Sokary Sara, Bawadi Hiba
Department of Human Nutrition, College of Health Science, QU-Health, Qatar University, Doha, Qatar.
Department of Human Nutrition, College of Health Science, QU-Health, Qatar University, Doha, Qatar.
Prim Care Diabetes. 2025 Jun;19(3):229-237. doi: 10.1016/j.pcd.2025.03.008. Epub 2025 Apr 11.
Obesity and type 2 diabetes mellites (T2DM) are intertwined epidemics that continue to pose significant challenges to global public health. We aim to review the available evidence on the metabolic effects of tirzepatide, focusing on weight loss and maintenance of lost weight, body composition alterations, appetite regulation, glycemic control, and lipid profile modulation. Tirzepatide administration for 72 weeks elicited significant weight reduction ranging from 5 % to 20.9 % across different trials in a dose-dependent manner. Furthermore, limited evidence showed that lost body weight may be primarily due to fat mass reduction. Tirzepatide also significantly decreased food intake, reduced overall appetite scores and increased fasting visual analog scale scores for satiety and fullness across different clinical trials. Moreover, tirzepatide exhibited favorable effects on glycemic control, with notable reductions in HbA1c levels ranging from 20.4 mmol/mol with the 5 mg dose to 28.2 mmol/mol with the 15 mg dose, following treatment durations lasting 40-52 weeks. Additionally, tirzepatide exerts a beneficial impact on lipid profile parameters, including reductions in total cholesterol, low-density lipoprotein cholesterol, and triglyceride levels, while increasing high-density lipoprotein cholesterol concentrations. Despite its efficacy, tirzepatide is associated with gastrointestinal adverse effects, which requires dose escalation strategies to enhance tolerability. Mild to moderate adverse events are commonly reported at higher doses, with discontinuation rates ranging from 4 % to 10 % across different dosages. In conclusion, tirzepatide has shown multifaceted metabolic effects, along with manageable adverse profiles, which makes it a promising therapeutic agent for addressing both obesity and T2DM. However, further long-term randomized controlled trials are warranted to reveal long-term efficacy and safety outcomes, particularly in diverse patient populations.
肥胖症与2型糖尿病(T2DM)是相互关联的流行病,继续对全球公共卫生构成重大挑战。我们旨在综述有关替尔泊肽代谢作用的现有证据,重点关注体重减轻及减轻后体重的维持、身体成分改变、食欲调节、血糖控制和血脂谱调节。在不同试验中,替尔泊肽给药72周可引起显著体重减轻,范围为5%至20.9%,呈剂量依赖性。此外,有限的证据表明,体重减轻可能主要归因于脂肪量减少。在不同临床试验中,替尔泊肽还显著减少食物摄入量、降低总体食欲评分并提高饱腹感和饱足感的空腹视觉模拟量表评分。此外,替尔泊肽对血糖控制具有良好效果,在持续40 - 52周的治疗后,糖化血红蛋白(HbA1c)水平显著降低,5 mg剂量时为20.4 mmol/mol,15 mg剂量时为28.2 mmol/mol。此外,替尔泊肽对血脂谱参数产生有益影响,包括总胆固醇、低密度脂蛋白胆固醇和甘油三酯水平降低,同时提高高密度脂蛋白胆固醇浓度。尽管替尔泊肽有效,但它与胃肠道不良反应相关,这需要采用剂量递增策略来提高耐受性。较高剂量时通常报告有轻度至中度不良事件,不同剂量的停药率范围为4%至10%。总之,替尔泊肽已显示出多方面的代谢作用,以及可控制的不良情况,这使其成为治疗肥胖症和T2DM的有前景的治疗药物。然而,有必要进行进一步的长期随机对照试验,以揭示长期疗效和安全性结果,特别是在不同患者群体中。