Evaluating the efficacy and safety of survodutide for obesity: a systematic review and meta-analysis of randomized controlled trials.

Q3 Medicine
Baylor University Medical Center Proceedings Pub Date : 2025-04-01 eCollection Date: 2025-01-01 DOI:10.1080/08998280.2025.2480512
Abdelaziz A Awad, Alaa Abdrabou Abouelmagd, Fatma Mohammed, Abdelrahman M Elettreby, Mohamed Mahmoud Marey, Mohamed A Aldemerdash, Samar M Soliman, Mohamed Mohamed Belal, Hazem Abosheaishaa
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引用次数: 0

Abstract

Background: Glucagon-like peptide-1 (GLP-1) agonists have established their efficacy and safety in the treatment of obesity. In this study, we aimed to assess the efficacy and safety of survodutide, a new GLP-1 agonist.

Methods: We searched PubMed, Web of Science, Scopus, and Cochrane Library databases until May 2024 for randomized controlled trials using survodutide obesity treatment. Continuous data were pooled as standardized mean difference (SMD), while dichotomous data were pooled as risk ratios (RR) with 95% confidence intervals.

Results: There was a significant relative body weight reduction in the survodutide group (SMD: -1.5; 95% CI: -2.05 to -0.95; P < 0.00001). Overall adverse events in the four included studies weren't significantly different between the survodutide group and placebo group (RR: 1.18; 95% CI: 0.98 to 1.41; I 2 = 72%; P = 0.08). Survodutide was associated with a higher risk of developing diarrhea than the placebo group in the four included trials (RR: 1.89; 95% CI: 1.2 to 2.97; I 2=0%; P < 0.00001).

Conclusion: Survodutide effectively reduced relative body weight, absolute body weight, and hemoglobin A1c (P < 0.00001). The incidence of adverse events was comparable between the two groups, while gastrointestinal adverse events were higher in the survodutide group.

评估肥胖的有效性和安全性:随机对照试验的系统回顾和荟萃分析。
背景:胰高血糖素样肽-1 (GLP-1)激动剂在治疗肥胖方面的有效性和安全性已经得到证实。在这项研究中,我们旨在评估一种新的GLP-1激动剂survodutide的有效性和安全性。方法:我们检索PubMed, Web of Science, Scopus和Cochrane图书馆数据库,直到2024年5月,使用生存期肥胖治疗的随机对照试验。连续数据合并为标准化平均差(SMD),二分类数据合并为风险比(RR), 95%置信区间。结果:生存期组患者相对体重明显下降(SMD: -1.5;95% CI: -2.05 ~ -0.95;pi 2 = 72%;p = 0.08)。在四项纳入的试验中,与安慰剂组相比,生存肽组发生腹泻的风险更高(RR: 1.89;95% CI: 1.2 ~ 2.97;我2 = 0%;结论:生存肽能有效降低相对体重、绝对体重和血红蛋白A1c (P
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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
245
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