Efficacy and safety of tirzepatide versus placebo in overweight or obese adults without diabetes: a systematic review and meta-analysis of randomized controlled trials.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Ligang Liu, Hekai Shi, Merilyn Xie, Yuxiao Sun, Milap C Nahata
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引用次数: 0

Abstract

Background: Tirzepatide was approved to treat type 2 diabetes and obesity, but its efficacy and safety in patients without diabetes has not been investigated.

Aim: This meta-analysis aimed to evaluate the efficacy and safety of tirzepatide compared to placebo in overweight or obese patients without diabetes.

Method: 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.

Results: 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.

Conclusion: 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.

Abstract Image

对无糖尿病的超重或肥胖成人服用替扎帕肽与安慰剂的疗效和安全性:随机对照试验的系统回顾和荟萃分析。
背景:目的:本荟萃分析旨在评估与安慰剂相比,替扎帕肽对无糖尿病的超重或肥胖患者的疗效和安全性:方法:于 2024 年 1 月 18 日检索了 PubMed、Embase 和 Cochrane。研究纳入了对无糖尿病的超重或肥胖成人使用替扎帕肽的随机对照试验(RCT)。疗效结果包括达到减重目标的参与者比例、体重变化(%)、体重指数(BMI)、腰围(WC)和血压(BP)。安全性结果为通常报告的不良事件。连续结果和二分结果分别采用标准化平均差(SMD)或带 95% 置信区间(CIs)的几率比(OR):结果:共纳入了三项 RCT,共有 3901 名参与者。与安慰剂相比,替扎帕肽可增加达到减重目标的参与者比例,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)和血压。然而,与安慰剂相比,替西帕肽发生恶心(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)等不良事件的风险明显更高:结论:在无糖尿病的超重或肥胖患者中,替扎帕肽可明显减轻体重并改善代谢指标。结论:替唑帕肽能明显减轻无糖尿病的超重或肥胖患者的体重并改善代谢指标,但不良事件的增加凸显了在用药前进行效益与风险评估和持续监测的必要性。
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来源期刊
CiteScore
4.10
自引率
8.30%
发文量
131
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacy (IJCP) offers a platform for articles on research in Clinical Pharmacy, Pharmaceutical Care and related practice-oriented subjects in the pharmaceutical sciences. IJCP is a bi-monthly, international, peer-reviewed journal that publishes original research data, new ideas and discussions on pharmacotherapy and outcome research, clinical pharmacy, pharmacoepidemiology, pharmacoeconomics, the clinical use of medicines, medical devices and laboratory tests, information on medicines and medical devices information, pharmacy services research, medication management, other clinical aspects of pharmacy. IJCP publishes original Research articles, Review articles , Short research reports, Commentaries, book reviews, and Letters to the Editor. International Journal of Clinical Pharmacy is affiliated with the European Society of Clinical Pharmacy (ESCP). ESCP promotes practice and research in Clinical Pharmacy, especially in Europe. The general aim of the society is to advance education, practice and research in Clinical Pharmacy . Until 2010 the journal was called Pharmacy World & Science.
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