Jastreboff Ania M, le Roux Carel W, Stefanski Adam, Aronne Louis J, Halpern Bruno, Wharton Sean, Wilding John P H, Perreault Leigh, Zhang Shuyu, Battula Ramakrishna, Bunck Mathijs C, Ahmad Nadia N, Jouravskaya Irina
Y-Weight Yale Obesity Research Center, Section of Endocrinology and Metabolism, Department of Medicine, Yale School of Medicine, New Haven, CT.
Section of Pediatric Endocrinology, Department of Pediatrics, Yale School of Medicine, New Haven, CT.
N Engl J Med. 2025 Mar 6;392(10):958-971. doi: 10.1056/NEJMoa2410819. Epub 2024 Nov 13.
Obesity is a chronic disease and causal precursor to myriad other conditions, including type 2 diabetes. In an earlier analysis of the SURMOUNT-1 trial, tirzepatide was shown to provide substantial and sustained reductions in body weight in persons with obesity over a 72-week period. Here, we report the 3-year safety outcomes with tirzepatide and its efficacy in reducing weight and delaying progression to type 2 diabetes in persons with both obesity and prediabetes.
We performed a phase 3, double-blind, randomized, controlled trial in which 2539 participants with obesity, of whom 1032 also had prediabetes, were assigned in a 1:1:1:1 ratio to receive tirzepatide at a once-weekly dose of 5 mg, 10 mg, or 15 mg or placebo. The current analysis involved the participants with both obesity and prediabetes, who received their assigned dose of tirzepatide or placebo for a total of 176 weeks, followed by a 17-week off-treatment period. The three key secondary end points, which were controlled for type I error, were the percent change in body weight from baseline to week 176 and onset of type 2 diabetes during the 176-week and 193-week periods.
At 176 weeks, the mean percent change in body weight among the participants who received tirzepatide was -12.3% with the 5-mg dose, -18.7% with the 10-mg dose, and -19.7% with the 15-mg dose, as compared with -1.3% among those who received placebo (P<0.001 for all comparisons with placebo). Fewer participants received a diagnosis of type 2 diabetes in the tirzepatide groups than in the placebo group (1.3% vs. 13.3%; hazard ratio, 0.07; 95% confidence interval [CI], 0.0 to 0.1; P<0.001). After 17 weeks off treatment or placebo, 2.4% of the participants who received tirzepatide and 13.7% of those who received placebo had type 2 diabetes (hazard ratio, 0.12; 95% CI, 0.1 to 0.2; P<0.001). Other than coronavirus disease 2019, the most common adverse events were gastrointestinal, most of which were mild to moderate in severity and occurred primarily during the dose-escalation period in the first 20 weeks of the trial. No new safety signals were identified.
Three years of treatment with tirzepatide in persons with obesity and prediabetes resulted in substantial and sustained weight reduction and a markedly lower risk of progression to type 2 diabetes than that with placebo. (Funded by Eli Lilly; SURMOUNT-1 ClinicalTrials.gov number, NCT04184622.).
肥胖是一种慢性疾病,也是包括2型糖尿病在内的众多其他疾病的病因先兆。在对SURMOUNT-1试验的早期分析中,替尔泊肽在72周内使肥胖患者的体重显著且持续下降。在此,我们报告替尔泊肽的3年安全性结果及其在降低肥胖合并糖尿病前期患者体重和延缓2型糖尿病进展方面的疗效。
我们进行了一项3期双盲随机对照试验,将2539名肥胖参与者(其中1032人还患有糖尿病前期)按1:1:1:1的比例分配,分别接受每周一次剂量为5毫克、10毫克或15毫克的替尔泊肽或安慰剂。当前分析涉及肥胖合并糖尿病前期的参与者,他们接受分配剂量的替尔泊肽或安慰剂共176周,随后是17周的停药期。三个关键次要终点(已对I型错误进行控制)是从基线到第176周体重的百分比变化以及在176周和193周期间2型糖尿病的发病情况。
在第176周时,接受替尔泊肽治疗的参与者中,5毫克剂量组体重的平均百分比变化为-12.3%,10毫克剂量组为-18.7%,15毫克剂量组为-19.7%,而接受安慰剂组为-1.3%(与安慰剂组的所有比较P<0.001)。替尔泊肽组被诊断为2型糖尿病的参与者少于安慰剂组(1.3%对13.3%;风险比,0.07;95%置信区间[CI],0.0至0.1;P<0.001)。在停药或停用安慰剂17周后,接受替尔泊肽治疗的参与者中有2.4%患有2型糖尿病,接受安慰剂治疗的参与者中有13.7%患有2型糖尿病(风险比,0.12;95%CI,0.1至0.2;P<0.001)。除2019冠状病毒病外,最常见的不良事件是胃肠道事件,其中大多数严重程度为轻度至中度,主要发生在试验前20周的剂量递增期。未发现新的安全信号。
肥胖合并糖尿病前期患者使用替尔泊肽治疗三年可显著且持续减轻体重,与安慰剂相比,进展为2型糖尿病的风险显著降低。(由礼来公司资助;SURMOUNT-1临床试验注册号,NCT04184622。)