SGLT2 inhibitor use in the management of feline diabetes mellitus.

IF 1.5 4区 农林科学 Q3 PHARMACOLOGY & PHARMACY Journal of veterinary pharmacology and therapeutics Pub Date : 2024-07-02 DOI:10.1111/jvp.13466
Audrey K Cook, Ellen Behrend
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Abstract

Sodium-glucose cotransporter-2 (SGLT2) inhibitors are routinely used in the management of human type 2 diabetes and have been shown to effectively mitigate hyperglycemia and reduce the risks of cardiovascular and renal compromise. Two SGLT2 inhibitors, namely bexagliflozin and velagliflozin, were recently FDA approved for the treatment of uncomplicated feline diabetes mellitus. These oral hypoglycemic agents are a suitable option for many newly diagnosed cats, with rapid improvements in glycemic control and clinical signs. Suitable candidates must have some residual β-cell function, as some endogenous insulin production is required to prevent ketosis. Appropriate patient selection and monitoring are necessary, and practitioners should be aware of serious complications such as euglycemic diabetic ketoacidosis.

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在猫科动物糖尿病治疗中使用 SGLT2 抑制剂。
钠-葡萄糖共转运体-2(SGLT2)抑制剂是治疗人类 2 型糖尿病的常规药物,已被证明能有效缓解高血糖症状,降低心血管和肾脏受损的风险。最近,美国食品及药物管理局批准了两种 SGLT2 抑制剂(即 bexagliflozin 和 velagliflozin)用于治疗无并发症的猫科动物糖尿病。这些口服降糖药是许多新确诊猫咪的合适选择,可迅速改善血糖控制和临床症状。合适的患者必须有一些残余的β细胞功能,因为需要一些内源性胰岛素分泌来防止酮症。有必要对患者进行适当的选择和监测,从业人员应注意优生糖尿病酮症酸中毒等严重并发症。
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来源期刊
CiteScore
3.10
自引率
15.40%
发文量
69
审稿时长
8-16 weeks
期刊介绍: The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.
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