Literature DB >> 19845871

Non-alcoholic fatty liver disease from pathogenesis to management: an update.

G Musso1, R Gambino, M Cassader.   

Abstract

Non-alcoholic fatty liver disease (NAFLD), the most common chronic liver disease in the Western world, is tightly associated with obesity and metabolic syndrome. NAFLD entails an increased cardiometabolic and liver-related risk, the latter regarding almost exclusively non-alcoholic steatohepatitis (NASH), the progressive form of NAFLD. Pathogenetic models encompass altered hepatic lipid partitioning and adipokine action, increased oxidative stress, free fatty acid lipotoxicity. On this basis, lifestyle-, drug- or surgically induced weight loss, insulin sensitizers, antioxidants, lipid-lowering drugs have been evaluated in NAFLD/NASH. Most trials are small, of short duration, nonrandomized, without histological end points, thus limiting assessment of long-term safety and efficacy of proposed treatments. All NAFLD patients should be evaluated for their metabolic, cardiovascular and liver-related risk. Liver biopsy remains the gold standard for staging NAFLD, but non-invasive methods are under intense development. Weight loss through lifestyle intervention is the initial approach, because of established efficacy on NAFLD-associated cardiometabolic abnormalities, and to emerging benefits on necroinflammation and overall disease activity in NASH. Bariatric surgery warrants further evaluation before it can be routinely considered in morbidly obese NASH. Larger- and longer-duration randomized trials assessing safety and benefits of drugs on patient-oriented outcomes are needed before pharmacological treatment can be routinely recommended for NASH.

Entities:  

Mesh:

Year:  2009        PMID: 19845871     DOI: 10.1111/j.1467-789X.2009.00657.x

Source DB:  PubMed          Journal:  Obes Rev        ISSN: 1467-7881            Impact factor:   9.213


  55 in total

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Authors:  Lu Zeng; Wai J Tang; Jin J Yin; Bei J Zhou
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Review 5.  Gender specific medicine in liver diseases: a point of view.

Authors:  Marilena Durazzo; Paola Belci; Alessandro Collo; Vanessa Prandi; Erika Pistone; Maria Martorana; Roberto Gambino; Simona Bo
Journal:  World J Gastroenterol       Date:  2014-03-07       Impact factor: 5.742

6.  Serum lipocalin-2, cathepsin S and chemerin levels and nonalcoholic fatty liver disease.

Authors:  Zi Ye; Suijun Wang; Zhen Yang; Min He; Shuo Zhang; Weiwei Zhang; Jie Wen; Qin Li; Ying Huang; Xuanchun Wang; Bin Lu; Zhaoyun Zhang; Qing Su; Renming Hu
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7.  Probucol ameliorates the development of nonalcoholic steatohepatitis in rats fed high-fat diets.

Authors:  Rong Wu; Wei Zhang; Bo Liu; Jing Gao; Xiao-Qiu Xiao; Feng Zhang; Hua-Mei Zhou; Xiao-Ling Wu; Xia Zhang
Journal:  Dig Dis Sci       Date:  2012-08-10       Impact factor: 3.199

Review 8.  Pathogenesis of nonalcoholic steatohepatitis.

Authors:  Wensheng Liu; Robert D Baker; Tavleen Bhatia; Lixin Zhu; Susan S Baker
Journal:  Cell Mol Life Sci       Date:  2016-02-19       Impact factor: 9.261

Review 9.  Focus on emerging drugs for the treatment of patients with non-alcoholic fatty liver disease.

Authors:  Alessandro Federico; Claudio Zulli; Ilario de Sio; Anna Del Prete; Marcello Dallio; Mario Masarone; Carmela Loguercio
Journal:  World J Gastroenterol       Date:  2014-12-07       Impact factor: 5.742

10.  Emodin attenuates systemic and liver inflammation in hyperlipidemic mice administrated with lipopolysaccharides.

Authors:  Xuemei Jia; Stephen Iwanowycz; Junfeng Wang; Fatma Saaoud; Fang Yu; Yuzhen Wang; Jun Hu; Saurabh Chatterjee; Qian Wang; Daping Fan
Journal:  Exp Biol Med (Maywood)       Date:  2014-04-16
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