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Effects of saxagliptin add-on therapy to insulin on blood glycemic fluctuations in patients with type 2 diabetes: A randomized, control, open-labeled trial

机译:沙格列汀联合胰岛素治疗对2型糖尿病患者血糖波动的影响:一项随机对照开放性试验

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Background:To investigate whether saxagliptin add-on therapy to continuous subcutaneous insulin infusion (CSII) further improve blood glycemic control than CSII therapy in patients with newly diagnosed type 2 diabetes (T2D).Methods:This was a single-center, randomized, control, open-labeled trial. Newly diagnosed T2D patients were recruited between February 2014 and December 2015. Subjects were divided into saxagliptin add-on therapy to CSII group (n = 31) and CSII therapy group (n = 38). The treatment was maintained for 4 weeks. Oral glucose tolerance test was performed at baseline. Serum samples were obtained before and 30 and 120minutes after oral administration for glucose, insulin, and C-peptide determination. Continuous glucose monitoring (CGM) was performed before and endpoint.Results:A total of 69 subjects were admitted. After 4-week therapy, CGM data showed that patients with saxagliptin add-on therapy exhibited further improvement of mean amplitude glycemic excursion (MAGE), the incremental area under curve of plasma glucose >7.8 and 10mmol/L compared with that of control group. In addition, the hourly mean blood glucose concentrations, especially between 0000 and 0600 in patient with saxagliptin add-on therapy, were significantly lower compared with that of the control patients. Furthermore, patients in saxagliptin add-on group needed lower insulin dose to maintain euglycemic control. In addition, severe hypoglycemic episode was not observed from any group.Conclusion:Saxagliptin add-on therapy to insulin had the ability of further improve blood glycemic controlling, with lower insulin dose required by patients with T2D to maintain euglycemic controlling.
机译:背景:研究沙格列汀联合皮下胰岛素输注(CSII)疗法是否比CSII疗法进一步改善了新诊断的2型糖尿病(T2D)患者的血糖控制。方法:这是一种单中心,随机,对照,开放标签的试验。在2014年2月至2015年12月之间招募了新诊断的T2D患者。受试者被分为CSII组(n = 31)和CSII治疗组(n = 38)的沙格列汀附加疗法。维持治疗4周。在基线时进行口服葡萄糖耐量测试。在口服之前以及口服后30和120分钟获得血清样品,用于测定葡萄糖,胰岛素和C肽。结果:共有69名受试者被纳入研究。经过4周的治疗后,CGM数据显示,沙格列汀联合治疗患者的平均幅度血糖偏移(MAGE)进一步改善,血浆葡萄糖曲线下的增加面积与对照组相比增加了> 7.8和10mmol / L。此外,沙格列汀联合疗法患者的每小时平均血糖浓度,特别是在0000至0600之间,显着低于对照组。此外,沙格列汀联合治疗组的患者需要降低胰岛素剂量以维持正常的血糖控制。此外,任何一组均未观察到严重的降血糖事件。结论:沙格列汀胰岛素联合治疗具有进一步改善血糖控制的能力,T2D患者维持正常血糖控制所需的胰岛素剂量较低。

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