Liu Ligang, Shi Hekai, Xie Merilyn, Sun Yuxiao, Nahata Milap C
Institute of Therapeutic Innovations and Outcomes (ITIO), College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.
Department of Bariatric and Metabolic Surgery, Fudan University Affiliated Huadong Hospital, Shanghai 200040, China.
Pharmaceuticals (Basel). 2025 Apr 30;18(5):668. doi: 10.3390/ph18050668.
Obesity and type 2 diabetes (T2D) are major public health concerns. Tirzepatide has shown promise in recent clinical trials. This systematic review and meta-analysis aim to evaluate the efficacy and safety of tirzepatide in adults with obesity or type 2 diabetes, compared to placebo, GLP-1 receptor agonists (GLP-1 RAs), and insulin. : PubMed, Embase, and the Cochrane Library were searched on 17 January 2024, focusing on phase II and III randomized controlled trials (RCTs). We included studies involving adults with T2D or obesity, comparing tirzepatide to placebo, GLP-1 RAs, or insulin. The primary outcomes were the proportion of participants achieving ≥5%, ≥10%, and ≥15% weight loss targets. Secondary outcomes included changes in body weight, waist circumference, HbA1c levels, and blood pressure. Safety outcomes focused on adverse event rates. Meta-analyses were performed, and risk of bias was assessed using the Cochrane Risk-of-Bias tool version 2. : Fourteen RCTs involving 14,713 patients were included. Tirzepatide significantly increased the proportion of participants achieving weight loss targets, and reduced body weight, waist circumference, HbA1c, and blood pressure versus placebo and insulin. Compared with GLP-1 RAs, tirzepatide provided comparable or better outcomes in weight loss, waist circumference, and glycemic control. The incidence of gastrointestinal adverse events was significantly higher at all doses of tirzepatide compared to placebo and insulin. When compared with GLP-1 RAs, higher doses of tirzepatide were associated with increased risk of nausea, diarrhea, and decreased appetite, but not vomiting. Tirzepatide is an effective option for managing weight and improving metabolic outcomes in patients with T2D or obesity. However, it is associated with an increased risk of gastrointestinal adverse events, especially at higher doses. Therefore, close monitoring should be considered in clinical practice. : PROSPERO CRD42021283449.
肥胖和2型糖尿病(T2D)是主要的公共卫生问题。替尔泊肽在最近的临床试验中显示出了前景。本系统评价和荟萃分析旨在评估替尔泊肽在肥胖或2型糖尿病成人患者中与安慰剂、胰高血糖素样肽-1受体激动剂(GLP-1 RAs)和胰岛素相比的疗效和安全性。于2024年1月17日检索了PubMed、Embase和Cochrane图书馆,重点关注II期和III期随机对照试验(RCT)。我们纳入了涉及T2D或肥胖成人的研究,比较了替尔泊肽与安慰剂、GLP-1 RAs或胰岛素。主要结局是体重减轻目标达到≥5%、≥10%和≥15%的参与者比例。次要结局包括体重、腰围、糖化血红蛋白(HbA1c)水平和血压的变化。安全性结局关注不良事件发生率。进行了荟萃分析,并使用Cochrane偏倚风险工具第2版评估偏倚风险。纳入了14项涉及14713名患者的RCT。与安慰剂和胰岛素相比,替尔泊肽显著提高了达到体重减轻目标的参与者比例,并降低了体重、腰围、HbA1c和血压。与GLP-1 RAs相比,替尔泊肽在体重减轻、腰围和血糖控制方面提供了相当或更好的结果。与安慰剂和胰岛素相比,替尔泊肽所有剂量的胃肠道不良事件发生率均显著更高。与GLP-1 RAs相比,高剂量替尔泊肽与恶心、腹泻风险增加和食欲下降相关,但与呕吐无关。替尔泊肽是治疗T2D或肥胖患者体重和改善代谢结局的有效选择。然而,它与胃肠道不良事件风险增加相关,尤其是高剂量时。因此,在临床实践中应考虑密切监测。:PROSPERO CRD42021283449