Department of Endocrinology, Wolfson Med Center, Holon, Israel.
Cardiovasc Diabetol. 2012 Jun 7;11:61. doi: 10.1186/1475-2840-11-61.
Insulin resistance (IR) is the major driving force behind development and progression of atherosclerosis in patients with nonalcoholic fatty liver disease (NAFLD). Therefore, correction of IR is a relevant therapeutic target.We performed the current trial to evaluate whether 12- month metformin therapy improves vascular stiffness in patients with NAFLD and to assess if this improvement is associated with change in glucose control, insulin resistance or circulating adiponectin.
In randomized, placebo controlled study, 63 patients with NAFLD were assigned to one of two groups: Group 1 received daily metformin; Group 2 received placebo. Central aortic augmentation index (AI) was performed using SphygmoCor (version 7.1, AtCor Medical, Sydney, Australia) at baseline, at 4-and 12-month treatment period. Metabolic parameters, insulin resistance markers and serum adiponectin levels were determined.
In placebo group: AI did not improve during the treatment period. Liver function and adiponectin levels did not change during the study.In multiple linear regression analysis, the independent predictors of arterial stiffness improvement were metformin treatment and increase in circulating adiponectin levels.Among metformin treated patients: AI decreased significantly during the study. ALP and ALT decreased during initial 4-month treatment period, however raised to the pretreatment levels after 12 months. Serum adiponectin level tended to increase during treatment period with metformin.
Metformin treatment was associated with significant decrease in AI during one year treatment in NAFLD patients. These beneficial vascular effects was associated with exposure to metformin per se as well as change in adiponectin levels suggesting that metformin may mediate its vascular effects via glycemic control-independent mechanisms.
胰岛素抵抗(IR)是非酒精性脂肪性肝病(NAFLD)患者动脉粥样硬化发展和进展的主要驱动力。因此,纠正 IR 是一个相关的治疗靶点。我们进行了目前的试验,以评估 12 个月的二甲双胍治疗是否能改善 NAFLD 患者的血管僵硬,并评估这种改善是否与血糖控制、胰岛素抵抗或循环脂联素的变化有关。
在随机、安慰剂对照研究中,63 名 NAFLD 患者被分配到两组之一:组 1 每天接受二甲双胍治疗;组 2 接受安慰剂。使用 SphygmoCor(版本 7.1,AtCor Medical,悉尼,澳大利亚)在基线、治疗 4 个月和 12 个月时进行中心主动脉增强指数(AI)。测定代谢参数、胰岛素抵抗标志物和血清脂联素水平。
在安慰剂组中:AI 在治疗期间没有改善。肝功能和脂联素水平在研究期间没有变化。在多元线性回归分析中,动脉僵硬改善的独立预测因子是二甲双胍治疗和循环脂联素水平的增加。在接受二甲双胍治疗的患者中:AI 在研究期间显著下降。ALP 和 ALT 在最初的 4 个月治疗期间下降,但在 12 个月后恢复到治疗前水平。血清脂联素水平在二甲双胍治疗期间有升高的趋势。
在 NAFLD 患者的一年治疗中,二甲双胍治疗与 AI 的显著下降有关。这些有益的血管效应与二甲双胍本身的暴露以及脂联素水平的变化有关,这表明二甲双胍可能通过血糖控制以外的机制发挥其血管作用。