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利拉鲁肽联合基础胰岛素与基础-餐时胰岛素治疗(BBIT)用于控制血糖、维持体重稳定和提高治疗满意度的比较:一项针对无严重胰岛素缺乏的 2 型糖尿病患者使用 BBIT 治疗的随机前瞻性试点研究。

Comparison of liraglutide plus basal insulin and basal-bolus insulin therapy (BBIT) for glycemic control, body weight stability, and treatment satisfaction in patients treated using BBIT for type 2 diabetes without severe insulin deficiency: A randomized prospective pilot study.

机构信息

Department of Medicine, Division of Diabetes, Metabolism, and Endocrinology, Showa University School of Medicine, Japan.

Department of Medicine, Division of Diabetes, Metabolism, and Endocrinology, Showa University School of Medicine, Japan.

出版信息

Diabetes Res Clin Pract. 2018 Jun;140:339-346. doi: 10.1016/j.diabres.2018.03.032. Epub 2018 Mar 26.

DOI:10.1016/j.diabres.2018.03.032
PMID:29588170
Abstract

AIMS

We examined whether 0.9 mg/day liraglutide plus basal insulin (Lira-basal) is superior to basal-bolus insulin therapy (BBIT) for type 2 diabetes (T2DM) without severe insulin deficiency as determined by glucagon stimulation.

METHODS

Fifty patients receiving BBIT were enrolled in this 24-week, prospective, randomized, open-labeled study. After excluding subjects with fasting C-peptide immunoreactivity (CPR) < 1.0 ng/mL and CPR increase < 1.0 ng/mL at 6 min post glucagon injection, 25 were randomly allocated to receive Lira-basal (n = 12) or continued BBIT (n = 13). Primary endpoint was change in HbA1c. Secondary endpoints were changes in body weight (BW), 7-point self-monitored blood glucose (SMBG), and Diabetes Treatment Satisfaction Questionnaire status (DTSQs) scores.

RESULT

The Lira-basal group demonstrated reduced HbA1c, whereas the BBIT group showed no change. BW was reduced in the Lira-basal group but increased in the BBIT group. The Lira-basal group also exhibited significantly reduced pre-breakfast and pre-lunch SMBG. DTSQs scores improved in the Lira-basal group but not the BBIT group. Plasma lipids, liver function, and kidney function were not significantly changed in either group.

CONCLUSIONS

Lira-basal therapy is superior to BBIT for T2DM without severe insulin deficiency. This study was registered with UMIN Clinical Trials Registry (UMIN000028313).

摘要

目的

我们研究了在不伴有严重胰岛素缺乏的情况下(通过胰高血糖素刺激确定),每天 0.9mg 利拉鲁肽联合基础胰岛素(利拉基础)是否优于基础-餐时胰岛素治疗(BBIT)。

方法

本 24 周前瞻性随机开放标签研究纳入了 50 名接受 BBIT 的 2 型糖尿病(T2DM)患者。排除空腹 C 肽免疫活性(CPR)<1.0ng/mL 和胰高血糖素刺激后 6 分钟 CPR 增加<1.0ng/mL 的患者后,将 25 名患者随机分为利拉基础组(n=12)或继续 BBIT 组(n=13)。主要终点是 HbA1c 的变化。次要终点是体重(BW)、7 点自我监测血糖(SMBG)和糖尿病治疗满意度问卷(DTSQs)评分的变化。

结果

利拉基础组的 HbA1c 降低,而 BBIT 组没有变化。利拉基础组 BW 降低,BBIT 组 BW 增加。利拉基础组早餐前和午餐前 SMBG 也显著降低。利拉基础组 DTSQs 评分改善,但 BBIT 组没有。两组血脂、肝功能和肾功能均无明显变化。

结论

对于不伴有严重胰岛素缺乏的 T2DM,利拉基础治疗优于 BBIT。本研究在日本临床试验注册中心(UMIN000028313)注册。

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