Department of Clinical Nutrition and Dietetics, Faculty of Nutrition and Food Technology, National Nutrition and Food Technology Research Institute, Shahid Beheshti University of Medical Sciences, No. 46, Arghavan-e-gharbi St., Farahzadi Blvd., Shahrak-e-qods, P.O.Box 19395-4741, Tehran, Iran.
Nutrition and Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, No. 24, Shahid Arabi St, Yemen Blvd, Chamran Exp, Tehran, Iran.
Eur J Nutr. 2021 Aug;60(5):2495-2506. doi: 10.1007/s00394-020-02419-6. Epub 2020 Nov 7.
This study aimed to investigate the effects of vitamin K supplementation in the form of menaquinone-7 (MK-7) on glucose, insulin, and lipid metabolism in patients with type 2 diabetes mellitus (T2DM).
In this double-blinded, placebo-controlled, randomized trial, 68 insulin-independent people with diabetes received either 180 µg MK-7 twice a day or placebo for 12 weeks. We assessed fasting plasma glucose (FPG) and insulin concentrations (primary outcomes), glycated hemoglobin (HbA1c), insulin sensitivity indices, and lipid profiles (secondary outcomes) at baseline and end of the trial.
At the end of the trial, FPG (effect size (ES) = - 0.68; p-adjusted = 0.031) and HbA1c (ES = - 0.36; p-adjusted = 0.004) were significantly lower in the vitamin K group compared with the placebo at the end of the trial. The number of participants achieved the target levels of glycemic control based on FPG, and HbA1c concentrations were significantly higher in the vitamin K group compared to the placebo group. Insulin concentrations (ES = - 0.29; p = 0.019) and homeostatic model assessment for insulin resistance (HOMA-IR) significantly decreased in the vitamin K group (ES = - 0.29; p = 0.019) compared to baseline, but their values were not significantly different compared to the placebo group at the end of the trial. No significant variation was observed in lipid profiles.
Daily intake of 360 µg Vitamin K in the form of MK-7 for 12-weeks reduces FPG and HbA1c in patients with T2DM but does not have a lipid-lowering effect.
本研究旨在探讨以甲萘醌-7(MK-7)形式补充维生素 K 对 2 型糖尿病(T2DM)患者葡萄糖、胰岛素和脂代谢的影响。
在这项双盲、安慰剂对照、随机试验中,68 名不依赖胰岛素的糖尿病患者每天服用 180μg MK-7 两次或安慰剂,共 12 周。我们在基线和试验结束时评估空腹血糖(FPG)和胰岛素浓度(主要结局)、糖化血红蛋白(HbA1c)、胰岛素敏感性指数和血脂谱(次要结局)。
试验结束时,与安慰剂组相比,维生素 K 组的 FPG(效应大小(ES)=-0.68;p 调整=0.031)和 HbA1c(ES=-0.36;p 调整=0.004)显著降低。根据 FPG 和 HbA1c 浓度达到血糖控制目标的参与者人数,维生素 K 组明显高于安慰剂组。维生素 K 组的胰岛素浓度(ES=-0.29;p=0.019)和稳态模型评估胰岛素抵抗(HOMA-IR)显著降低(ES=-0.29;p=0.019),但与安慰剂组相比,试验结束时其值无显著差异。血脂谱无明显变化。
每日摄入 360μg 以 MK-7 形式存在的维生素 K,持续 12 周,可降低 T2DM 患者的 FPG 和 HbA1c,但无降低血脂的作用。