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胰高血糖素样肽-1受体激动剂在无糖尿病超重/肥胖青少年中的抗肥胖作用及安全性:一项系统评价和荟萃分析。

The Antiobesity Effect and Safety of GLP-1 Receptor Agonist in Overweight/Obese Adolescents Without Diabetes Mellitus: A Systematic Review and Meta-Analysis.

作者信息

Katole Nilesh T, Salankar Harsh V, Khade Ajay M, Kale Jyoti S, Bankar Nandkishor J, Gosavi Punam, Dudhe Bhushan, Mankar Nishikant, Noman Obaid

机构信息

Pharmacology, Government Medical College, Nagpur, IND.

Pharmacology, NKP Salve Institute of Medical Sciences and Research Centre, Nagpur, IND.

出版信息

Cureus. 2024 Aug 6;16(8):e66280. doi: 10.7759/cureus.66280. eCollection 2024 Aug.

Abstract

BACKGROUND

Glucagon-like peptide-1 receptor agonists (GLP-1 RAs), particularly semaglutide, have become the leading anti-obesity drugs for adults, and a similar trend may follow in adolescents with its recent approval for this age group. However, there is a lack of comparative analysis on the weight loss effects and safety of GLP-1 RAs in obese or overweight pediatric and adolescent populations, especially those who are non-diabetic. This systematic review and meta-analysis aim to provide current evidence on the efficacy and safety of GLP-1 RAs as an anti-obesity treatment in obese or overweight non-diabetic pediatric and adolescent populations.

METHOD

We searched electronic databases from inception until January 2024 for randomized controlled trials (RCTs) that analyzed the weight loss effect of GLP-1 receptor agonists in adolescents with obesity or overweight without diabetes mellitus. Search results were screened, and eligible studies were included to perform a systematic review and meta-analysis using the Review Manager (RevMan) computer program Version 5.4.1 (The Cochrane Collaboration, 2020) with a random-effects model. The primary efficacy outcomes were changes in body weight, BMI, and BMI Z-score, while the secondary outcomes were the incidence of gastrointestinal adverse events, treatment discontinuation rate due to adverse events, and incidence of serious adverse events. The mean difference, odds ratio, and 95% confidence interval (CI) were used to present the meta-analysis results. Publication bias was visualized using a funnel plot. The quality of the studies was analyzed using Cochrane's Risk of Bias tool (RoB2).

RESULTS

A total of seven RCTs with 576 adolescent participants were included in the analysis. GLP-1 RAs significantly achieved greater weight loss than placebo, with a mean difference of -4.98 kg (-8.49, -1.46), I² = 99%, p = 0.006. Subgroup analysis showed that semaglutide had the most pronounced anti-obesity effect (mean difference of -17.70 kg (-18.89, -16.51), p < 0.00001), compared to liraglutide (mean difference of -2.26 kg (-5.17, 0.65), I² = 99%, p = 0.13) and exenatide (mean difference of -3.17 kg (-4.45, -1.90), I² = 0%, p < 0.0001). Similar results were obtained for other efficacy parameters such as BMI and BMI z-score. However, GLP-1 RA was associated with more gastrointestinal adverse events (such as nausea and vomiting) than placebo (3.06 (2.12, 4.42), I² = 0%, p < 0.00001), with incidence comparable among all GLP-1 RAs in the subgroup analysis. The overall risk of bias among included studies was either of 'some concern' or 'high risk.'

CONCLUSIONS

Our meta-analysis demonstrated that GLP-1 RAs had a superior anti-obesity effect compared to placebo or lifestyle modification in obese or overweight non-diabetic adolescents, particularly semaglutide, which had a more pronounced anti-obesity effect than liraglutide and exenatide, with tolerable gastrointestinal adverse effects.

摘要

背景

胰高血糖素样肽-1受体激动剂(GLP-1 RAs),尤其是司美格鲁肽,已成为成人主要的抗肥胖药物,随着其最近被批准用于该年龄组,青少年中可能也会出现类似趋势。然而,对于肥胖或超重的儿科及青少年人群,尤其是非糖尿病患者,缺乏关于GLP-1 RAs减肥效果和安全性的比较分析。本系统评价和荟萃分析旨在提供有关GLP-1 RAs作为肥胖或超重非糖尿病儿科及青少年人群抗肥胖治疗的疗效和安全性的当前证据。

方法

我们检索了从数据库建立至2024年1月的电子数据库,以查找分析GLP-1受体激动剂对肥胖或超重且无糖尿病的青少年减肥效果的随机对照试验(RCTs)。对检索结果进行筛选,纳入符合条件的研究,使用Review Manager(RevMan)计算机程序5.4.1版(Cochrane协作网,2020)采用随机效应模型进行系统评价和荟萃分析。主要疗效指标为体重、BMI和BMI Z评分的变化,次要指标为胃肠道不良事件的发生率、因不良事件导致的治疗中断率以及严重不良事件的发生率。荟萃分析结果采用平均差、比值比和95%置信区间(CI)表示。使用漏斗图直观显示发表偏倚。采用Cochrane偏倚风险工具(RoB2)分析研究质量。

结果

共有7项RCTs纳入分析,涉及576名青少年参与者。GLP-1 RAs显著比安慰剂实现了更大程度的体重减轻,平均差为-4.98 kg(-8.49,-1.46),I² = 99%,p = 0.006。亚组分析显示,与利拉鲁肽(平均差为-2.26 kg(-5.17,0.65),I² = 99%,p = 0.13)和艾塞那肽(平均差为-3.17 kg(-4.45,-1.90),I² = 0%,p < 0.0001)相比,司美格鲁肽具有最显著的抗肥胖效果(平均差为-17.70 kg(-18.89,-16.51),p < 0.00001)。其他疗效参数如BMI和BMI Z评分也得到了类似结果。然而,与安慰剂相比,GLP-1 RA与更多的胃肠道不良事件(如恶心和呕吐)相关(3.06(2.12,4.42),I² = 0%,p < 0.00001),亚组分析中所有GLP-1 RAs的发生率相当。纳入研究的总体偏倚风险为“有些担忧”或“高风险”。

结论

我们的荟萃分析表明,在肥胖或超重的非糖尿病青少年中,GLP-1 RAs与安慰剂或生活方式改变相比具有更好的抗肥胖效果,尤其是司美格鲁肽,其抗肥胖效果比利拉鲁肽和艾塞那肽更显著,且胃肠道不良反应可耐受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d27/11376316/018b2fbb6171/cureus-0016-00000066280-i01.jpg

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