Treatment options for alcoholic and non-alcoholic fatty liver disease: A review

被引:297
作者
Singh, Sukhpreet [1 ]
Osna, Natalia A. [1 ,2 ]
Kharbanda, Kusum K. [1 ,2 ,3 ]
机构
[1] Vet Affairs Nebraska Western Iowa Hlth Care Syst, Res Serv, 151,4101 Woolworth Ave, Omaha, NE 68105 USA
[2] Nebraska Med Ctr, Dept Internal Med, Omaha, NE 68198 USA
[3] Nebraska Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
关键词
Alcoholic liver disease; non-alcoholic fatty; PLACEBO-CONTROLLED TRIAL; RANDOMIZED CONTROLLED-TRIAL; ADENOSYL-L-METHIONINE; FARNESOID-X-RECEPTOR; SHORT-TERM SURVIVAL; C VIRUS-INFECTION; AGONIST OBETICHOLIC ACID; LIFE-STYLE MODIFICATION; INDIVIDUAL PATIENT DATA; MESENCHYMAL STEM-CELLS;
D O I
10.3748/wjg.v23.i36.6549
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Alcoholic liver disease (ALD) and non-alcoholic fatty liver disease (NAFLD) are serious health problems worldwide. These two diseases have similar pathological spectra, ranging from simple steatosis to hepatitis to cirrhosis and hepatocellular carcinoma. Although most people with excessive alcohol or calorie intake display abnormal fat accumulation in the liver (simple steatosis), a small percentage develops progressive liver disease. Despite extensive research on understanding the pathophysiology of both these diseases there are still no targeted therapies available. The treatment for ALD remains as it was 50 years ago: abstinence, nutritional support and corticosteroids (or pentoxifylline as an alternative if steroids are contraindicated). As for NAFLD, the treatment modality is mainly directed toward weight loss and co-morbidity management. Therefore, new pathophysiology directed therapies are urgently needed. However, the involvement of several inter-related pathways in the pathogenesis of these diseases suggests that a single therapeutic agent is unlikely to be an effective treatment strategy. Hence, a combination therapy towards multiple targets would eventually be required. In this review, we delineate the treatment options in ALD and NAFLD, including various new targeted therapies that are currently under investigation. We hope that soon we will be having an effective multi-therapeutic regimen for each disease.
引用
收藏
页码:6549 / 6570
页数:22
相关论文
共 261 条
[1]
Nonalcoholic fatty liver disease [J].
Adams, LA ;
Angulo, P ;
Lindor, KD .
CANADIAN MEDICAL ASSOCIATION JOURNAL, 2005, 172 (07) :899-905
[2]
Vitamins E and C for the treatment of NASH: Duplication of results but lack of demonstration of efficacy [J].
Adams, LA ;
Angulo, P .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2003, 98 (11) :2348-2350
[3]
Effectiveness and safety of baclofen for maintenance of alcohol abstinence in alcohol-dependent patients with liver cirrhosis: randomised, double-blind controlled study [J].
Addolorato, Giovanni ;
Leggio, Lorenzo ;
Ferrulli, Anna ;
Cardone, Silvia ;
Vonghia, Luisa ;
Mirijello, Antonio ;
Abenavoli, Ludovico ;
D'Angelo, Cristina ;
Caputo, Fabio ;
Zambon, Antonella ;
Haber, Paul S. ;
Gasbarrini, Giovanni .
LANCET, 2007, 370 (9603) :1915-1922
[4]
Management of Alcohol Dependence in Patients with Liver Disease [J].
Addolorato, Giovanni ;
Mirijello, Antonio ;
Leggio, Lorenzo ;
Ferrulli, Anna ;
Landolfi, Raffaele .
CNS DRUGS, 2013, 27 (04) :287-299
[5]
Dose-Response Effect of Baclofen in Reducing Daily Alcohol Intake in Alcohol Dependence: Secondary Analysis of a Randomized, Double-Blind, Placebo-Controlled Trial [J].
Addolorato, Giovanni ;
Leggio, Lorenzo ;
Ferrulli, Anna ;
Cardone, Silvia ;
Bedogni, Giorgio ;
Caputo, Fabio ;
Gasbarrini, Giovanni ;
Landolfi, Raffaele .
ALCOHOL AND ALCOHOLISM, 2011, 46 (03) :312-317
[6]
Understanding and Treating Patients With Alcoholic Cirrhosis: An Update [J].
Addolorato, Giovanni ;
Russell, Marcia ;
Albano, Emanuele ;
Haber, Paul S. ;
Wands, Jack R. ;
Leggio, Lorenzo .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2009, 33 (07) :1136-1144
[7]
CCL20 mediates lipopolysaccharide induced liver injury and is a potential driver of inflammation and fibrosis in alcoholic hepatitis [J].
Affo, Silvia ;
Morales-Ibanez, Oriol ;
Rodrigo-Torres, Daniel ;
Altamirano, Jose ;
Blaya, Delia ;
Dapito, Dianne H. ;
Millan, Cristina ;
Coll, Mar ;
Caviglia, Jorge M. ;
Arroyo, Vicente ;
Caballeria, Juan ;
Schwabe, Robert F. ;
Gines, Pere ;
Bataller, Ramon ;
Sancho-Bru, Pau .
GUT, 2014, 63 (11) :1782-1792
[8]
Randomized, placebo-controlled trial of pioglitazone in nondiabetic subjects with nonalcoholic steatohepatitis [J].
Aithal, Guruprasad P. ;
Thomas, James A. ;
Kaye, Philip V. ;
Lawson, Adam ;
Ryder, Stephen D. ;
Spendlove, Ian ;
Austin, Andrew S. ;
Freeman, Jan G. ;
Morgan, Linda ;
Weeber, Jonathan .
GASTROENTEROLOGY, 2008, 135 (04) :1176-1184
[9]
Mesenchymal-Stem-Cell-Induced Immunoregulation Involves FAS-Ligand-/FAS-Mediated T Cell Apoptosis [J].
Akiyama, Kentaro ;
Chen, Chider ;
Wang, DanDan ;
Xu, Xingtian ;
Qu, Cunye ;
Yamaza, Takayoshi ;
Cai, Tao ;
Chen, WanJun ;
Sun, Lingyun ;
Shi, Songtao .
CELL STEM CELL, 2012, 10 (05) :544-555
[10]
Pentoxifylline improves short-term survival in severe acute alcoholic hepatitis: A double-blind, placebo-controlled trial [J].
Akriviadis, E ;
Botla, R ;
Briggs, W ;
Han, S ;
Reynolds, T ;
Shakil, O .
GASTROENTEROLOGY, 2000, 119 (06) :1637-1648