Nonalcoholic fatty liver disease: pathogenesis and the role of antioxidants
Nonalcoholic fatty liver disease (NAFLD) includes a wide spectrum of liver injury ranging from simple steatosis to steatohepatitis, fibrosis, and cirrhosis. Whereas simple steatosis has a benign clinical course, steatohepatitis is a recognized cause of progressive liver fibrosis and can develop into...
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Veröffentlicht in: | Nutrition reviews 2002-09, Vol.60 (9), p.289-293 |
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description | Nonalcoholic fatty liver disease (NAFLD) includes a wide spectrum of liver injury ranging from simple steatosis to steatohepatitis, fibrosis, and cirrhosis. Whereas simple steatosis has a benign clinical course, steatohepatitis is a recognized cause of progressive liver fibrosis and can develop into cirrhosis. NAFLD and nonalcoholic steatohepatitis (NASH) are the two most common chronic liver diseases in United States general population with a prevalence of 20% and 3%, respectively. Hepatic steatosis is frequently associated with obesity, type 2 diabetes, and hyperlipidemia with insulin resistance as a key pathogenic factor. A two‐hit theory best describes the progression from simple steatosis to NASH, fibrosis, or cirrhosis. These two hits consist of the accumulation of excessive hepatic fat primarily owing to insulin resistance, and oxidative stress owing to reactive oxygen species (ROS). Mitochondria are the major cellular source of ROS in cases of NASH. Currently, treatment is focused on modifying risk factors such as obesity, diabetes mellitus, and hyperlipidemia. Antioxidants such as vitamin E, N‐acetylcysteine, betaine, and others may be beneficial in the treatment of NASH. |
doi_str_mv | 10.1301/002966402320387224 |
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Whereas simple steatosis has a benign clinical course, steatohepatitis is a recognized cause of progressive liver fibrosis and can develop into cirrhosis. NAFLD and nonalcoholic steatohepatitis (NASH) are the two most common chronic liver diseases in United States general population with a prevalence of 20% and 3%, respectively. Hepatic steatosis is frequently associated with obesity, type 2 diabetes, and hyperlipidemia with insulin resistance as a key pathogenic factor. A two‐hit theory best describes the progression from simple steatosis to NASH, fibrosis, or cirrhosis. These two hits consist of the accumulation of excessive hepatic fat primarily owing to insulin resistance, and oxidative stress owing to reactive oxygen species (ROS). Mitochondria are the major cellular source of ROS in cases of NASH. Currently, treatment is focused on modifying risk factors such as obesity, diabetes mellitus, and hyperlipidemia. Antioxidants such as vitamin E, N‐acetylcysteine, betaine, and others may be beneficial in the treatment of NASH.</description><identifier>ISSN: 0029-6643</identifier><identifier>EISSN: 1753-4887</identifier><identifier>DOI: 10.1301/002966402320387224</identifier><identifier>PMID: 12296456</identifier><identifier>CODEN: NUREA8</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>amino acid derivatives ; amino acid metabolism ; Antioxidants ; Antioxidants - therapeutic use ; betaine ; Biological and medical sciences ; cirrhosis ; diabetes ; diet therapy ; Disease ; fatty liver ; Fatty Liver - pathology ; Fatty Liver - therapy ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; hyperlipidemia ; insulin resistance ; Liver ; liver cirrhosis ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Medical sciences ; N-acetylcysteine ; nonalcoholic fatty liver disease (NAFLD) ; nonalcoholic steatohepatitis (NASH) ; Nutrition ; obesity ; Other diseases. Semiology ; oxidative stress ; Pathology ; progressive liver fibrosis ; risk factors ; steatohepatitis ; vitamin E</subject><ispartof>Nutrition reviews, 2002-09, Vol.60 (9), p.289-293</ispartof><rights>2002 International Life Sciences Institute</rights><rights>2002 INIST-CNRS</rights><rights>Copyright International Life Sciences Institute and Nutrition Foundation Sep 