Literature DB >> 14585234

Treatment of Nonalcoholic Fatty Liver Disease.

Suthat Liangpunsakul1, Naga Chalasani.   

Abstract

Nonalcoholic fatty liver disease (NAFLD) is very common in the United States, and in some patients it may lead to cirrhosis, liver failure, and liver cancer. NAFLD encompasses a spectrum of liver injury, ranging from steatosis to steatohepatitis, advanced fibrosis, and cirrhosis. Nonalcoholic steatohepatitis (NASH), an advanced form of NAFLD, histologically comprises steatosis, balloon degeneration, inflammation, and fibrosis in varying degrees. It is generally believed that simple steatosis is benign with minimal risk of progression, whereas NASH is progressive and can lead to cirrhosis. The commonly associated risk factors for NAFLD include obesity, hyperlipidemia, and diabetes mellitus. The pathogenesis of NAFLD and NASH is not fully known; however, current evidence suggests that insulin resistance and lipid peroxidation play a role in the pathogenesis of this condition. Currently, there are no proven effective therapies available for the treatment of NASH. Although there are numerous studies that have explored various treatments for NASH, these generally consist of small numbers of patients with suboptimal endpoints. Treatment strategies for NAFLD and NASH can be broadly divided into 1) treatment or control of underlying risk factors such as hyperlipidemia, diabetes mellitus, and obesity; and 2) specific pharmacologic therapy such as insulin sensitizers, antioxidants, or cytoprotective agents. Newer thiazolidinediones, such as rosiglitazone and pioglitazone, have shown promise in the treatment of NASH in pilot studies. However, these agents should not be used in clinical practice until their efficacy and safety are firmly established in larger studies. Despite encouraging initial studies, the recently completed multicenter, randomized, controlled trial failed to show any efficacy for ursodeoxycholic acid in the treatment of NASH. Other agents, such as vitamin E, betaine, probucol, and atorvastatin, have been explored as therapeutic agents for NASH. However, none of these studies have shown convincingly their utility in the treatment of NASH. Attempts to identify optimal therapy for patients with NASH are being vigorously pursued by the research community and important advances are expected within next several years. Until then, subjects should be advised to avoid alcohol, lose weight, and exercise regularly, and meticulous attention should be paid to the control of their risk factors such as diabetes and hyperlipidemia.

Entities:  

Year:  2003        PMID: 14585234     DOI: 10.1007/s11938-003-0047-0

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


  47 in total

Review 1.  Nonalcoholic fatty liver disease.

Authors:  Jeanne M Clark; Frederick L Brancati; Anna Mae Diehl
Journal:  Gastroenterology       Date:  2002-05       Impact factor: 22.682

2.  American Gastroenterological Association medical position statement: nonalcoholic fatty liver disease.

Authors: 
Journal:  Gastroenterology       Date:  2002-11       Impact factor: 22.682

3.  Vitamin E treatment of nonalcoholic steatohepatitis in children: a pilot study.

Authors:  J E Lavine
Journal:  J Pediatr       Date:  2000-06       Impact factor: 4.406

4.  Regression of liver steatosis following gastroplasty or gastric bypass for morbid obesity.

Authors:  I Ranløv; F Hardt
Journal:  Digestion       Date:  1990       Impact factor: 3.216

5.  Prevalence of and risk factors for hepatic steatosis in Northern Italy.

Authors:  S Bellentani; G Saccoccio; F Masutti; L S Crocè; G Brandi; F Sasso; G Cristanini; C Tiribelli
Journal:  Ann Intern Med       Date:  2000-01-18       Impact factor: 25.391

6.  Ninety patients with nonalcoholic steatohepatitis: insulin resistance, familial tendency, and severity of disease.

Authors:  I R Willner; B Waters; S R Patil; A Reuben; J Morelli; C A Riely
Journal:  Am J Gastroenterol       Date:  2001-10       Impact factor: 10.864

Review 7.  Animal models of steatosis.

Authors:  A Koteish; A M Diehl
Journal:  Semin Liver Dis       Date:  2001       Impact factor: 6.115

8.  Metformin in non-alcoholic steatohepatitis.

Authors:  G Marchesini; M Brizi; G Bianchi; S Tomassetti; M Zoli; N Melchionda
Journal:  Lancet       Date:  2001-09-15       Impact factor: 79.321

9.  Probucol in the treatment of non-alcoholic steatohepatitis: a double-blind randomized controlled study.

Authors:  Shahin Merat; Reza Malekzadeh; Masoud Reza Sohrabi; Masoud Sotoudeh; Nasser Rakhshani; Amir Ali Sohrabpour; Siavosh Naserimoghadam
Journal:  J Hepatol       Date:  2003-04       Impact factor: 25.083

10.  Orlistat in the treatment of NASH: a case series.

Authors:  Stephen A Harrison; Sanjay Ramrakhiani; Elizabeth M Brunt; Maan A Anbari; Cherise Cortese; Bruce R Bacon
Journal:  Am J Gastroenterol       Date:  2003-04       Impact factor: 10.864

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  5 in total

1.  Nonalcoholic fatty liver disease treated by gastroplasty.

Authors:  K Jaskiewicz; S Raczynska; R Rzepko; Z Sledziński
Journal:  Dig Dis Sci       Date:  2006-01       Impact factor: 3.199

2.  A Mitochondrial VDAC1-Based Peptide Greatly Suppresses Steatosis and NASH-Associated Pathologies in a Mouse Model.

Authors:  Srinivas Pittala; Yakov Krelin; Yael Kuperman; Varda Shoshan-Barmatz
Journal:  Mol Ther       Date:  2019-07-12       Impact factor: 11.454

3.  Treatment of mouse liver slices with cholestatic hepatotoxicants results in down-regulation of Fxr and its target genes.

Authors:  Ewa Szalowska; Geert Stoopen; Maria J Groot; Peter J M Hendriksen; Ad A C M Peijnenburg
Journal:  BMC Med Genomics       Date:  2013-10-10       Impact factor: 3.063

4.  Fimasartan Ameliorates Nonalcoholic Fatty Liver Disease through PPARδ Regulation in Hyperlipidemic and Hypertensive Conditions.

Authors:  Yong-Jik Lee; Yoo-Na Jang; Yoon-Mi Han; Hyun-Min Kim; Jong-Min Jeong; Hong Seog Seo
Journal:  PPAR Res       Date:  2017-03-13       Impact factor: 4.964

5.  RNF43/ZNRF3 loss predisposes to hepatocellular-carcinoma by impairing liver regeneration and altering the liver lipid metabolic ground-state.

Authors:  Germán Belenguer; Gianmarco Mastrogiovanni; Clare Pacini; Zoe Hall; Anna M Dowbaj; Robert Arnes-Benito; Aleksandra Sljukic; Nicole Prior; Sofia Kakava; Charles R Bradshaw; Susan Davies; Michele Vacca; Kourosh Saeb-Parsy; Bon-Kyoung Koo; Meritxell Huch
Journal:  Nat Commun       Date:  2022-01-17       Impact factor: 17.694

  5 in total

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