes, along with insulin resistance and excess growth hormone. After starting treatment for hypothyroidism, the dog's diabetes improved, suggesting that managing the thyroid condition can help with insulin resistance.

People also search for: Samoyed diabetes treatment · dog hypothyroidism symptoms · insulin resistance in dogs · dog shifting lameness causes

Abstract

BACKGROUND: The aetiology of insulin resistance (IR) in naturally occurring canine hypothyroidism is poorly understood and likely multifactorial. Excess secretion of growth hormone (GH) by transdifferentiated pituitary cells may contribute to IR in some hypothyroid dogs, but although this has been demonstrated in experimental studies, it has not yet been documented in clinical cases. CASE REPORT: A 4-year-old male entire Samoyed presented with an 8-month history of pedal hyperkeratosis and shifting lameness, which had been unresponsive to zinc supplementation, antibiotics and glucocorticoid therapy. The dog also exhibited exercise intolerance and polydipsia of 12 and 2 months duration, respectively. On physical examination, obesity, poor coat condition, widened interdental spaces and mild respiratory stridor were noted. Initial laboratory test results revealed concurrent hypothyroidism and diabetes mellitus (DM). Further investigations showed IR, GH excess and a paradoxical increase of GH following stimulation with thyrotropin-releasing hormone. CONCLUSIONS: To the authors' knowledge, this is the first reported case that suggests that GH alterations may have clinical significance in naturally occurring hypothyroidism. Among other factors, hypothyroidism-induced GH excess should be considered as a possible cause of IR in patients suffering from hypothyroidism and concurrent DM. In such cases, DM may reverse with treatment of hypothyroidism, as was documented in this case.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/25290378/