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5769-5a4c26d14b34287daa221c81ea92de66ffbededf0d6a5bae67e82a0f305eec6b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1301%2F002966402320387224$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1301%2F002966402320387224$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13906800$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12296456$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mehta, K</creatorcontrib><creatorcontrib>Van Thiel, D.H</creatorcontrib><creatorcontrib>Shah, N</creatorcontrib><creatorcontrib>Mobarhan, S</creatorcontrib><title>Nonalcoholic fatty liver disease: pathogenesis and the role of antioxidants</title><title>Nutrition reviews</title><addtitle>Nutr Rev</addtitle><description>Nonalcoholic fatty liver disease (NAFLD) includes a wide spectrum of liver injury ranging from simple steatosis to steatohepatitis, fibrosis, and cirrhosis. Whereas simple steatosis has a benign clinical course, steatohepatitis is a recognized cause of progressive liver fibrosis and can develop into cirrhosis. NAFLD and nonalcoholic steatohepatitis (NASH) are the two most common chronic liver diseases in United States general population with a prevalence of 20% and 3%, respectively. Hepatic steatosis is frequently associated with obesity, type 2 diabetes, and hyperlipidemia with insulin resistance as a key pathogenic factor. A two‐hit theory best describes the progression from simple steatosis to NASH, fibrosis, or cirrhosis. These two hits consist of the accumulation of excessive hepatic fat primarily owing to insulin resistance, and oxidative stress owing to reactive oxygen species (ROS). Mitochondria are the major cellular source of ROS in cases of NASH. Currently, treatment is focused on modifying risk factors such as obesity, diabetes mellitus, and hyperlipidemia. Antioxidants such as vitamin E, N‐acetylcysteine, betaine, and others may be beneficial in the treatment of NASH.</description><subject>amino acid derivatives</subject><subject>amino acid metabolism</subject><subject>Antioxidants</subject><subject>Antioxidants - therapeutic use</subject><subject>betaine</subject><subject>Biological and medical sciences</subject><subject>cirrhosis</subject><subject>diabetes</subject><subject>diet therapy</subject><subject>Disease</subject><subject>fatty liver</subject><subject>Fatty Liver - pathology</subject><subject>Fatty Liver - therapy</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>hyperlipidemia</subject><subject>insulin resistance</subject><subject>Liver</subject><subject>liver cirrhosis</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Medical sciences</subject><subject>N-acetylcysteine</subject><subject>nonalcoholic fatty liver disease (NAFLD)</subject><subject>nonalcoholic steatohepatitis (NASH)</subject><subject>Nutrition</subject><subject>obesity</subject><subject>Other diseases. Semiology</subject><subject>oxidative stress</subject><subject>Pathology</subject><subject>progressive liver fibrosis</subject><subject>risk factors</subject><subject>steatohepatitis</subject><subject>vitamin E</subject><issn>0029-6643</issn><issn>1753-4887</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqN0E1v1DAQBmALgei28Ac4QIRUbgF_xU56Q6UUtGWRKCuO1sQZd12y8WJnofvv8SorKsEF-TCy9LwezxDyjNHXTFD2hlLeKCUpF5yKWnMuH5AZ05UoZV3rh2S2B2UW4ogcp3RLKWW8EY_JEeM5KSs1I_NFGKC3YRV6bwsH47grev8TY9H5hJDwrNjAuAo3OGDyqYChK8YVFjH0WASX76MPd77LNT0hjxz0CZ8e6glZvr_4ev6hvPp8-fH87VVpK62asgJpueqYbIXkte4AOGe2ZggN71Ap51rssHO0U1C1gEpjzYE6QStEq1pxQl5N725i-LHFNJq1Txb7HgYM22Q0Z_k0LMOXf8HbsI153mQyEJxJyTPiE7IxpBTRmU30a4g7w6jZ79n8u-ccen54eduusbuPHBabwekBQLLQuwiD9eneiYaqmtLs9OR--R53_9HaLJZfLnjd5GQ5JX0a8e5PEuJ3o7TQlfm2uDTy3XxeX-tPZj_ni8k7CAZuYv7N8prTfRsqcodK_Aav36ym</recordid><startdate>200209</startdate><enddate>200209</enddate><creator>Mehta, K</creator><creator>Van Thiel, D.H</creator><creator>Shah, N</creator><creator>Mobarhan, S</creator><general>Blackwell Publishing Ltd</general><general>International Life Sciences Institute</general><general>Oxford University Press</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0K</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>200209</creationdate><title>Nonalcoholic fatty liver disease: pathogenesis and the role of antioxidants</title><author>Mehta, K ; Van