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二肽基肽酶-4抑制剂吉格列汀在二甲双胍和磺脲类药物联合治疗血糖控制不佳的2型糖尿病患者中的疗效和安全性:一项为期24周的多中心、随机、双盲、安慰剂对照研究(TROICA研究)

Efficacy and safety of gemigliptin, a dipeptidyl peptidase-4 inhibitor, in patients with type 2 diabetes mellitus inadequately controlled with combination treatment of metformin and sulphonylurea: a 24-week, multicentre, randomized, double-blind, placebo-controlled study (TROICA study).

作者信息

Ahn Chang Ho, Han Kyung Ah, Yu Jae Myung, Nam Joo Young, Ahn Kyu Jeung, Oh Tae Keun, Lee Hyoung Woo, Lee Dae Ho, Kim Jaetaek, Chung Choon Hee, Park Tae Sun, Kim Byung Joon, Park Seok Won, Park Hyeong Kyu, Lee Kwang Jae, Kim Sang-Wook, Park Jeong Hyun, Ko Kwan Pyo, Kim Chong Hwa, Lee Hyunjin, Jang Hak Chul, Park Kyong Soo

机构信息

Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.

Department of Internal Medicine, Eulji General Hospital, Seoul, Korea.

出版信息

Diabetes Obes Metab. 2017 May;19(5):635-643. doi: 10.1111/dom.12866. Epub 2017 Feb 17.

Abstract

AIMS

To assess the efficacy and safety of gemigliptin, a dipeptidyl peptidase-4 inhibitor, added to metformin and sulphonylurea in patients with type 2 diabetes (T2DM).

MATERIALS AND METHODS

We conducted a randomized, double-blind, placebo-controlled trial in 219 Korean patients inadequately controlled with metformin and glimepiride. Participants were randomized to gemigliptin 50 mg once daily or placebo added to metformin and glimepiride. The primary endpoint was change in glycated haemoglobin (HbA1c) level from baseline to week 24.

RESULTS

The baseline HbA1c was 8.2% in both groups. The addition of gemigliptin to metformin and glimepiride significantly reduced HbA1c levels at week 24 compared with placebo (between-group difference in adjusted mean change -0.87%, 95% confidence interval [CI] -1.09% to -0.64%). Fasting plasma glucose level was also significantly reduced with gemigliptin (-0.93 mmol/L, 95% CI -1.50 to -0.35 mmol/L), and a higher proportion of participants achieved an HbA1c level of <7% (39.3% vs 5.5%; P <.001) in the gemigliptin group than in the placebo group. Total cholesterol and LDL cholesterol were modestly but significantly reduced in the gemigliptin group compared with the placebo group (-0.21 mmol/L, 95% CI -0.38 to -0.03 mmol/L for total cholesterol, -0.18 mmol/L, 95% CI -0.34 to -0.01 mmol/L for LDL cholesterol). The incidence of hypoglycaemia was 9.4% in the gemigliptin group and 2.7% in the placebo group.

CONCLUSIONS

Gemigliptin significantly improved glycaemic control in patients with T2DM inadequately controlled with metformin and sulphonylurea. The incidence of hypoglycaemia was higher with gemigliptin than with placebo, which highlights the importance of optimal dose adjustment for sulphonylurea.

摘要

目的

评估在二甲双胍和磺脲类药物基础上加用二肽基肽酶-4抑制剂吉格列汀对2型糖尿病(T2DM)患者的疗效和安全性。

材料与方法

我们对219例使用二甲双胍和格列美脲血糖控制不佳的韩国患者进行了一项随机、双盲、安慰剂对照试验。参与者被随机分为每日一次服用50毫克吉格列汀组或在二甲双胍和格列美脲基础上加用安慰剂组。主要终点是从基线到第24周糖化血红蛋白(HbA1c)水平的变化。

结果

两组的基线HbA1c均为8.2%。与安慰剂相比,在二甲双胍和格列美脲基础上加用吉格列汀在第24周时显著降低了HbA1c水平(调整后平均变化的组间差异为-0.87%,95%置信区间[CI]-1.09%至-0.64%)。吉格列汀也显著降低了空腹血糖水平(-0.93毫摩尔/升,95%CI-1.50至-0.35毫摩尔/升),并且吉格列汀组达到HbA1c水平<7%的参与者比例高于安慰剂组(39.3%对5.5%;P<.001)。与安慰剂组相比,吉格列汀组的总胆固醇和低密度脂蛋白胆固醇有适度但显著的降低(总胆固醇为-0.21毫摩尔/升,95%CI-0.38至-0.03毫摩尔/升;低密度脂蛋白胆固醇为-0.18毫摩尔/升,95%CI-0.34至-0.01毫摩尔/升)。低血糖发生率在吉格列汀组为9.4%,在安慰剂组为2.7%。

结论

吉格列汀显著改善了使用二甲双胍和磺脲类药物血糖控制不佳的T2DM患者的血糖控制。吉格列汀组的低血糖发生率高于安慰剂组,这突出了磺脲类药物最佳剂量调整的重要性。

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