首页> 外文期刊>Diabetes care >The efficacy and safety of insulin degludec given in variable once-daily dosing intervals compared with insulin glargine and insulin degludec dosed at the same time daily: A 26-week, randomized, open-label, parallel-group, treat-to-target trial in individuals with type 2 diabetes
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The efficacy and safety of insulin degludec given in variable once-daily dosing intervals compared with insulin glargine and insulin degludec dosed at the same time daily: A 26-week, randomized, open-label, parallel-group, treat-to-target trial in individuals with type 2 diabetes

机译:与每日一次同时给药的甘精胰岛素和地格列松胰岛素相比,以每天一次的可变给药间隔给予地格列松胰岛素的疗效和安全性:一项为期26周,随机,开放标签,平行组,以治疗为目标的试验在2型糖尿病患者中

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OBJECTIVE-The requirement to inject current basal insulin analogs at a fixed time each daymay complicate adherence and compromise glycemic control. This trial evaluated the efficacy and safety of varying the daily injection time of insulin degludec (IDeg), an ultra-long-acting basal insulin. RESEARCH DESIGN AND METHODS-This 26-week, open-label, treat-to-target trial enrolled adults (??18 years) with type 2 diabetes who were either insulin na?ve and receiving oral antidiabetic drugs (OADs) (HbA1c = 7-11%) or previously on basal insulin ?? OAD(s) (HbA1c = 7-10%). Participants were randomized to 1) once-daily (OD) IDeg in a prespecified dosing schedule, creating 8-40-h intervals between injections (IDeg OD Flex; n = 229); 2) once-daily IDeg at the main evening meal (IDegOD; n = 228); or 3) once-daily insulin glargine at the same time each day (IGlarOD; n = 230). The primary outcomewas noninferiority of IDegODFlex to IGlarODinHbA1c reduction after 26 weeks. RESULTS-After 26 weeks, IDeg OD Flex, IDeg OD, and IGlar OD improved HbA1c by 1.28, 1.07, and 1.26% points, respectively (estimated treatment difference [IDeg OD Flex 2 IGlar OD]: 0.04% points [-0.12 to 0.20], confirming noninferiority). No statistically significant differences in overall or nocturnal hypoglycemia were found between IDeg OD Flex and IGlar OD. Comparable glycemic control and rates of hypoglycemia were seen with IDeg OD Flex and IDeg OD. Adverse event profiles were similar across groups. CONCLUSIONS-The use of extreme dosing intervals of 8-40 h demonstrates that the daily injection time of IDeg can be varied without compromising glycemic control or safety. ? 2013 by the American Diabetes Association.
机译:目的-每天在固定时间注射当前基础胰岛素类似物的要求可能会使依从性复杂化并损害血糖控制。该试验评估了改变超长效基础胰岛素degludec(IDeg)每日注射时间的有效性和安全性。研究设计和方法-这项为期26周的,开放标签,针对目标的试验招募了2型糖尿病成年人(未接受胰岛素治疗且接受口服降糖药物(OAD))(HbA1c = 7-11%)或以前使用基础胰岛素? OAD(HbA1c = 7-10%)。参与者被随机分配到1)每天一次(OD)IDeg,按照预先指定的给药时间表,每次注射之间间隔8-40小时(IDeg OD Flex; n = 229); 2)在主要晚餐时段每天一次IDeg(IDegOD; n = 228);或3)每天同一时间每天一次的甘精胰岛素(IGlarOD; n = 230)。主要结局是26周后IDegODFlex与IGlarODinHbA1c降低的非劣效性。结果-26周后,IDeg OD Flex,IDeg OD和IGlar OD分别使HbA1c改善了1.28、1.07和1.26%点(估计治疗差异[IDeg OD Flex 2 IGlar OD]:0.04%点[-0.12至0.20 ],以确认是否自卑)。 IDeg OD Flex和IGlar OD之间的总体或夜间低血糖没有统计学上的显着差异。使用IDeg OD Flex和IDeg OD可观察到可比的血糖控制和低血糖发生率。各组的不良事件情况相似。结论-使用8至40小时的极端给药间隔表明IDeg的每日注射时间可以改变而不会影响血糖控制或安全性。 ? 2013年由美国糖尿病协会颁发。

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