Faculty of Medicine, Zagazig University, Zagazig, Egypt; Zagazig Medical Research Society (ZMRS), Zagazig, Egypt.
Faculty of Medicine, Zagazig University, Zagazig, Egypt; Zagazig Medical Research Society (ZMRS), Zagazig, Egypt.
Diabetes Metab Syndr. 2021 Nov-Dec;15(6):102323. doi: 10.1016/j.dsx.2021.102323. Epub 2021 Oct 28.
Imeglimin is a novel tetrahydrotriazine-containing drug suggested as a safe drug for glycemic management in patients with type 2 diabetes mellitus (T2DM). We aimed to 1) evaluate the efficacy of imeglimin on glycemic control and insulin resistance improvement measured by homeostatic model assessment of insulin resistance (HOMA-IR). 2) assess whether the novel drug improves lipid parameters in diabetic patients. 3) compare between different doses regarding safety.
We searched PubMed, Cochrane Library, Scopus, Web of Science, Google Scholar, and Wiley through April 25, 2021, for relevant randomized controlled trials comparing different doses of imeglimin supplied as a monotherapy or as add-on therapy versus placebo for adult patients with type 2 diabetes mellitus. Data on glycemic and lipid parameters and adverse events were extracted and pooled in random-effect models using Review Manager version 5.3.
Eight studies comprising 1555 patients with T2DM were included in this study. The overall effect estimate of the meta-analysis showed that the imeglimin group was superior to the control group concerning glycated hemoglobin and fasting plasma glucose (P < 0.00001). However, it did not affect HOMA-IR or lipid parameters, including triglyceride, LDL-C, and HDL-C (all p > 0.05). Regarding safety profile, imeglimin was safe and tolerable with no treatment-emergent or serious adverse events.
Imeglimin safely improved glycemic control by reducing HbA1c and FPG. However, no beneficial effects regarding insulin resistance measured by HOMA-IR or lipid parameters were observed. Further high-quality RCTs with high dose imeglimin are encouraged to ensure HOMA-IR and lipid parameters results.
依格列净是一种新型的四氢三嗪类药物,被认为是治疗 2 型糖尿病(T2DM)患者血糖控制的安全药物。我们旨在:1)评估依格列净对血糖控制和胰岛素抵抗改善的疗效,通过稳态模型评估的胰岛素抵抗(HOMA-IR)来衡量。2)评估新型药物是否改善糖尿病患者的血脂参数。3)比较不同剂量之间的安全性。
我们通过 4 月 25 日之前的 PubMed、Cochrane 图书馆、Scopus、Web of Science、Google Scholar 和 Wiley 搜索了相关的随机对照试验,比较了不同剂量的依格列净作为单一疗法或联合疗法与安慰剂治疗成人 2 型糖尿病患者的效果。使用 Review Manager 版本 5.3 提取并汇总了血糖和血脂参数以及不良反应的数据,并采用随机效应模型进行分析。
本研究共纳入了 8 项研究,涉及 1555 例 T2DM 患者。荟萃分析的总体效果估计表明,依格列净组在糖化血红蛋白和空腹血糖方面优于对照组(P<0.00001)。然而,它对 HOMA-IR 或血脂参数(包括甘油三酯、LDL-C 和 HDL-C)没有影响(均 P>0.05)。关于安全性概况,依格列净是安全且可耐受的,没有治疗相关的不良事件或严重不良事件。
依格列净通过降低 HbA1c 和 FPG 安全地改善了血糖控制。然而,在 HOMA-IR 或血脂参数方面没有观察到有益的效果。鼓励进行更多高质量的 RCT 研究,以确定依格列净的高剂量是否会对 HOMA-IR 和血脂参数产生影响。