Rivera Gutierrez Rene, Tama Elif, Bechenati Dima, Castañeda Hernandez Regina, Bennett Pamela K, McNally Allyson W, Fansa Sima, Anazco Diego, Acosta Andres, Hurtado Andrade Maria D
Division of Endocrinology, Diabetes, and Metabolism, Mayo Clinic, Jacksonville, FL, USA; Precision Medicine for Obesity Program, Mayo Clinic, Rochester, MN, USA.
Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN, USA.
Mayo Clin Proc. 2025 Feb;100(2):265-275. doi: 10.1016/j.mayocp.2024.07.006. Epub 2024 Nov 26.
To determine the effect of tirzepatide on weight, diabetes control, and insulin requirements, and its safety profile in adults with type 1 diabetes (T1D) and overweight or obesity.
This is a retrospective study of adults with T1D using tirzepatide for overweight/obesity treatment between June 1, 2022, and October 31, 2023, at Mayo Clinic. Fifty-one patients fulfilled inclusion and exclusion criteria (adults with established T1D diagnosis and a body mass index ≥27 kg/m using tirzepatide for 3 months or longer and without a history of bariatric surgery or active malignancy). Data were collected from the electronic medical record and reported as median (Q1-Q3).
Most individuals were female (30, 58.8%), White (49, 96.1%), and with obesity class III (21, 41.2%). During a median follow-up time of 8.0 (Q1-Q3: 4.0-10.0) months, the total body weight loss was 8.5% (Q1-Q3: 5.3%-13.8%) (P<.01). At 12 months, total body weight loss was 12.2% (Q1-Q3: 7.3%-19.8%) (n=26). By the last follow-up, hemoglobin A decreased by 0.9% (Q1-Q3: 0.3%-1.1%) (P<.0001) and daily insulin requirements by 31.6% (Q1-Q3: -48.0% to -10.9% (P<.01). Basal and bolus insulin doses decreased proportionally, with a more precipitous decline during the first 6 months of tirzepatide therapy. The use of tirzepatide was associated with an improvement of cardiometabolic parameters. There was no increased incidence of hypoglycemia. The most common side effect was nausea (7, 13.7%).
Tirzepatide for the treatment of overweight and obesity in adults with T1D leads to substantial weight loss, improved diabetes control, and decreased insulin requirements, without worsening hypoglycemia. Future studies are needed to ascertain the long-term effect of tirzepatide in this population, ideally focusing on cardiovascular outcomes.
确定替尔泊肽对1型糖尿病(T1D)合并超重或肥胖成人的体重、糖尿病控制情况及胰岛素需求量的影响,及其安全性。
这是一项对2022年6月1日至2023年10月31日期间在梅奥诊所使用替尔泊肽治疗超重/肥胖的T1D成人患者的回顾性研究。51名患者符合纳入和排除标准(确诊为T1D的成人,体重指数≥27kg/m²,使用替尔泊肽3个月或更长时间,且无减重手术史或活动性恶性肿瘤病史)。数据从电子病历中收集,并以中位数(第一四分位数-第三四分位数)报告。
大多数患者为女性(30例,58.8%),白人(49例,96.1%),且为III级肥胖(21例,41.2%)。在中位随访时间8.0(第一四分位数-第三四分位数:4.0-10.0)个月期间,总体重减轻了8.5%(第一四分位数-第三四分位数:5.3%-13.8%)(P<0.01)。在12个月时,总体重减轻了12.2%(第一四分位数-第三四分位数:7.3%-19.8%)(n=26)。到最后一次随访时,糖化血红蛋白下降了0.9%(第一四分位数-第三四分位数:0.3%-1.1%)(P<0.0001),每日胰岛素需求量下降了31.6%(第一四分位数-第三四分位数:-48.0%至-10.9%)(P<0.01)。基础胰岛素和餐时胰岛素剂量成比例下降,在替尔泊肽治疗的前6个月下降更为明显。使用替尔泊肽与心脏代谢参数的改善相关。低血糖发生率没有增加。最常见的副作用是恶心(7例,13.7%)。
替尔泊肽用于治疗T1D合并超重和肥胖的成人可导致显著体重减轻、改善糖尿病控制并降低胰岛素需求量,且不会使低血糖情况恶化。需要进一步的研究来确定替尔泊肽在该人群中的长期效果,理想情况下应关注心血管结局。