Effect of dulaglutide injection on weight beyond glycemic control: Real-world observational study

A. Mohammed, S. Odhaib
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Abstract

Dulaglutide is an effective Glucagon-like Peptide-1 (GLP-1) Receptor Agonist (RA) in optimizing weight and glycemic control in obese patients with Type 2 Diabetes Mellitus (T2DM). The study's objective was the real-world evaluation of the metabolic effect of Dulaglutide on weight and glycemic control in patients with T2DM from Southern Iraq. This study is a six-month observational prospective longitudinal evaluation of 185 obese individuals with T2DM. They were initiated on Dulaglutide as an add-on drug with Oral Antidiabetic (OAD) or insulin therapy. General characteristics of the patients, glycated hemoglobin (HbA1c), blood glucose, lipid profile, and side effects profile were evaluated at the enrollment and the end of the study. The enrolled 185 obese patients with T2DM, had a T2DM duration (2 -14 years) and initial HbA1c range (6 - 19.5%), with different treatment modalities, including insulin, OADs, or both. The study showed a significant reduction in weight, HbA1c, and serum cholesterol, with minimal hypoglycemic events in 5% of patients (n=9). The gastrointestinal side effects were mild to moderate and self-limited in >96% of patients (n=178), while they were so severe in 4% (n=7) and caused discontinuation of Dulaglutide. Therefore, the insulin regimen was either stopped (n=28), changed (n=7), or reduced (n=9). No change on oral medications was performed in 141 patients. In conclusion, Dulaglutide 1.5 mg administered once a week significantly reduced the weight, HbA1c, Self-Monitoring of Blood Glucose (SMBG), and cholesterol levels with minimal hypoglycemic risk.
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杜拉鲁肽注射液对超出血糖控制的体重的影响:现实世界观察研究
Dulaglutide是一种有效的胰高血糖素样肽-1 (GLP-1)受体激动剂(RA),可优化肥胖2型糖尿病(T2DM)患者的体重和血糖控制。该研究的目的是评估杜拉鲁肽对伊拉克南部T2DM患者体重和血糖控制的代谢影响。本研究对185名肥胖T2DM患者进行了为期6个月的观察性前瞻性纵向评估。他们开始使用杜拉鲁肽作为口服抗糖尿病(OAD)或胰岛素治疗的附加药物。在入组时和研究结束时评估患者的一般特征、糖化血红蛋白(HbA1c)、血糖、血脂和副作用。纳入185例肥胖T2DM患者,T2DM病程(2 -14年)和初始HbA1c范围(6 - 19.5%),采用不同的治疗方式,包括胰岛素、OADs或两者兼而有之。研究显示,5%的患者体重、糖化血红蛋白(HbA1c)和血清胆固醇显著降低,低血糖事件发生率最低(n=9)。>96%的患者(n=178)的胃肠道副作用为轻至中度且自限性,而4%的患者(n=7)的胃肠道副作用严重,并导致杜拉鲁肽停药。因此,胰岛素治疗方案被停止(n=28)、改变(n=7)或减少(n=9)。141例患者口服药物没有变化。总之,每周给药1.5 mg杜拉鲁肽可显著降低体重、HbA1c、自我血糖监测(SMBG)和胆固醇水平,低血糖风险最小。
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