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Efficacy and tolerability of exenatide monotherapy in obese patients with newly diagnosed type 2 diabetes: a randomized, 26weeks metformin-controlled, parallel-group study

机译:艾塞那肽单药治疗肥胖的新诊断2型糖尿病患者的疗效和耐受性:一项随机,26周,以二甲双胍为对照的平行组研究

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摘要

Background Incretin-based therapies provide additional options for treating type 2 diabetes.We aimed to evaluate the efficacy and tolerability of exenatide monotherapy in obese patients with type 2 diabetes.Methods A 26-week,mefformin controlled,parallel-group study was conducted among antidiabetic drug-naive obese patients aged >18 years,and with type 2 diabetes.Participating patients were randomly assigned to receive exenatide or metformin treatments.Results Fifty-nine patients (age (50.5±8.6) years,body mass index (BMI) (30.2±1.6) kg/m2,and hemoglobin A1C (HbA1c (8.2±1.2)%) were enrolled in the study.Glucose control and weight reduction improved in both groups receiving treatment.HbA1c and oral glucose tolerance test (OGTT) 2 hour glycemia reduction with exenatide was superior to that obtained with mefformin ((-2.10±1.79)% vs.(-1.66±1.38)%,(-5.11±2.68) mmol/L vs.(-2.80±2.70) mmol/L,P <0.05).Fast plasma glucose (FPG) reduction was not significantly different between the two groups ((-1.8±2.0) mmol/L vs.(-1.6±1.7) mmol/L,P >0.05).Patients treated with exenatide achieved HbA1c of <7% (97% of patients) and <6.5% (79%)at end-point,vs.93% and 73% with metformin (P >0.05).Greater weight reduction was also achieved with exenatide ((-5.80±3.66) kg) than with metformin ((-3.81±1.38) kg,P <0.01).Homeostasis model assessment of beta-cell function (HOMA-B) was not significantly increased,but the insulinogenic index and HOMA for insulin sensitivity (HOMA-S) were greatly improved in the exenatide group (P <0.05).Nausea was the most common adverse effect in exenatide treatment (30% vs.8%; P <0.05),but most cases were of mild to moderate intensity.One case in the exenatide group was withdrawn earlrly because of severe nausea.Hypoglycemia events were often observed during the first 4 weeks,with 12%of patients in the exenatide and 3.2% in metformin groups,respectively (P <0.05).No incidents of severe hypoglycemia were reported.Conclusions Exenatide demonstrated more beneficial effects on HbA1c.weight reduction and insulin resistance during 26 weeks of treatment,but there were more hypoglycemic events and mild-to-moderate nausea compared with metformin.These results suggested that exenatide monotherapy may provide a viable treatment option in newly developed type 2 diabetes.
机译:背景基于肠泌素的疗法为治疗2型糖尿病提供了其他选择。我们旨在评估艾塞那肽单一疗法在肥胖2型糖尿病患者中的疗效和耐受性。方法在26周的二甲双胍对照,平行组研究中进行了抗糖尿病药研究年龄大于18岁且未接受过药物治疗的肥胖患者,并伴有2型糖尿病。参与研究的患者被随机分配接受艾塞那肽或二甲双胍治疗。结果59例患者(年龄(50.5±8.6)岁,体重指数(BMI)(30.2)研究纳入±1.6)kg / m2和血红蛋白A1C(HbA1c(8.2±1.2)%)。接受治疗的两组患者血糖控制和体重减轻均得到改善。HbA1c和口服葡萄糖耐量试验(OGTT)降低2小时血糖艾塞那肽的治疗效果优于二甲双胍((-2.10±1.79)%vs。(-1.66±1.38)%,(-5.11±2.68)mmol / L vs。(-2.80±2.70)mmol / L,P < 0.05)。两组之间的快速血浆葡萄糖(FPG)降低没有显着差异(( -1.8±2.0)mmol / L vs。(-1.6±1.7)mmol / L,P> 0.05)。艾塞那肽治疗的患者在HbA1c达到<7%(97%的患者)和<6.5%(79%)。终点,与二甲双胍相比(93%和73%)(P> 0.05)。艾塞那肽((-5.80±3.66)kg)的体重减轻也比二甲双胍((-3.81±1.38)kg的体重减轻,P < 0.01)。艾塞那肽组的β细胞功能(HOMA-B)稳态模型评估没有显着增加,但致胰岛素指数和HOMA对胰岛素敏感性(HOMA-S)显着改善(P <0.05)。艾塞那肽治疗中最常见的不良反应(30%vs.8%); P <0.05),但多数病例为轻度至中度。艾塞那肽组中有1例因严重恶心而早退出。在前4周经常观察到低血糖事件,艾塞那肽组患者占12%,3.2二甲双胍组分别为%(P <0.05)。未报告严重的低血糖事件。结论艾塞那肽在治疗26周期间显示出对HbA1c减轻体重和胰岛素抵抗的有益作用,但出现更多的降血糖事件和轻度与二甲双胍相比,中度恶心。这些结果表明,艾塞那肽单药治疗可能为新近发展的2型糖尿病提供可行的治疗选择。

著录项

  • 来源
    《中华医学杂志(英文版)》 |2012年第15期|2677-2681|共5页
  • 作者单位

    Department of Endocrinology, Peking University First Hospital,Beijing 100034, China;

    Huguosi Hospital of Traditional Chinese Medicine, Beijing University of Chinese Medicine and Pharmacology, Beijing 100035, China;

    Department of Endocrinology, Peking University First Hospital,Beijing 100034, China;

    Department of Endocrinology, Peking University First Hospital,Beijing 100034, China;

    Department of Endocrinology, Peking University First Hospital,Beijing 100034, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 chi
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