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首页> 外文期刊>Diabetes, obesity & metabolism >Interim analysis of the effects of exenatide treatment on A1C, weight and cardiovascular risk factors over 82 weeks in 314 overweight patients with type 2 diabetes.
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Interim analysis of the effects of exenatide treatment on A1C, weight and cardiovascular risk factors over 82 weeks in 314 overweight patients with type 2 diabetes.

机译:对314名2型糖尿病超重患者进行82周艾塞那肽治疗对A1C,体重和心血管危险因素的影响的中期分析。

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Aim: Exenatide, an incretin mimetic for the adjunct treatment of type 2 diabetes (DM2), reduced A1C and weight in 30-week placebo-controlled trials. This analysis examined the effects of exenatide on glycaemic control and weight over an 82-week period in patients with DM2 unable to achieve adequate glycaemic control with sulphonylurea (SU) and/or metformin (MET). Methods: This interim analysis is of 314 patients who received exenatide in the 30-week placebo-controlled trials and subsequently in 52 weeks of open-label uncontrolled extension studies for 82 weeks of exenatide in total. Patients continued their SU and/or MET regimens throughout. Results: Patients completed 82 weeks of exenatide treatment [n = 314, 63% M, age 56 +/- 10 years, weight 99 +/- 21 kg, body mass index 34 +/- 6 kg/m(2), A1C 8.3 +/- 1.0% (mean +/- SD)]. Reduction in A1C from baseline to week 30 [-0.9 +/- 0.1% (mean +/- SE)] was sustained to week 82 (-1.1 +/- 0.1%), with 48% of patients achieving A1C
机译:目的:艾塞那肽,一种肠降血糖素模拟物,用于辅助治疗2型糖尿病(DM2),在30周的安慰剂对照试验中降低了A1C和体重。该分析检查了艾塞那肽对82岁以下无法通过磺脲类(SU)和/或二甲双胍(MET)进行充分血糖控制的DM2患者的血糖控制和体重的影响。方法:这项中期分析是在30周的安慰剂对照试验中对314名接受艾塞那肽治疗的患者进行的,随后在52周的开放标签非对照扩展研究中接受了艾塞那肽的总共82周。患者在整个过程中继续其SU和/或MET方案。结果:患者完成艾塞那肽治疗82周[n = 314,男63%M,年龄56 +/- 10岁,体重99 +/- 21 kg,体重指数34 +/- 6 kg / m(2),A1C 8.3 +/- 1.0%(平均值+/- SD)]。从基线到第30周A1C降低[-0.9 +/- 0.1%(平均+/- SE)]持续至第82周(-1.1 +/- 0.1%),其中48%的患者达到A1C

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