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首页> 外文期刊>Diabetes therapy >Bedtime-to-Morning Glucose Difference and iGlarLixi in Type 2 Diabetes: Post Hoc Analysis of LixiLan-L
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Bedtime-to-Morning Glucose Difference and iGlarLixi in Type 2 Diabetes: Post Hoc Analysis of LixiLan-L

机译:2型糖尿病患者睡前至早上的血糖差异和iGlarLixi:LixiLan-L的事后分析

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IntroductionA difference of?≥?50–55?mg/dL between bedtime and morning glucose (BeAM) values in patients with type 2 diabetes (T2D) on basal insulin is an indicator of poor postprandial glucose control. This analysis compared the effect of treatment with a fixed-ratio combination of insulin glargine/lixisenatide (iGlarLixi) vs insulin glargine (iGlar) on BeAM values, and evaluated the impact of BeAM values on glycemic and safety endpoints. MethodsIn this post hoc analysis of 517 participants from the LixiLan-L trial, change in BeAM values and composite efficacy and safety endpoints stratified by BeAM value ?55?mg/dL or ≥?55?mg/dL were evaluated in patients with T2D uncontrolled on basal insulin randomized to iGlarLixi or iGlar over 30?weeks (LixiLan-L). ResultsGreater reductions in BeAM values were seen with iGlarLixi vs iGlar, and a higher proportion of patients reached a BeAM value ?55?mg/dL in the iGlarLixi arm. A BeAM value ?55?mg/dL was associated with improved glycemic control, lower risk of hypoglycemia, and a greater proportion of patients achieving glycemic targets without hypoglycemia or weight gain. Greater reductions in BeAM values were seen with iGlarLixi vs iGlar, irrespective of stratification by glycated hemoglobin A1c or glycemic endpoints. ConclusionsGreater reductions in bedtime-to-morning glucose differential, or BeAM, were observed with iGlarLixi vs iGlar in patients with T2D uncontrolled on basal insulin, reflecting better overall control of both fasting and prandial glucose and more appropriate matching of therapy to physiologic needs. Trial RegistrationClinicalTrials.gov Identifier NCT02058160. FundingSanofi US, Inc.
机译:前言基础胰岛素治疗的2型糖尿病(T2D)患者的就寝时间和早晨葡萄糖(BeAM)值之间的差≥≥50-55?mg / dL,是餐后血糖控制不良的指标。该分析比较了固定比例的甘精胰岛素/立克塞奈肽(iGlarLixi)与甘精胰岛素(iGlar)组合对BeAM值的治疗效果,并评估了BeAM值对血糖和安全终点的影响。方法在这项对LixiLan-L试验的517名参与者的事后分析中,评估了2型糖尿病患者BeAM值的变化以及以BeAM值<?55?mg / dL或≥?55?mg / dL分层的复合功效和安全性终点在30周内随机分配给iGlarLixi或iGlar的基础胰岛素不受控制(LixiLan-L)。结果与iGlar相比,iGlarLixi组的BeAM值降低幅度更大,并且iGlarLixi组的BeAM值<?55?mg / dL的患者比例更高。 BeAM值<?55?mg / dL与改善血糖控制,降低低血糖风险和实现更大血糖目标而无低血糖或体重增加的患者有关。与糖化血红蛋白A1c或血糖终点分层无关,iGlarLixi与iGlar相比BeAM值有更大降低。结论在不受基础胰岛素控制的T2D患者中,使用iGlarLixi和iGlar可以观察到早晨床间血糖差异(BeAM)的更大降低,这反映了对空腹和餐后血糖的总体控制更好,并且疗法更适合生理需求。试用注册ClinicalTrials.gov标识符NCT02058160。资金赛诺菲美国有限公司

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