Efficacy and Safety of Tirzepatide in Overweight and Obese Adult Patients with Type 1 Diabetes.

IF 5.7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Diabetes technology & therapeutics Pub Date : 2024-06-01 Epub Date: 2024-04-18 DOI:10.1089/dia.2024.0050
Satish K Garg, Halis K Akturk, Gurleen Kaur, Christie Beatson, Janet Snell-Bergeon
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Abstract

Introduction and Objective: Most patients with type 1 diabetes (T1D) in the United States are overweight (OW) or obese (OB), contributing to insulin resistance and suboptimal glucose control. The primary Food and Drug Administration-approved treatment for T1D is insulin, which may adversely affect weight. Tirzepatide is approved for managing type 2 diabetes, improves glucose control, facilitates weight loss, and improves cardiovascular disease outcomes. We assessed the use of tirzepatide in OW/OB subjects with T1D. Methods: This was a retrospective single-center real-world study in 62 OW/OB adult patients with T1D who were prescribed tirzepatide (treated group) and followed for 1 year. At least 3 months of use of tirzepatide was one of the inclusion criteria. Based on the inclusion criteria, this study represents 62 patients out of 184 prescribed tirzepatide. The control group included 37 OW/OB patients with T1D (computer frequency matched by age, duration of diabetes, gender, body mass index (BMI), and glucose control) who were not using any other weight-loss medications during the same period. The mean (±standard deviation [SD]) dose of weekly tirzepatide at 3 months was 5.6 ± 1.9 mg that increased to 9.7 ± 3.3 mg at 1 year. Results: The gender, mean baseline age, duration of diabetes, and glycosylated hemoglobin (HbA1c) were similar in the two groups, whereas BMI and weight were higher in the treated group. There were significantly larger declines in BMI and weight in the treated group than in controls across all time points among those in whom data were available. HbA1c decreased in the treated group as early as 3 months and was sustained through a 1-year follow-up (-0.67% at 1 year). As expected, insulin dose decreased at 3 months and throughout the study period. There were no reported hospitalizations from severe hypoglycemia or diabetic ketoacidosis. The mean glucose, time-in-range, time-above-range, SD, and coefficient of variation (continuous glucose monitoring metrics) significantly improved in the treated group. Conclusions: In this pilot (off label) study, we conclude that tirzepatide facilitated an average 18.5% weight loss (>46 pounds) and improved glucose control in OW/OB patients with T1D at 1 year. For safe use of tirzepatide in patients with T1D, we strongly recommend a large prospective randomized control trial in OW/OB patients with T1D.

Tirzepatide 对超重和肥胖的 1 型糖尿病成年患者的疗效和安全性。
导言和目标:美国大多数 1 型糖尿病(T1D)患者体重超重(OW)或肥胖(OB),导致胰岛素抵抗和血糖控制不理想。FDA 批准的治疗 T1D 的主要药物是胰岛素,而胰岛素可能会对体重产生不利影响。替扎帕肽获批用于控制 2 型糖尿病,可改善血糖控制、促进体重减轻并改善心血管疾病的预后。我们评估了在患有 T1D 的 OW/OB 受试者中使用替扎帕肽的情况:这是一项回顾性单中心真实世界研究,研究对象为 62 名 OW/OB 型 T1D 成年患者,他们均获处方替扎帕肽(治疗组),并随访一年。至少服用 3 个月的替哌肽是纳入标准之一。根据纳入标准,本研究代表了 184 名开具替扎帕肽处方的患者中的 62 名患者。对照组包括 37 名患有 T1D 的 OW/OB 患者(根据年龄、糖尿病病程、性别、体重指数和血糖控制情况进行计算机频率匹配),他们在同一时期未使用任何其他减肥药物。3个月时,每周服用替扎帕肽的平均剂量(±SD)为5.6±1.9毫克,一年后增至9.7±3.3毫克:两组患者的性别、平均基线年龄、糖尿病病程和 HbA1c 相似,而治疗组的 BMI 和体重更高。在有数据可查的人群中,治疗组在所有时间点的体重指数和体重降幅都明显大于对照组。治疗组的 HbA1c 早在 3 个月时就有所下降,并在一年的随访中保持不变(一年时为-0.67%)。正如预期的那样,胰岛素剂量在 3 个月和整个研究期间都有所下降。没有因严重低血糖或 DKA 而住院的报告。治疗组的平均血糖、TIR、TAR、SD 和 CV(CGM 指标)显著改善:在这项试验性(标签外)研究中,我们得出结论:替唑帕肽可使 OW/OB T1D 患者的体重平均减轻 18.5%(>46 磅),并在一年内改善血糖控制。为了在 T1D 患者中安全使用替扎帕肽,我们强烈建议在 T1D OW/OB 患者中开展大型前瞻性随机对照试验。
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来源期刊
Diabetes technology & therapeutics
Diabetes technology & therapeutics 医学-内分泌学与代谢
CiteScore
10.60
自引率
14.80%
发文量
145
审稿时长
3-8 weeks
期刊介绍: Diabetes Technology & Therapeutics is the only peer-reviewed journal providing healthcare professionals with information on new devices, drugs, drug delivery systems, and software for managing patients with diabetes. This leading international journal delivers practical information and comprehensive coverage of cutting-edge technologies and therapeutics in the field, and each issue highlights new pharmacological and device developments to optimize patient care.
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