Dallas Diabetes and Endocrine Center at Medical City, Dallas, Texas, USA.
Diabetes Care. 2010 Jun;33(6):1173-5. doi: 10.2337/dc09-1203. Epub 2010 Mar 23.
To assess the effects of exenatide on body weight and glucose tolerance in nondiabetic obese subjects with normal or impaired glucose tolerance (IGT) or impaired fasting glucose (IFG).
Obese subjects (n = 152; age 46 +/- 12 years, female 82%, weight 108.6 +/- 23.0 kg, BMI 39.6 +/- 7.0 kg/m(2), IGT or IFG 25%) were randomized to receive exenatide (n = 73) or placebo (n = 79), along with lifestyle intervention, for 24 weeks. RESULTS Exenatide-treated subjects lost 5.1 +/- 0.5 kg from baseline versus 1.6 +/- 0.5 kg with placebo (exenatide--placebo, P < 0.001). Placebo-subtracted difference in percent weight reduction was -3.3 +/- 0.5% (P < 0.001). Both groups reduced their daily calorie intake (exenatide, -449 cal; placebo, -387 cal). IGT or IFG normalized at end point in 77 and 56% of exenatide and placebo subjects, respectively.
Exenatide plus lifestyle modification decreased caloric intake and resulted in weight loss in nondiabetic obesity with improved glucose tolerance in subjects with IGT and IFG.
评估艾塞那肽对糖耐量正常或受损(IGT)或空腹血糖受损(IFG)的非糖尿病肥胖患者体重和葡萄糖耐量的影响。
肥胖受试者(n = 152;年龄 46 +/- 12 岁,女性 82%,体重 108.6 +/- 23.0 kg,BMI 39.6 +/- 7.0 kg/m(2),IGT 或 IFG 占 25%)随机接受艾塞那肽(n = 73)或安慰剂(n = 79)治疗,并进行生活方式干预,共 24 周。结果:艾塞那肽治疗组体重从基线下降 5.1 +/- 0.5 kg,安慰剂组下降 1.6 +/- 0.5 kg(艾塞那肽-安慰剂,P < 0.001)。体重减轻的百分比差值为-3.3 +/- 0.5%(P < 0.001)。两组均减少了每日卡路里摄入量(艾塞那肽,-449 cal;安慰剂,-387 cal)。IGT 或 IFG 在终点时分别有 77%和 56%的艾塞那肽和安慰剂受试者正常化。
艾塞那肽联合生活方式改变可减少热量摄入,并导致非糖尿病肥胖患者体重减轻,IGT 和 IFG 患者的葡萄糖耐量得到改善。