Institute of Therapeutic Innovations and Outcomes (ITIO), College of Pharmacy, The Ohio State University, 500 West 12th Ave., Columbus, OH, 43210, USA.
Department of Bariatric and Metabolic Surgery, Fudan University Affiliated Huadong Hospital, Shanghai, China.
Int J Clin Pharm. 2024 Dec;46(6):1268-1280. doi: 10.1007/s11096-024-01779-x. Epub 2024 Jul 22.
Tirzepatide was approved to treat type 2 diabetes and obesity, but its efficacy and safety in patients without diabetes has not been investigated.
This meta-analysis aimed to evaluate the efficacy and safety of tirzepatide compared to placebo in overweight or obese patients without diabetes.
PubMed, Embase and Cochrane were searched on January 18, 2024. Randomized controlled trials (RCTs) that used tirzepatide in overweight or obese adults without diabetes were included. Efficacy outcomes included the proportion of participants achieving weight loss targets, changes in body weight (%), body mass index (BMI), waist circumference (WC), and blood pressure (BP). Safety outcomes were commonly reported adverse events. Standardized mean differences (SMD) or odds ratios (OR) with 95% confidence intervals (CIs) were used for continuous and dichotomous outcomes, respectively.
Three RCTs with 3901 participants were included. Tirzepatide was associated with increased proportion of participants achieving weight loss targets, reduced body weight (SMD - 1.61, 95% CI - 2.20 to - 1.02), BMI (SMD - 2.13, 95% CI - 3.08 to - 1.18), WC (SMD - 0.91, 95% CI - 1.14 to - 0.69), and BP versus placebo. However, the risk of adverse events such as nausea (OR 4.26, 95% CI 2.60 to 3.81), vomiting (OR 8.35, 95% CI 5.19 to 13.45), and diarrhea (OR 3.57, 95% CI 2.80 to 4.57) was significantly higher for tirzepatide versus placebo.
Tirzepatide significantly reduced weight and improved metabolic markers among overweight or obese without diabetes. However, increased adverse events highlights the need for benefits versus risks assessment before initiation and continuous monitoring.
替西帕肽已被批准用于治疗 2 型糖尿病和肥胖症,但尚未研究其在无糖尿病患者中的疗效和安全性。
本荟萃分析旨在评估与安慰剂相比,替西帕肽在超重或肥胖且无糖尿病的患者中的疗效和安全性。
于 2024 年 1 月 18 日检索 PubMed、Embase 和 Cochrane 数据库。纳入使用替西帕肽治疗超重或肥胖且无糖尿病的成年人的随机对照试验(RCT)。疗效结局包括达到体重减轻目标的参与者比例、体重变化(%)、体重指数(BMI)、腰围(WC)和血压(BP)。安全性结局为常见不良事件报告。连续结局采用标准化均数差(SMD),二分类结局采用比值比(OR)及其 95%置信区间(CI)。
纳入 3 项 RCT,共计 3901 名参与者。与安慰剂相比,替西帕肽可增加达到体重减轻目标的参与者比例,降低体重(SMD -1.61,95%CI -2.20 至 -1.02)、BMI(SMD -2.13,95%CI -3.08 至 -1.18)、WC(SMD -0.91,95%CI -1.14 至 -0.69)和 BP。然而,替西帕肽组恶心(OR 4.26,95%CI 2.60 至 3.81)、呕吐(OR 8.35,95%CI 5.19 至 13.45)和腹泻(OR 3.57,95%CI 2.80 至 4.57)等不良事件的风险显著高于安慰剂组。
替西帕肽可显著降低超重或肥胖且无糖尿病患者的体重并改善代谢标志物。然而,不良事件的增加突出表明在开始治疗前和持续监测时需要评估获益与风险。