Adelaide Medical School and Centre of Research Excellence in Translating Nutritional Science to Good Health, The University of Adelaide, Adelaide, Australia.
Endocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, Australia.
Diabetologia. 2024 Jul;67(7):1260-1270. doi: 10.1007/s00125-024-06131-6. Epub 2024 Apr 1.
AIMS/HYPOTHESIS: Metformin lowers postprandial glycaemic excursions in individuals with type 2 diabetes by modulating gastrointestinal function, including the stimulation of glucagon-like peptide-1 (GLP-1). The impact of varying the timing of metformin administration on postprandial glucose metabolism is poorly defined. We evaluated the effects of metformin, administered at different intervals before an intraduodenal glucose infusion, on the subsequent glycaemic, insulinaemic and GLP-1 responses in metformin-treated type 2 diabetes.
Sixteen participants with type 2 diabetes that was relatively well-controlled by metformin monotherapy were studied on four separate days in a crossover design. On each day, participants were randomised to receive a bolus infusion of metformin (1000 mg in 50 ml 0.9% saline) via a nasoduodenal catheter at t = -60, -30 or 0 min (and saline at the other timepoints) or saline at all timepoints (control), followed by an intraduodenal glucose infusion of 12.56 kJ/min (3 kcal/min) at t = 0-60 min. The treatments were blinded to both participants and investigators involved in the study procedures. Plasma glucose, insulin and total GLP-1 levels were measured every 30 min between t = -60 min and t = 120 min.
There was a treatment-by-time interaction for metformin in reducing plasma glucose levels and increasing plasma GLP-1 and insulin levels (p<0.05 for each). The reduction in plasma glucose levels was greater when metformin was administered at t = -60 or -30 min vs t = 0 min (p<0.05 for each), and the increases in plasma GLP-1 levels were evident only when metformin was administered at t = -60 or -30 min (p<0.05 for each). Although metformin did not influence insulin sensitivity, it enhanced glucose-induced insulin secretion (p<0.05), and the increases in plasma insulin levels were comparable on the 3 days when metformin was given.
CONCLUSIONS/INTERPRETATION: In well-controlled metformin-treated type 2 diabetes, glucose-lowering by metformin is greater when it is given before, rather than with, enteral glucose, and this is associated with a greater GLP-1 response. These observations suggest that administration of metformin before meals may optimise its effect in improving postprandial glycaemic control.
www.anzctr.org.au ACTRN12621000878875 FUNDING: The study was not funded by a specific research grant.
目的/假设:二甲双胍通过调节胃肠道功能(包括刺激胰高血糖素样肽-1(GLP-1))降低 2 型糖尿病患者餐后血糖波动。二甲双胍给药时间的变化对餐后血糖代谢的影响尚未明确。我们评估了在十二指肠内葡萄糖输注前不同时间给予二甲双胍对二甲双胍治疗的 2 型糖尿病患者随后的血糖、胰岛素和 GLP-1 反应的影响。
在一项交叉设计中,在 4 天内在 16 名血糖控制相对较好的 2 型糖尿病患者中进行了研究。在每一天,参与者随机接受通过鼻十二指肠管在 t = -60、-30 或 0 分钟(在其他时间点给予生理盐水)或所有时间点给予生理盐水(对照)的二甲双胍(1000 毫克在 50 毫升 0.9%生理盐水中)的推注,随后在 t = 0-60 分钟时进行 12.56 kJ/min(3 kcal/min)的十二指肠内葡萄糖输注。两种治疗方案均对参与研究程序的参与者和研究人员均设盲。在 t = -60 分钟至 t = 120 分钟之间,每 30 分钟测量一次血浆葡萄糖、胰岛素和总 GLP-1 水平。
二甲双胍在降低血糖水平和增加血浆 GLP-1 和胰岛素水平方面存在治疗与时间的相互作用(p<0.05)。与 t = 0 分钟相比,在 t = -60 或 -30 分钟给予二甲双胍时血糖水平降低更大(p<0.05),并且仅在 t = -60 或 -30 分钟给予二甲双胍时才出现血浆 GLP-1 水平的升高(p<0.05)。尽管二甲双胍不影响胰岛素敏感性,但它增强了葡萄糖诱导的胰岛素分泌(p<0.05),并且当在 3 天内给予二甲双胍时,血浆胰岛素水平的增加相当。
结论/解释:在血糖控制良好的二甲双胍治疗的 2 型糖尿病患者中,在给予肠内葡萄糖之前给予二甲双胍可更大程度地降低血糖,并且与更大的 GLP-1 反应相关。这些观察结果表明,餐前给予二甲双胍可能会优化其改善餐后血糖控制的效果。
www.anzctr.org.au ACTRN12621000878875 资金来源:该研究未获得特定研究基金的资助。