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Nonalcoholic-Fatty-Liver-Disease and Nonalcoholic Steatohepatitis: Successful Development of Pharmacological Treatment Will Depend on Translational Research

机译:非酒精性脂肪肝疾病和非酒精脂肪肝炎:成功发展药理学治疗将取决于翻译研究

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Background: Nonalcoholic-fatty-liver-disease/nonalcoholic steatohepatitis (NAFLD/NASH) is expected to become the leading liver disease worldwide. Typical liver-related complications are fibrosis, cirrhosis, and the development of hepatocellular cancer (HCC) with the need for liver transplantation. Up to now there is no approved pharmacotherapy. Indeed, this might be due to the complexity of this disease. While the cheapest therapeutic approach is still a lifestyle change leading to weight loss, the proportion of people achieving sufficient weight reduction without additional support is low. Newly developed drugs are expensive and lack a breakthrough in therapeutic success. One reason might be that drugs developed often derive from murine models. Unfortunately, there is little overlap between genes in human and mice that are responsible for the development of NAFLD/NASH. This review aims at summarizing latest developments as well as stress again that more translational research is necessary. Summary: Therapy of NAFLD/NASH is easy and very complex at the same time, as the current main target is weight reduction. Since this is in fact not easily achieved and maintained by many affected individuals, pharmacotherapy to halt the progression of NAFLD/NASH is urgently warranted. More translational studies are needed to understand the metabolic mechanisms and interactions between the liver, gut, oxidative stress and the processes leading to NAFLD progression and HCC development, even in the absence of cirrhosis. (C) 2018 S. Karger AG, Basel
机译:背景:预计非酒精性 - 脂肪肝病/非酒精脂肪肝炎(NAFLD / NASH)将成为全球领先的肝病。典型的肝脏相关并发症是纤维化,肝硬化和肝细胞癌(HCC)的发育,需要肝移植。到目前为止,没有批准的药剂疗法。实际上,这可能是由于这种疾病的复杂性。虽然最便宜的治疗方法仍然是一个导致体重减轻的生活方式变化,但在没有额外支撑的情况下实现足够重量的人的比例很低。新开发的药物昂贵,缺乏治疗成功的突破。一个原因可能是毒药经常从鼠模型中获得。不幸的是,人类和小鼠的基因之间几乎没有重叠,这些是负责NAFLD / NASH的发展。该审查旨在总结最新的发展以及再次压力,即更多的翻译研究是必要的。发明内容:当前主要目标是减轻重量,NAFLD / NASH的治疗容易且非常复杂。由于这实际上是不容易实现和维持许多受影响的人,因此迫切需要药物治疗NAFLD / NASH的进展。即使在没有肝硬化的情况下,也需要更加平移的研究来了解肝脏,肠道,氧化应激与导致NAFLD进展和HCC开发的过程之间的代谢机制和相互作用。 (c)2018年S. Karger AG,巴塞尔

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