Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, Montreal, Canada; Division of Experimental Medicine, McGill University, Montreal, Canada.
Division of Cardiac Surgery, Department of Surgery, McGill University, Montreal, Canada.
Am J Cardiol. 2024 Jul 1;222:121-130. doi: 10.1016/j.amjcard.2024.04.041. Epub 2024 Apr 26.
Semaglutide, a glucagon-like peptide-1 receptor agonist, has demonstrated clinically important weight loss effects in patients with type 2 diabetes. However, its effects on sustained weight loss in patients without diabetes remains unclear. Our objective was to examine the long-term efficacy and safety of semaglutide use for weight loss in patients with overweight/obesity and without diabetes. MEDLINE, EMBASE, and the Cochrane Libraries were systematically searched to identify randomized controlled trials that randomized participants with overweight/obesity and without diabetes to once-weekly 2.4 mg subcutaneous semaglutide versus placebo, with a follow-up of at least 68 weeks. The primary outcome was a change in relative body weight from baseline to the longest follow-up. Random-effects models with inverse variance weighting were used to estimate the weighted mean differences (WMDs) and relative risks (RRs) with 95% confidence intervals (CIs). A total of 4 randomized controlled trials (n = 3,087) were included. Of the 3 trials that provided body mass index by category (n = 2,783), 94.0% of the participants had a baseline body mass index ≥30 kg/m. Compared with placebo, the use of semaglutide was associated with substantial decreases in long-term relative (WMD -12.1%, 95% CI -13.5 to -10.7) and absolute body weight (WMD -12.3 kg, 95% CI -13.6 to -11.0). At the longest follow-up, 33.4% of participants randomized to semaglutide achieved ≥20% weight loss compared with 2.2% with placebo (RR 15.08, 95% CI 9.31 to 24.43). The risk of gastrointestinal adverse events was higher in participants who took semaglutide than placebo (RR 1:47, 95% CI 1.28 to 1.68); however, the majority of these events were transient and mild-to-moderate in severity and did not require treatment discontinuation. In conclusion, semaglutide is efficacious for sustained weight loss in patients with overweight/obesity and without diabetes.
司美格鲁肽是一种胰高血糖素样肽-1 受体激动剂,已在 2 型糖尿病患者中显示出具有临床重要意义的减重效果。然而,其在无糖尿病患者中的持续减重效果尚不清楚。我们的目的是研究司美格鲁肽用于超重/肥胖且无糖尿病患者的减肥的长期疗效和安全性。系统检索了 MEDLINE、EMBASE 和 Cochrane 图书馆,以确定将超重/肥胖且无糖尿病的参与者随机分为每周一次皮下注射 2.4mg 司美格鲁肽与安慰剂组,随访至少 68 周的随机对照试验。主要结局为从基线到最长随访时的相对体重变化。使用具有倒数方差加权的随机效应模型来估计加权均数差值(WMD)和相对风险(RR)及其 95%置信区间(CI)。共纳入 4 项随机对照试验(n=3087)。在提供按类别分类的体重指数的 3 项试验中(n=2783),94.0%的参与者基线体重指数≥30kg/m。与安慰剂相比,司美格鲁肽的使用与长期相对体重(WMD-12.1%,95%CI-13.5 至-10.7)和绝对体重(WMD-12.3kg,95%CI-13.6 至-11.0)的显著下降相关。在最长随访时,与安慰剂相比,33.4%随机接受司美格鲁肽的参与者达到了≥20%的体重减轻(RR 15.08,95%CI 9.31 至 24.43)。与安慰剂相比,接受司美格鲁肽的参与者胃肠道不良事件的风险更高(RR 1:47,95%CI 1.28 至 1.68);然而,这些事件大多数是短暂的,严重程度为轻度至中度,不需要停止治疗。总之,司美格鲁肽对超重/肥胖且无糖尿病的患者的持续减重是有效的。