Literature DB >> 25794572

New medical treatment strategies for nonalcoholic steatohepatitis.

Michael Fuchs1.   

Abstract

OPINION STATEMENT: Nonalcoholic steatohepatitis (NASH) is a severe form of fatty liver disease unrelated to chronic alcohol consumption. As nonalcoholic fatty liver disease (NAFLD) has reached epidemic proportions and is becoming the most common cause for chronic liver disease, NASH likely will replace chronic hepatitis C as leading indication for liver cirrhosis and liver transplantation in this decade. Despite this alarming trend, effective treatment is lacking and continues to rely on dietary interventions and physical exercise, known to be of limited effect. Hence, there is an urgent need for safe pharmacologic therapy that successfully reverses or prevents progression of liver injury and fibrosis in patients with NASH. Employing emerging concepts of disease development and progression that involve in parallel ongoing events originating from the liver, adipose tissue, and intestine will ultimately promote the development of effective agents for targeted therapies for NASH. Novel agents must be safe, optimally dosed, and finally pass clinical trials providing proof of concept and efficacy. In the case of NASH, trial design is not necessarily straightforward as surrogate end points to predict clinical benefits are not yet established. The level of unmet needs for NASH goes however even beyond therapeutic agents and also includes patient and physician awareness. This article focuses on identifying potential pathophysiology-guided targets for medical therapy of NASH.

Entities:  

Year:  2015        PMID: 25794572     DOI: 10.1007/s11938-015-0053-z

Source DB:  PubMed          Journal:  Curr Treat Options Gastroenterol        ISSN: 1092-8472


  95 in total

1.  Meta-analysis: natural history of non-alcoholic fatty liver disease (NAFLD) and diagnostic accuracy of non-invasive tests for liver disease severity.

Authors:  Giovanni Musso; Roberto Gambino; Maurizio Cassader; Gianfranco Pagano
Journal:  Ann Med       Date:  2010-11-02       Impact factor: 4.709

2.  Autophagy and hepatic stellate cell activation - partners in crime?

Authors:  Christine C Hsu; Robert F Schwabe
Journal:  J Hepatol       Date:  2011-08-19       Impact factor: 25.083

3.  Elevated hepatic fatty acid oxidation, high plasma fibroblast growth factor 21, and fasting bile acids in nonalcoholic steatohepatitis.

Authors:  Srinivasan Dasarathy; Yu Yang; Arthur J McCullough; Susan Marczewski; Carole Bennett; Satish C Kalhan
Journal:  Eur J Gastroenterol Hepatol       Date:  2011-05       Impact factor: 2.566

4.  Lysyl oxidase and collagenase in experimental acute and chronic liver injury.

Authors:  E A Carter; M J McCarron; E Alpert; K J Isselbacher
Journal:  Gastroenterology       Date:  1982-03       Impact factor: 22.682

5.  Essential metabolic, anti-inflammatory, and anti-tumorigenic functions of miR-122 in liver.

Authors:  Shu-Hao Hsu; Bo Wang; Janaiah Kota; Jianhua Yu; Stefan Costinean; Huban Kutay; Lianbo Yu; Shoumei Bai; Krista La Perle; Raghu R Chivukula; Hsiaoyin Mao; Min Wei; K Reed Clark; Jerry R Mendell; Michael A Caligiuri; Samson T Jacob; Joshua T Mendell; Kalpana Ghoshal
Journal:  J Clin Invest       Date:  2012-07-23       Impact factor: 14.808

6.  Systemic inflammation in nonalcoholic fatty liver disease is characterized by elevated levels of CCL2.

Authors:  John Willy Haukeland; Jan Kristian Damås; Zbigniew Konopski; Else Marit Løberg; Terese Haaland; Ingeborg Goverud; Peter A Torjesen; Kåre Birkeland; Kristian Bjøro; Pål Aukrust
Journal:  J Hepatol       Date:  2006-03-20       Impact factor: 25.083

7.  Benefits of exenatide on obesity and non-alcoholic fatty liver disease with elevated liver enzymes in patients with type 2 diabetes.

Authors:  Ning Shao; Hong Yu Kuang; Ming Hao; Xin Yuan Gao; Wen Jian Lin; Wei Zou
Journal:  Diabetes Metab Res Rev       Date:  2014-09       Impact factor: 4.876

8.  Pharmacological inhibition of the chemokine CXCL16 diminishes liver macrophage infiltration and steatohepatitis in chronic hepatic injury.

Authors:  Alexander Wehr; Christer Baeck; Florian Ulmer; Nikolaus Gassler; Kanishka Hittatiya; Tom Luedde; Ulf Peter Neumann; Christian Trautwein; Frank Tacke
Journal:  PLoS One       Date:  2014-11-05       Impact factor: 3.240

9.  Cannabinoid receptor type 2 functional variant influences liver damage in children with non-alcoholic fatty liver disease.

Authors:  Francesca Rossi; Giulia Bellini; Anna Alisi; Arianna Alterio; Sabatino Maione; Laura Perrone; Franco Locatelli; Emanuele Miraglia del Giudice; Valerio Nobili
Journal:  PLoS One       Date:  2012-08-23       Impact factor: 3.240

10.  Dual peroxisome proliferator-activated receptor α/δ agonist GFT505 improves hepatic and peripheral insulin sensitivity in abdominally obese subjects.

Authors:  Bertrand Cariou; Rémy Hanf; Stéphanie Lambert-Porcheron; Yassine Zaïr; Valérie Sauvinet; Benoit Noël; Laurent Flet; Hubert Vidal; Bart Staels; Martine Laville
Journal:  Diabetes Care       Date:  2013-05-28       Impact factor: 19.112

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