Orange County Research Center, 14351 Myford Rd, Suite B, Tustin, CA, 93780, USA,
Diabetes Ther. 2013 Dec;4(2):269-83. doi: 10.1007/s13300-013-0028-9. Epub 2013 Jul 24.
Saxagliptin added to metformin extended release (XR) and uptitrated metformin XR were evaluated for their impact on daily glucose measurements and their tolerability in patients with type 2 diabetes mellitus (T2DM) inadequately controlled with metformin monotherapy.
Patients aged 18-78 years on metformin 850-1,500 mg with glycated hemoglobin (HbA1c) 7.5-11.5% at screening were eligible for this double-blind, active-controlled study. Patients were stabilized on metformin XR 1,500 mg before randomization. Patients with HbA1c 7-11% and fasting plasma glucose (FPG) ≥126 mg/dL after a 4- 8-week lead-in period were randomly assigned to saxagliptin 5 mg + metformin XR 1,500 mg or metformin XR 500 mg + metformin XR 1,500 mg (uptitrated metformin XR). The primary end point was change from baseline to week 4 in 24-h mean weighted glucose (MWG). Secondary end points were changes from baseline to week 4 in 2-h postprandial glucose (PPG) and FPG.
At week 4, the adjusted mean ± SE change from baseline in 24-h MWG was -19.0 ± 5.7 mg/dL (95% CI -30.3 to -7.6) for saxagliptin + metformin XR and -8.2 ± 6.0 mg/dL (95% CI -20.0 to 3.7) for uptitrated metformin XR. Mean changes from baseline in 2-h PPG and FPG were numerically greater with saxagliptin + metformin XR versus uptitrated metformin XR. The incidence of adverse events was lower with saxagliptin + metformin XR (17.4%) versus uptitrated metformin XR (31.9%) mainly due to differences in gastrointestinal adverse event incidence (2.2% vs 10.6%, respectively). There were no reports of confirmed hypoglycemia in either group.
In this 4-week study in patients with T2DM inadequately controlled with metformin monotherapy, saxagliptin added to metformin XR demonstrated a trend for improvement in measures of daily glycemic control, with fewer gastrointestinal adverse events, compared with uptitrated metformin.
在二甲双胍单药治疗控制不佳的 2 型糖尿病(T2DM)患者中,评估将沙格列汀添加至二甲双胍缓释片(XR)并逐渐增加二甲双胍 XR 剂量对日常血糖测量的影响及其耐受性。
在筛选时接受二甲双胍 850-1500mg 治疗且糖化血红蛋白(HbA1c)为 7.5-11.5%的年龄为 18-78 岁的患者有资格参加这项双盲、活性对照研究。在随机分组前,患者接受二甲双胍 XR 1500mg 稳定治疗。在 4-8 周导入期后,HbA1c 为 7-11%且空腹血糖(FPG)≥126mg/dL 的患者随机分配至沙格列汀 5mg+二甲双胍 XR 1500mg 或二甲双胍 XR 500mg+二甲双胍 XR 1500mg(逐渐增加的二甲双胍 XR)组。主要终点是从基线到第 4 周时 24 小时平均加权血糖(MWG)的变化。次要终点是从基线到第 4 周时 2 小时餐后血糖(PPG)和 FPG 的变化。
第 4 周时,沙格列汀+二甲双胍 XR 组从基线的调整均值±SE 变化为-19.0±5.7mg/dL(95%CI-30.3 至-7.6),逐渐增加的二甲双胍 XR 组为-8.2±6.0mg/dL(95%CI-20.0 至 3.7)。与逐渐增加的二甲双胍 XR 相比,沙格列汀+二甲双胍 XR 组的 2 小时 PPG 和 FPG 均值变化从基线开始时数值更大。沙格列汀+二甲双胍 XR 组(17.4%)的不良事件发生率低于逐渐增加的二甲双胍 XR 组(31.9%),主要是由于胃肠道不良事件发生率的差异(分别为 2.2%和 10.6%)。两组均无确诊低血糖的报告。
在这项为期 4 周的研究中,在二甲双胍单药治疗控制不佳的 T2DM 患者中,与逐渐增加的二甲双胍 XR 相比,沙格列汀添加至二甲双胍 XR 可改善日常血糖控制的测量指标,胃肠道不良事件更少。