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对于基础胰岛素控制不佳的 2 型糖尿病患者,加用每日一次的利西那肽:一项 24 周、随机、安慰剂对照比较研究(GetGoal-L)。

Adding once-daily lixisenatide for type 2 diabetes inadequately controlled by established basal insulin: a 24-week, randomized, placebo-controlled comparison (GetGoal-L).

机构信息

Oregon Health & Science University, Portland, Oregon, USA.

出版信息

Diabetes Care. 2013 Sep;36(9):2489-96. doi: 10.2337/dc12-2454. Epub 2013 Apr 29.

Abstract

OBJECTIVE

To examine the efficacy and safety of adding the once-daily glucagon-like peptide-1 receptor agonist (GLP-1RA) lixisenatide to established basal insulin therapy alone or together with metformin, in people with type 2 diabetes and elevated glycated hemoglobin (HbA1c).

RESEARCH DESIGN AND METHODS

We conducted a double-blind, parallel-group, placebo-controlled trial. Patients (n = 495) with established basal insulin therapy but inadequate glycemic control were randomized to add lixisenatide 20 μg or placebo for 24 weeks. Basal insulin dosage was unchanged except to limit hypoglycemia. HbA1c reduction from baseline was the primary end point.

RESULTS

Mean duration of diabetes was 12.5 years, duration of insulin use was 3.1 years, insulin dosage was 55 units/day, and baseline HbA1c was 8.4%. With lixisenatide, the placebo-corrected change of HbA1c from baseline was -0.4% (95% CI -0.6 to -0.2; P = 0.0002), and mean HbA1c at end point was 7.8%. HbA1c <7.0% (53 mmol/mol) was attained by more lixisenatide (28%) than placebo (12%; P < 0.0001) participants. Lixisenatide reduced plasma glucose levels after a standardized breakfast (placebo-corrected reduction, -3.8 mmol/L; P < 0.0001); seven-point glucose profiles showed a reduction persisting through the day. Reductions in body weight (placebo corrected, -1.3 kg; P < 0.0001) and insulin dosage (-3.7 units/day; P = 0.012) were greater with lixisenatide. Main adverse events (AEs) with lixisenatide were gastrointestinal. Symptomatic hypoglycemia was 28% for lixisenatide and 22% for placebo; 4 of 328 subjects (1.2%) had severe hypoglycemia with lixisenatide vs. 0 of 167 with placebo.

CONCLUSIONS

By improving HbA1c and postprandial hyperglycemia without weight gain in type 2 diabetes with inadequate glycemic control despite stable basal insulin, lixisenatide may provide an alternative to rapid-acting insulin or other treatment options.

摘要

目的

评估每日一次胰高血糖素样肽-1 受体激动剂(GLP-1RA)利西那肽联合或不联合二甲双胍添加至已接受基础胰岛素治疗的 2 型糖尿病患者中的疗效和安全性,这些患者糖化血红蛋白(HbA1c)升高。

研究设计和方法

我们进行了一项双盲、平行组、安慰剂对照试验。495 名接受基础胰岛素治疗但血糖控制不佳的患者被随机分为加用利西那肽 20μg 或安慰剂组,治疗 24 周。除了限制低血糖外,基础胰岛素剂量保持不变。从基线的 HbA1c 降低是主要终点。

结果

平均糖尿病病程为 12.5 年,胰岛素使用时间为 3.1 年,胰岛素剂量为 55 单位/天,基线 HbA1c 为 8.4%。利西那肽治疗组与安慰剂组相比,HbA1c 从基线的校正变化为-0.4%(95%CI -0.6 至 -0.2;P=0.0002),终点时的平均 HbA1c 为 7.8%。更多的利西那肽(28%)而非安慰剂(12%)患者达到了 HbA1c<7.0%(53mmol/mol)(P<0.0001)。利西那肽降低了早餐后(安慰剂校正,-3.8mmol/L;P<0.0001)的血糖水平;七点血糖谱显示全天持续降低。体重(安慰剂校正,-1.3kg;P<0.0001)和胰岛素剂量(-3.7 单位/天;P=0.012)的降低也更大。利西那肽的主要不良事件(AE)为胃肠道事件。利西那肽组发生低血糖症状的患者为 28%,安慰剂组为 22%;利西那肽组有 4 例(1.2%)严重低血糖,安慰剂组无 0 例。

结论

在血糖控制不佳的 2 型糖尿病患者中,尽管基础胰岛素稳定,但利西那肽仍可改善 HbA1c 和餐后高血糖,且不增加体重,为速效胰岛素或其他治疗选择提供了替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fc7/3747925/8f80064973f1/2489fig1.jpg

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