Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
AstraZeneca, Gothenburg, Sweden.
Diabetes Obes Metab. 2017 Sep;19(9):1276-1288. doi: 10.1111/dom.12954. Epub 2017 May 31.
Dapagliflozin and exenatide reduce body weight by differing mechanisms. Dual therapy with these agents reduces body weight, adipose tissue volume, glycaemia and systolic blood pressure (SBP) over 24 weeks. Here, we examined these effects over 1 year in obese adults without diabetes.
Obese adults without diabetes (N = 50; aged 18-70 years; body mass index, 30-45 kg/m ) were initially randomized to double-blind oral dapagliflozin 10 mg once daily plus subcutaneous long-acting exenatide 2 mg once weekly or to placebo. They entered an open-label extension from 24 to 52 weeks during which all participants received active treatment.
Of the original 25 dapagliflozin + exenatide-treated and 25 placebo-treated participants, respectively, 21 (84%) and 17 (68%) entered the open-label period and 16 (64%) and 17 (68%) completed 52 weeks of treatment. At baseline, mean body weight was 104.6 kg, and 73.5% of participants had prediabetes (impaired fasting glucose or impaired glucose tolerance). Reductions with dapagliflozin + exenatide at 24 weeks were sustained at 52 weeks, respectively, for body weight (-4.5 and -5.7 kg), total adipose tissue volume (-3.8 and -5.3 L), proportion with prediabetes (34.8% and 35.3%), and SBP (-9.8 and -12.0 mm Hg). Effects on body weight, SBP and glycaemia at 52 weeks with placebo → dapagliflozin + exenatide were similar to those observed with continuation of dapagliflozin + exenatide. Nausea and injection-site reactions were more frequent with dapagliflozin + exenatide than with placebo and diminished over time. Safety and tolerability were similar to that in previous diabetes trials with these agents. No clear difference in adverse event-related withdrawals between placebo and active treatment periods was observed.
Dapagliflozin + exenatide dual therapy produced sustained reductions in body weight, prediabetes and SBP over 52 weeks and was well tolerated in obese adults without diabetes.
达格列净和艾塞那肽通过不同的机制减轻体重。这两种药物的联合治疗可在 24 周内降低体重、脂肪组织体积、血糖和收缩压(SBP)。在这里,我们在没有糖尿病的肥胖成年人中检查了它们在一年中的这些影响。
没有糖尿病的肥胖成年人(N=50;年龄 18-70 岁;体重指数,30-45kg/m )最初随机接受每日口服达格列净 10mg 加每周一次皮下长效艾塞那肽 2mg 或安慰剂的双盲治疗。他们从 24 周进入开放标签扩展期,在此期间所有参与者均接受活性治疗。
在最初的 25 名达格列净+艾塞那肽治疗组和 25 名安慰剂治疗组中,分别有 21 名(84%)和 17 名(68%)进入开放标签期,16 名(64%)和 17 名(68%)完成了 52 周的治疗。基线时,平均体重为 104.6kg,73.5%的参与者患有前驱糖尿病(空腹血糖受损或糖耐量受损)。达格列净+艾塞那肽在 24 周时的减轻分别持续到 52 周,体重分别为(-4.5 和-5.7kg),总脂肪组织体积分别为(-3.8 和-5.3L),前驱糖尿病的比例分别为(34.8%和 35.3%),SBP 分别为(-9.8 和-12.0mmHg)。在 52 周时,安慰剂→达格列净+艾塞那肽对体重、SBP 和血糖的影响与继续使用达格列净+艾塞那肽相似。与安慰剂相比,达格列净+艾塞那肽更频繁地出现恶心和注射部位反应,且随时间推移而减少。安全性和耐受性与这些药物在之前的糖尿病试验中相似。在安慰剂和活性治疗期间,未观察到与不良事件相关的停药率有明显差异。
达格列净+艾塞那肽联合治疗可在 52 周内持续降低体重、前驱糖尿病和 SBP,且在没有糖尿病的肥胖成年人中耐受性良好。