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米格列醇和二甲双胍联合治疗对 2 型糖尿病患者血糖控制的影响。

Effect of the combination of mitiglinide and metformin on glycemic control in patients with type 2 diabetes mellitus.

机构信息

Department of Internal Medicine, Seoul National University College of Medicine.

Department of Internal Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea.

出版信息

J Diabetes Investig. 2010 Aug 2;1(4):143-8. doi: 10.1111/j.2040-1124.2010.00023.x.

Abstract

UNLABELLED

Aims/Introduction:  Mitiglinide is the newest drug in the meglitinide family. It increases the early-phase insulin release through rapid association-dissociation kinetics in the pancreatic β cells. The efficacy and safety of adding meglitinide to metformin monotherapy in patients with type 2 diabetes are unknown.

MATERIALS AND METHODS

We carried out a prospective, randomized, multicenter trial to assess the efficacy and safety of combined treatment with mitiglinide and metformin for patients with type 2 diabetes who showed inadequate glycemic control with metformin monotherapy. Subjects with glycated hemoglobin (HbA1c) >7.0% after an 8-week metformin run-in phase were randomized to a 16-week trial phase with metformin plus mitiglinide (Met + Mit) or metformin plus placebo (Met + Pcb).

RESULTS

Compared with the Met + Pcb group, the Met + Mit group showed a greater reduction in HbA1c (-0.7 ± 0.6%vs-0.4 ± 0.7%, P = 0.002), fasting plasma glucose (-0.77 ± 1.76 mmol/L vs-0.05 ± 1.60 mmol/L, P = 0.015) and 2-h postprandial glucose (-3.76 ± 3.57 mmol/L vs-0.84 ± 3.07 mmol/L, P < 0.0001). The proportion of the patients who achieved the target HbA1c value of <7% at the end of the study was also higher in the Met + Mit group than the Met + Pcb group (49.3%vs 28.8%, P = 0.016). There were no differences in the adverse event rates between groups.

CONCLUSIONS

Combination therapy with metformin and mitiglinide is effective and safe for the treatment of patients with type 2 diabetes who have inadequate glycemic control with metformin monotherapy. (J Diabetes Invest, doi: 10.1111/j.2040-1124.2010.00023.x, 2010).

摘要

目的/引言:米格列醇是新型的二肽基肽酶-4(DPP-4)抑制剂,通过快速的胰腺β细胞结合-解离动力学,增加早期胰岛素释放。在二甲双胍单药治疗的 2 型糖尿病患者中,联合应用米格列醇治疗的疗效和安全性尚不清楚。

材料和方法

我们进行了一项前瞻性、随机、多中心试验,以评估米格列醇联合二甲双胍治疗血糖控制不佳的 2 型糖尿病患者的疗效和安全性。在 8 周的二甲双胍导入期后,糖化血红蛋白(HbA1c)>7.0%的患者被随机分为 16 周的试验期,接受二甲双胍加米格列醇(Met+Mit)或二甲双胍加安慰剂(Met+PCb)治疗。

结果

与 Met+PCb 组相比,Met+Mit 组 HbA1c 降低更明显(-0.7±0.6%比-0.4±0.7%,P=0.002),空腹血糖(-0.77±1.76mmol/L 比-0.05±1.60mmol/L,P=0.015)和餐后 2 小时血糖(-3.76±3.57mmol/L 比-0.84±3.07mmol/L,P<0.0001)降低更明显。研究结束时,Met+Mit 组达到 HbA1c 目标值<7%的患者比例也高于 Met+PCb 组(49.3%比 28.8%,P=0.016)。两组不良反应发生率无差异。

结论

对于血糖控制不佳的二甲双胍单药治疗的 2 型糖尿病患者,联合应用二甲双胍和米格列醇治疗是有效和安全的。(J Diabetes Invest, doi: 10.1111/j.2040-1124.2010.00023.x, 2010)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fd0/4008006/00bebe4ef238/jdi-1-143-g1.jpg

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