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加用沙格列汀与增加二甲双胍剂量。

Adding saxagliptin to extended-release metformin vs. uptitrating metformin dosage.

机构信息

Department of Medicine, Tulane University Health Sciences Center, 1430 Tulane Avenue, New Orleans, LA 70112, USA.

出版信息

Diabetes Obes Metab. 2012 Apr;14(4):365-71. doi: 10.1111/j.1463-1326.2011.01553.x. Epub 2012 Jan 18.

Abstract

AIM

To investigate whether patients taking metformin for type 2 diabetes mellitus (T2DM) have improved glycaemic control without compromising tolerability by adding an agent with a complementary mechanism of action vs. uptitrating metformin.

METHODS

Adults with T2DM and glycated haemoglobin (HbA1c) between 7.0 and 10.5% receiving metformin extended release (XR) 1500 mg/day for ≥8 weeks were randomized to receive saxagliptin 5 mg added to metformin XR 1500 mg (n = 138) or metformin XR uptitrated to 2000 mg/day (n = 144). Endpoints were change from baseline to week 18 in HbA1c (primary), 120-min postprandial glucose (PPG), fasting plasma glucose (FPG) and the proportion of patients achieving HbA1c <7%.

RESULTS

At week 18, the adjusted mean reduction from baseline HbA1c was -0.88% for saxagliptin + metformin XR and -0.35% for uptitrated metformin XR (difference, -0.52%; p < 0.0001). For 120-min PPG and FPG, differences in adjusted mean change from baseline between saxagliptin + metformin XR and uptitrated metformin XR were -1.3 mmol/l (-23.32 mg/dl) (p = 0.0013) and -0.73 mmol/l (-13.18 mg/dl) (p = 0.0030), respectively. More patients achieved HbA1c <7.0% with saxagliptin + metformin XR than with uptitrated metformin XR (37.2 vs. 26.1%; p = 0.0459). The proportions of patients experiencing any adverse events (AEs) were generally similar between groups; neither group showed any notable difference in hypoglycaemia or gastrointestinal AEs.

CONCLUSION

Adding saxagliptin to metformin XR provided superior glycaemic control compared with uptitrating metformin XR without the emergence of additional safety concerns.

摘要

目的

研究对于接受二甲双胍治疗的 2 型糖尿病(T2DM)患者,加用作用机制互补的药物而不是增加二甲双胍剂量,是否可在不降低耐受性的情况下改善血糖控制。

方法

接受二甲双胍缓释片(XR)1500mg/天治疗≥8 周,糖化血红蛋白(HbA1c)在 7.0%至 10.5%之间的 T2DM 成人患者,随机分为加用沙格列汀 5mg 联合二甲双胍 XR 1500mg(n=138)或增加二甲双胍 XR 剂量至 2000mg/天(n=144)。主要终点为治疗 18 周时与基线相比的 HbA1c 变化(首要终点)、120 分钟餐后血糖(PPG)、空腹血糖(FPG)以及达到 HbA1c<7%的患者比例。

结果

治疗 18 周时,沙格列汀+二甲双胍 XR 组与增加剂量的二甲双胍 XR 组的 HbA1c 自基线的平均降幅分别为-0.88%和-0.35%(差值,-0.52%;p<0.0001)。对于 120 分钟 PPG 和 FPG,沙格列汀+二甲双胍 XR 与增加剂量的二甲双胍 XR 组的调整后平均变化差值分别为-1.3mmol/L(-23.32mg/dl)(p=0.0013)和-0.73mmol/L(-13.18mg/dl)(p=0.0030)。沙格列汀+二甲双胍 XR 组较增加剂量的二甲双胍 XR 组达到 HbA1c<7.0%的患者比例更高(37.2%比 26.1%;p=0.0459)。两组患者的不良事件(AE)总发生率相当,两组间均无明显差异的低血糖或胃肠道 AE。

结论

与增加二甲双胍 XR 剂量相比,加用沙格列汀可提供更好的血糖控制,且无额外的安全性担忧。

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