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The effect of initial therapy with the fixed-dose combination of sitagliptin and metformin compared with metformin monotherapy in patients with type 2 diabetes mellitus.

机译:西他列汀和二甲双胍固定剂量联合初始治疗与二甲双胍单药治疗相比在2型糖尿病患者中的效果。

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AIMS: This study was conducted to compare the glycaemic efficacy and safety of initial combination therapy with the fixed-dose combination of sitagliptin and metformin versus metformin monotherapy in drug-naive patients with type 2 diabetes. METHODS: This double-blind study (18-week Phase A and 26-week Phase B) randomized 1250 drug-naIve patients with type 2 diabetes [mean baseline haemoglobin A1c (HbA1c) 9.9%] to sitagliptin/metformin 50/500 mg bid or metformin 500 mg bid (uptitrated over 4 weeks to achieve maximum doses of sitagliptin/metformin 50/1000 mg bid or metformin 1000 bid). Results of the primary efficacy endpoint (mean HbA1c reductions from baseline at the end of Phase A) are reported herein. RESULTS: At week 18, mean change from baseline HbA1c was -2.4% for sitagliptin/metformin FDC and -1.8% for metformin monotherapy (p < 0.001); more patients treated with sitagliptin/metformin FDC had an HbA1c value <7% (p < 0.001) versus metformin monotherapy. Changes in fasting plasma glucose were significantly greater with sitagliptin/metformin FDC (-3.8 mmol/l) versus metformin monotherapy (-3.0 mmol/l; p < 0.001). Homeostasis model assessment of beta-cell function (HOMA-beta) and fasting proinsulin/insulin ratio were significantly improved with sitagliptin/metformin FDC versus metformin monotherapy. Baseline body weight was reduced by 1.6 kg in each group. Both treatments were generally well tolerated with a low and similar incidence of hypoglycaemia. Abdominal pain (1.1 and 3.9%; p = 0.002) and diarrhoea (12.0 and 16.6%; p = 0.021) occurred significantly less with sitagliptin/metformin FDC versus metformin monotherapy; the incidence of nausea and vomiting was similar in both groups. CONCLUSION: Compared with metformin monotherapy, initial treatment with sitagliptin/metformin FDC provided superior glycaemic improvement with a similar degree of weight loss and lower incidences of abdominal pain and diarrhoea.
机译:目的:本研究旨在比较初治联合西他列汀和二甲双胍固定剂量联合单药联合二甲双胍治疗初治2型糖尿病患者的血糖有效性和安全性。方法:这项双盲研究(A期18周和B期26周)将1250例2型糖尿病初治患者[平均基线血红蛋白A1c(HbA1c)9.9%]随机分配至西他列汀/二甲双胍50/500 mg bid或二甲双胍500 mg bid(经过4周的调整以达到西他列汀/二甲双胍50/1000 mg bid或二甲双胍1000 bid的最大剂量)。本文报道了主要功效终点的结果(平均Ab期HbA1c从基线降低)。结果:在第18周,西他列汀/二甲双胍FDC与基线HbA1c的平均变化为-2.4%,二甲双胍单药为-1.8%(p <0.001);与二甲双胍单药治疗相比,更多接受西他列汀/二甲双胍FDC治疗的患者HbA1c值<7%(p <0.001)。西他列汀/二甲双胍FDC(-3.8 mmol / l)与二甲双胍单药治疗(-3.0 mmol / l; p <0.001)相比,空腹血糖变化明显更大。西他列汀/二甲双胍FDC与二甲双胍单药治疗相比,β细胞功能(HOMA-beta)和空腹胰岛素/胰岛素比率的稳态模型评估显着改善。每组的基线体重减少了1.6公斤。两种疗法一般都具有良好的耐受性,低血糖发生率低且相似。西他列汀/二甲双胍FDC与二甲双胍单药治疗相比,腹痛(1.1和3.9%; p = 0.002)和腹泻(12.0和16.6%; p = 0.021)的发生率明显降低。两组的恶心和呕吐发生率相似。结论:与二甲双胍单药治疗相比,西他列汀/二甲双胍FDC的初始治疗可改善血糖,减轻体重,腹部疼痛和腹泻的发生率也较低。

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