Miceli Diego D, García Jorge D, Pompili Gustavo A, Rey Amunategui Juan P, Ferraris Sergio, Pignataro Omar P, Guitelman Mirtha
Hospital School of Veterinary Medicine, University of Buenos Aires, Faculty of Veterinary Sciences, Buenos Aires, Argentina.
Veterinary Science Center, Maimonides University, Buenos Aires, Argentina.
J Feline Med Surg. 2022 Dec;24(12):1238-1244. doi: 10.1177/1098612X221074924. Epub 2022 Feb 8.
The aim of this study was to evaluate the safety and efficacy of cabergoline to control hypersomatotropism (HST) and diabetes mellitus (DM) in cats.
This was a prospective cohort study. Twenty-three cats with HST and concurrent DM were enrolled. Cats received a dose of 10 μg/kg cabergoline q48h PO for 6 months. Serum insulin-like growth factor 1 (IGF-1) and fructosamine concentrations, insulin dose and Insulin Resistance Index (IRI) were measured at the time of diagnosis of HST and at the start of cabergoline treatment (t0), and 3 months (t1) and 6 months (t2) during cabergoline treatment.
A decrease and normalization of serum IGF-1 concentration was observed in 35% and 26% of cats, respectively. Median IGF-1 (t0: 1350 ng/ml [range 832-1501]; t1: 1284 ng/ml [range 365-1501]; t2: 1240 ng/ml [range 263-1501]; = 0.016) decreased significantly. Twelve cats underwent diagnostic imaging of the pituitary area. The median pituitary height at t0 of cats that experienced an IGF-1 reduction (n = 5/12) was significantly lower compared with those that did not experience an IGF-1 reduction (n = 7/12) (3.2 mm [range 3.1-3.7] vs 6 mm [range 3.5-9.5]; = 0.011). Median fructosamine (t0: 628 µmol/l [range 400-963]; t1: 404 µmol/l [range 249-780]; t2: 400 µmol/l [range 260-815]; <0.0001), insulin dose (t0: 1.3 IU/kg [range 0.5-4.6]; t0: 0.5 IU/kg [range 0-2.3]; t2: 0.4 IU/kg [range 0-2.1]; <0.0001) and IRI (t0: 800 µmolIU/kgl [range 257-2700]; t1: 300 µmolIU/kgl [range 0-1498]; t2: 250 µmolIU/kgl [range 0-1498]; <0.0001) decreased significantly during cabergoline treatment. Eight cats achieved diabetic remission between months 1 and 6 of cabergoline treatment (median time to achieve remission: 3 months [range 1-6]). Three cats experienced asymptomatic hypoglycemia.
Cabergoline was effective in normalizing IGF-1 concentration in 26% of cats. Cabergoline improved diabetes control and was associated with remission of DM in 35% of cases. Cabergoline could be a treatment option for cats with HST and DM, especially in those cases with a relatively small pituitary tumor.
本研究旨在评估卡麦角林对控制猫的肢端肥大症(HST)和糖尿病(DM)的安全性和有效性。
这是一项前瞻性队列研究。纳入了23只患有肢端肥大症并发糖尿病的猫。猫口服卡麦角林,剂量为10μg/kg,每48小时一次,持续6个月。在肢端肥大症诊断时、卡麦角林治疗开始时(t0)以及卡麦角林治疗期间的3个月(t1)和6个月(t2)测量血清胰岛素样生长因子1(IGF-1)和果糖胺浓度、胰岛素剂量和胰岛素抵抗指数(IRI)。
分别在35%和26%的猫中观察到血清IGF-1浓度降低并恢复正常。IGF-1中位数(t0:1350ng/ml[范围832 - 1501];t1:1284ng/ml[范围365 - 1501];t2:1240ng/ml[范围263 - 1501];P = 0.016)显著降低。12只猫接受了垂体区域的诊断性成像。IGF-1降低的猫(n = 5/12)在t0时的垂体中位数高度显著低于未出现IGF-1降低的猫(n = 7/12)(3.2mm[范围3.1 - 3.7]对6mm[范围3.5 - 9.5];P = 0.011)。果糖胺中位数(t0:628μmol/l[范围400 - 963];t1:404μmol/l[范围249 - 780];t2:400μmol/l[范围260 - 815];P < 0.0001)、胰岛素剂量(t0:1.3IU/kg[范围0.5 - 4.6];t1:0.5IU/kg[范围0 - 2.3];t2:0.4IU/kg[范围0 - 2.1];P < 0.0001)和IRI(t0:800μmolIU/kgl[范围257 - 2700];t1:300μmolIU/kgl[范围0 - 1498];t2:250μmolIU/kgl[范围0 - 1498];P < 0.0001)在卡麦角林治疗期间显著降低。8只猫在卡麦角林治疗的第1至6个月实现糖尿病缓解(缓解的中位时间:3个月[范围1 - 6])。3只猫出现无症状性低血糖。
卡麦角林使26%的猫的IGF-1浓度恢复正常。卡麦角林改善了糖尿病控制,35%的病例实现了糖尿病缓解。卡麦角林可能是患有肢端肥大症和糖尿病猫的一种治疗选择,特别是在垂体肿瘤相对较小的病例中。