Yoon Hye-Jin, Cha Bong Soo
Hye-jin Yoon, Bong Soo Cha, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 120-752, South Korea.
World J Hepatol. 2014 Nov 27;6(11):800-11. doi: 10.4254/wjh.v6.i11.800.
Non-alcoholic fatty liver disease affects approximately one-third of the population worldwide, and its incidence continues to increase with the increasing prevalence of other metabolic disorders such as type 2 diabetes. As non-alcoholic fatty liver disease can progress to liver cirrhosis, its treatment is attracting greater attention. The pathogenesis of non-alcoholic fatty liver disease is closely associated with insulin resistance and dyslipidemia, especially hypertriglyceridemia. Increased serum levels of free fatty acid and glucose can cause oxidative stress in the liver and peripheral tissue, leading to ectopic fat accumulation, especially in the liver. In this review, we summarize the mechanism underlying the progression of hepatic steatosis to steatohepatitis and cirrhosis. We also discuss established drugs that are already being used to treat non-alcoholic fatty liver disease, in addition to newly discovered agents, with respect to their mechanisms of drug action, focusing mainly on hepatic insulin resistance. As well, we review clinical data that demonstrate the efficacy of these drugs, together with improvements in biochemical or histological parameters.
非酒精性脂肪性肝病影响着全球约三分之一的人口,并且随着2型糖尿病等其他代谢紊乱患病率的上升,其发病率持续增加。由于非酒精性脂肪性肝病可进展为肝硬化,其治疗正受到越来越多的关注。非酒精性脂肪性肝病的发病机制与胰岛素抵抗和血脂异常密切相关,尤其是高甘油三酯血症。血清游离脂肪酸和葡萄糖水平升高可导致肝脏和外周组织的氧化应激,导致异位脂肪堆积,尤其是在肝脏。在这篇综述中,我们总结了肝脂肪变性进展为脂肪性肝炎和肝硬化的潜在机制。我们还讨论了已用于治疗非酒精性脂肪性肝病的既定药物,以及新发现的药物,涉及它们的药物作用机制,主要关注肝脏胰岛素抵抗。此外,我们回顾了证明这些药物疗效的临床数据,以及生化或组织学参数的改善情况。