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Relation between augmentation index and adiponectin during one-year metformin treatment for nonalcoholic steatohepatosis: effects beyond glucose lowering?

机译:二甲双胍治疗非酒精性脂肪性肝病一年期间增强指数与脂联素之间的关系:除了降低血糖以外,还有其他效果吗?

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Background 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. Methods 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. Results 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. Conclusions 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 glicemic control-independent mechanisms. Trial registry no: NCT01084486
机译:背景技术胰岛素抵抗(IR)是非酒精性脂肪肝疾病(NAFLD)患者动脉粥样硬化发展和进程的主要驱动力。因此,IR的校正是相关的治疗目标。我们进行了当前试验,以评估12个月的二甲双胍治疗是否可以改善NAFLD患者的血管僵硬度,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改变有关。方法在随机,安慰剂对照研究中,将63例NAFLD患者分为两组:第一组每天接受二甲双胍治疗;第二组每天接受二甲双胍治疗。第2组接受安慰剂。使用SphygmoCor(7.1版,AtCor Medical,悉尼,澳大利亚)在基线,4个月和12个月治疗期间进行中枢主动脉增强指数(AI)。测定代谢参数,胰岛素抵抗标志物和血清脂联素水平。结果安慰剂组:AI在治疗期间没有改善。在研究过程中,肝功能和脂联素水平没有改变。在多元线性回归分析中,动脉僵硬度改善的独立预测因素是二甲双胍治疗和循环脂联素水平增加。在二甲双胍治疗的患者中:研究期间AI显着降低。在最初的4个月治疗期间ALP和ALT降低,但在12个月后升高至治疗前水平。二甲双胍治疗期间血清脂联素水平趋于升高。结论二甲双胍治疗与NAFLD患者一年治疗期间AI显着降低有关。这些有益的血管作用与二甲双胍本身的暴露以及脂联素水平的变化有关,表明二甲双胍可能通过非依赖于控制的机制介导其血管作用。试用注册号:NCT01084486

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