Romero-Vélez Félix, Rejas Juan, Ruiz de Gopegui Rafael
Hospital Clínic Veterinari, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain.
Department of Animal Medicine, Surgery and Anatomy, Universidad de León, 24071 León, Spain.
Animals (Basel). 2025 Aug 31;15(17):2561. doi: 10.3390/ani15172561.
While insulin is the standard of care for feline diabetes mellitus (FDM), non-insulin antidiabetic drugs (NIADs) are emerging as alternatives. This systematic review aims to synthesize and critically appraise the current evidence for the efficacy and safety of NIADs in cats.
A systematic review was conducted following PRISMA guidelines. Major databases were searched for studies evaluating NIADs in diabetic cats or at-risk/experimental models. Risk of bias was assessed using RoB 2 and ROBINS-I tools.
Twenty studies were included. In diabetic cats (10 studies), traditional agents (glipizide, metformin, acarbose) showed limited efficacy based on evidence with a high risk of bias. Newer SGLT2 inhibitors (bexagliflozin, velagliflozin) demonstrated high treatment success rates and non-inferiority to insulin but were associated with a significant risk of euglycemic diabetic ketoacidosis (eDKA). In at-risk/experimental models (10 studies), thiazolidinediones consistently improved insulin sensitivity, while glipizide was shown to accelerate islet amyloidosis.
The evidence supports a paradigm shift towards SGLT2 inhibitors as a viable oral monotherapy for select cases of FDM. This alters the clinical risk-benefit discussion from preventing hypoglycemia to mitigating eDKA. Significant evidence gaps remain, particularly the lack of high-quality RCTs and data in cats with common comorbidities.
虽然胰岛素是猫糖尿病(FDM)的标准治疗方法,但非胰岛素抗糖尿病药物(NIADs)正逐渐成为替代方案。本系统评价旨在综合并批判性地评估NIADs在猫身上的疗效和安全性的现有证据。
按照PRISMA指南进行系统评价。在主要数据库中检索评估NIADs在糖尿病猫或高危/实验模型中的研究。使用RoB 2和ROBINS-I工具评估偏倚风险。
纳入了20项研究。在糖尿病猫(10项研究)中,基于高偏倚风险的证据,传统药物(格列吡嗪、二甲双胍、阿卡波糖)显示出有限的疗效。新型钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂(贝西格列净、维格列净)显示出高治疗成功率且不劣于胰岛素,但与显著的正常血糖性糖尿病酮症酸中毒(eDKA)风险相关。在高危/实验模型(10项研究)中,噻唑烷二酮类药物持续改善胰岛素敏感性,而格列吡嗪显示会加速胰岛淀粉样变。
现有证据支持向SGLT2抑制剂转变,作为某些FDM病例可行的口服单一疗法。这改变了临床风险效益的讨论,从预防低血糖转变为减轻eDKA。仍存在显著的证据空白,特别是缺乏高质量的随机对照试验以及患有常见合并症的猫的数据。