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Combining insulin with metformin or an insulin secretagogue in non-obese patients with type 2 diabetes: 12 month randomised double blind trial

机译:在非肥胖2型糖尿病患者中将胰岛素与二甲双胍或胰岛素促分泌剂联合使用:12个月随机双盲试验

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摘要

>Objectives To study the effect of insulin treatment in combination with metformin or an insulin secretagogue, repaglinide, on glycaemic regulation in non-obese patients with type 2 diabetes.>Design Randomised, double blind, double dummy, parallel trial. >Setting Secondary care in Denmark between 2003 and 2006.>Participants Non-obese patients (BMI ≤27) with preserved beta cell function. >Interventions After a four month run-in period with repaglinide plus metformin combination therapy, patients with a glycated haemoglobin (HbA1c) concentration of 6.5% or more were randomised to repaglinide 6 mg or metformin 2000 mg. All patients also received biphasic insulin aspart 70/30 (30% soluble insulin aspart and 70% intermediate acting insulin aspart) 6 units once a day before dinner for 12 months. Insulin dose was adjusted aiming for a fasting plasma glucose concentration of 4.0-6.0 mmol/l. The target of HbA1c concentration was less than 6.5%. Treatment was intensified to two or three insulin injections a day if glycaemic targets were not reached.>Main outcome measure HbA1c concentration.>Results Of the 459 patients who were eligible, 102 were randomised, and 97 completed the trial. Patients had had type 2 diabetes for approximately 10 years. At the end of treatment, HbA1c concentration was reduced by a similar amount in the two treatment groups (insulin plus metformin: mean (standard deviation) HbA1c 8.15% (1.32) v 6.72% (0.66); insulin plus repaglinide: 8.07% (1.49) v 6.90% (0.68); P=0.177). Total daily insulin dose and risk of hypoglycaemia were also similar in the two treatment groups. Weight gain was less with metformin plus biphasic insulin aspart 70/30 than with repaglinide plus biphasic insulin aspart 70/30 (difference in mean body weight between treatments −2.51 kg, 95% confidence interval −4.07 to −0.95).>Conclusions In non-obese patients with type 2 diabetes and poor glycaemic regulation on oral hypoglycaemic agents, overall glycaemic regulation with insulin in combination with metformin was equivalent to that with insulin plus repaglinide. Weight gain seemed less with insulin plus metformin than with insulin plus repaglinide.>Trial registration
机译:>目的研究胰岛素与二甲双胍或胰岛素促泌剂瑞格列奈联合治疗对非肥胖2型糖尿病患者血糖调节的影响。>设计盲人,双重假人,平行审判。 >设置丹麦于2003年至2006年之间的二级医疗服务。>参与者非肥胖患者(BMI≤27)且β细胞功能得以保留。 >干预在瑞格列奈联合二甲双胍联合治疗四个月后,糖化血红蛋白(HbA1c)浓度为6.5%或更高的患者被随机分配为瑞格列奈6 mg或二甲双胍2000 mg。所有患者还于晚餐前每天一次六个月一次接受双阶段门冬胰岛素70/30(30%可溶性门冬胰岛素和70%中间作用门冬胰岛素),共12个月。调整胰岛素剂量,以使空腹血糖浓度达到4.0-6.0 mmol / l。 HbA1c浓度的目标值低于6.5%。如果未达到血糖目标,则每天应加强治疗,注射2至3次胰岛素。>主要结果指标 HbA1c浓度。>结果在459名符合条件的患者中,有102名被随机分配,然后97完成了审判。患者患有2型糖尿病大约10年。在治疗结束时,两个治疗组中的HbA1c浓度降低了相似的量(胰岛素加二甲双胍:平均值(标准差)HbA1c 8.15%(1.32)v 6.72%(0.66);胰岛素加瑞格列奈:8.07%(1.49) )v 6.90%(0.68); P = 0.177)。在两个治疗组中,每日总胰岛素剂量和低血糖风险也相似。二甲双胍+天冬胰岛素+ 70/30的体重增加少于瑞格列奈+天冬胰岛素+ 70/30的体重增加(治疗之间的平均体重差异为-2.51 kg,95%置信区间为-4.07至-0.95)。>结论在非肥胖的2型糖尿病患者中,口服降糖药的血糖调节不良,胰岛素联合二甲双胍的总体血糖调节与胰岛素加瑞格列奈的总体血糖调节相同。胰岛素加二甲双胍的体重增加似乎少于胰岛素加瑞格列奈的体重增加。>试验注册

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