Thiel, D.H ; Shah, N ; Mobarhan, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5769-5a4c26d14b34287daa221c81ea92de66ffbededf0d6a5bae67e82a0f305eec6b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>amino acid derivatives</topic><topic>amino acid metabolism</topic><topic>Antioxidants</topic><topic>Antioxidants - therapeutic use</topic><topic>betaine</topic><topic>Biological and medical sciences</topic><topic>cirrhosis</topic><topic>diabetes</topic><topic>diet therapy</topic><topic>Disease</topic><topic>fatty liver</topic><topic>Fatty Liver - pathology</topic><topic>Fatty Liver - therapy</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>hyperlipidemia</topic><topic>insulin resistance</topic><topic>Liver</topic><topic>liver cirrhosis</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical sciences</topic><topic>N-acetylcysteine</topic><topic>nonalcoholic fatty liver disease (NAFLD)</topic><topic>nonalcoholic steatohepatitis (NASH)</topic><topic>Nutrition</topic><topic>obesity</topic><topic>Other diseases. Semiology</topic><topic>oxidative stress</topic><topic>Pathology</topic><topic>progressive liver fibrosis</topic><topic>risk factors</topic><topic>steatohepatitis</topic><topic>vitamin E</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mehta, K</creatorcontrib><creatorcontrib>Van Thiel, D.H</creatorcontrib><creatorcontrib>Shah, N</creatorcontrib><creatorcontrib>Mobarhan, S</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Agricultural Science Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Nutrition reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mehta, K</au><au>Van Thiel, D.H</au><au>Shah, N</au><au>Mobarhan, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonalcoholic fatty liver disease: pathogenesis and the role of antioxidants</atitle><jtitle>Nutrition reviews</jtitle><addtitle>Nutr Rev</addtitle><date>2002-09</date><risdate>2002</risdate><volume>60</volume><issue>9</issue><spage>289</spage><epage>293</epage><pages>289-293</pages><issn>0029-6643</issn><eissn>1753-4887</eissn><coden>NUREA8</coden><abstract>Nonalcoholic fatty liver disease (NAFLD) includes a wide spectrum of liver injury ranging from simple steatosis to steatohepatitis, fibrosis, and cirrhosis. Whereas simple steatosis has a benign clinical course, steatohepatitis is a recognized cause of progressive liver fibrosis and can develop into cirrhosis. NAFLD and nonalcoholic steatohepatitis (NASH) are the two most common chronic liver diseases in United States general population with a prevalence of 20% and 3%, respectively. Hepatic steatosis is frequently associated with obesity, type 2 diabetes, and hyperlipidemia with insulin resistance as a key pathogenic factor. A two‐hit theory best describes the progression from simple steatosis to NASH, fibrosis, or cirrhosis. These two hits consist of the accumulation of excessive hepatic fat primarily owing to insulin resistance, and oxidative stress owing to reactive oxygen species (ROS). Mitochondria are the major cellular source of ROS in cases of NASH. Currently, treatment is focused on modifying risk factors such as obesity, diabetes mellitus, and hyperlipidemia. Antioxidants such as vitamin E, N‐acetylcysteine, betaine, and others may be beneficial in the treatment of NASH.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12296456</pmid><doi>10.1301/002966402320387224</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | amino acid derivatives amino acid metabolism Antioxidants Antioxidants - therapeutic use betaine Biological and medical sciences cirrhosis diabetes diet therapy Disease fatty liver Fatty Liver - pathology Fatty Liver - therapy Gastroenterology. Liver. Pancreas. Abdomen Humans hyperlipidemia insulin resistance Liver liver cirrhosis Liver. Biliary tract. Portal circulation. Exocrine pancreas Medical sciences N-acetylcysteine nonalcoholic fatty liver disease (NAFLD) nonalcoholic steatohepatitis (NASH) Nutrition obesity Other diseases. Semiology oxidative stress Pathology progressive liver fibrosis risk factors steatohepatitis vitamin E |
title | Nonalcoholic fatty liver disease: pathogenesis and the role of antioxidants |
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