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利西那肽对比磺脲类药物联合基础胰岛素治疗用于选择在斋月期间禁食的 2 型糖尿病患者(LixiRam)的安全性:一项国际、随机、开放标签试验。

Safety of lixisenatide versus sulfonylurea added to basal insulin treatment in people with type 2 diabetes mellitus who elect to fast during Ramadan (LixiRam): An international, randomized, open-label trial.

机构信息

Dubai Hospital, Dubai, United Arab Emirates.

Osmania Medical College, Hyderabad, India.

出版信息

Diabetes Res Clin Pract. 2019 Apr;150:331-341. doi: 10.1016/j.diabres.2019.01.035. Epub 2019 Feb 14.

DOI:10.1016/j.diabres.2019.01.035
PMID:30772385
Abstract

AIMS

Adding lixisenatide to basal insulin (BI) instead of sulfonylurea (SU), versus continuing SU + BI was assessed in people with type 2 diabetes mellitus (T2DM) who intended to fast during Ramadan 2017.

METHODS

LixiRam (NCT02941367) was a phase 4, randomized, open-label, 12-22-week study in people with T2DM insufficiently controlled with SU + BI ± 1 oral anti-diabetic. Endpoints included the percentage of participants with ≥1 documented symptomatic hypoglycemia event (plasma glucose ≤70 mg/dL; primary endpoint) and any hypoglycemia during Ramadan fasting.

RESULTS

A numerically lower percentage of participants with lixisenatide + BI (3.3%, 3/91) versus SU + BI (8.9%, 8/90) had ≥1 documented symptomatic hypoglycemia event (intent-to-treat visit 4) during Ramadan fasting (OR: 0.34; 95% CI 0.09, 1.35; proportion difference -0.06, 95% CI -0.13, 0.01); the difference was statistically significant for the 'any hypoglycemia' category (lixisenatide + BI: 4.3%, 4/92; SU + BI: 17.4%, 16/92; OR: 0.22; 95% CI 0.07, 0.68; proportion difference -0.13, 95% CI -0.22, -0.04; intent-to-treat). No new treatment-emergent adverse events occurred.

CONCLUSIONS

Compared with SU + BI, lixisenatide + BI provided lower rates of any hypoglycemia in people with T2DM during Ramadan fasting. Lixisenatide + BI therapy may be a suitable treatment option during fasting.

摘要

目的

在 2017 年打算在斋月期间禁食的 2 型糖尿病(T2DM)患者中,评估与继续使用磺酰脲类药物(SU)+基础胰岛素(BI)相比,将利西那肽加入基础胰岛素(BI)治疗是否可以改善血糖控制。

方法

LixiRam(NCT02941367)是一项 2 型糖尿病患者的 4 期、随机、开放标签、12-22 周的研究,这些患者使用 SU+BI+/-1 种口服抗糖尿病药物治疗血糖仍控制不佳。主要终点包括≥1 例有记录的症状性低血糖事件(血糖≤70mg/dL)的患者比例(主要终点)和在斋月禁食期间的任何低血糖事件。

结果

在斋月禁食期间(意向治疗访视 4),接受利西那肽+BI 治疗的患者中(3.3%,3/91)与接受 SU+BI 治疗的患者(8.9%,8/90)有≥1 例有记录的症状性低血糖事件的患者比例更低(OR:0.34;95%CI 0.09,1.35;比例差异-0.06,95%CI-0.13,0.01);在“任何低血糖”类别中,差异具有统计学意义(利西那肽+BI:4.3%,4/92;SU+BI:17.4%,16/92;OR:0.22;95%CI 0.07,0.68;比例差异-0.13,95%CI-0.22,-0.04);在接受意向治疗的患者中,没有发生新的治疗中出现的不良事件。

结论

与 SU+BI 相比,在 T2DM 患者进行斋月禁食期间,利西那肽+BI 治疗可降低低血糖的发生率。在禁食期间,利西那肽+BI 治疗可能是一种合适的治疗选择。

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