Noninvasive investigations for non alcoholic fatty liver disease and liver fibrosis
Non-alcoholic fatty liver disease (NAFLD) includes a spectrum of diseases that have insulin resistance in common and are associated with metabolic conditions such as obesity, type 2 diabetes mellitus, and dyslipidemia. NAFLD ranges from simple liver steatosis, which follows a benign course, to nonal...
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Veröffentlicht in: | World journal of gastroenterology : WJG 2010-10, Vol.16 (38), p.4784-4791 |
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creator | Fierbinteanu-Braticevici, Carmen Dina, Ion Petrisor, Ana Tribus, Laura Negreanu, Lucian Carstoiu, Catalin |
description | Non-alcoholic fatty liver disease (NAFLD) includes a spectrum of diseases that have insulin resistance in common and are associated with metabolic conditions such as obesity, type 2 diabetes mellitus, and dyslipidemia. NAFLD ranges from simple liver steatosis, which follows a benign course, to nonalcoholic steatohepatitis (NASH), a more severe entity, with necroinflammation and fibrosis, which can progress to cryptogenic cirrhosis and end-stage liver disease. Liver biopsy remains the gold standard for evaluating the degree of hepatic necroinflammation and fibrosis; however, several noninvasive investigations, such as serum biomarkers, have been developed to establish the diagnosis and also to evaluate treatment response. These markers are currently neither available in all centers nor validated in extensive studies. Examples include high-sensitivity C reactive protein and plasma pentraxin 3, which are associated with extensive liver fibrosis in NASH. Interleukin-6 correlates with inflammation, and cytokeratin-18 represents a marker of hepatocyte apoptosis (prominent in NASH and absent in simple steatosis). Tissue polypeptide specific antigen seems to have a clinical utility in the follow-up of obese patients with NASH. |
doi_str_mv | 10.3748/wjg.v16.i38.4784 |
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NAFLD ranges from simple liver steatosis, which follows a benign course, to nonalcoholic steatohepatitis (NASH), a more severe entity, with necroinflammation and fibrosis, which can progress to cryptogenic cirrhosis and end-stage liver disease. Liver biopsy remains the gold standard for evaluating the degree of hepatic necroinflammation and fibrosis; however, several noninvasive investigations, such as serum biomarkers, have been developed to establish the diagnosis and also to evaluate treatment response. These markers are currently neither available in all centers nor validated in extensive studies. Examples include high-sensitivity C reactive protein and plasma pentraxin 3, which are associated with extensive liver fibrosis in NASH. Interleukin-6 correlates with inflammation, and cytokeratin-18 represents a marker of hepatocyte apoptosis (prominent in NASH and absent in simple steatosis). Tissue polypeptide specific antigen seems to have a clinical utility in the follow-up of obese patients with NASH.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v16.i38.4784</identifier><identifier>PMID: 20939106</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Co., Limited</publisher><subject>Biomarkers - blood ; Diagnostic Tests, Routine ; Fatty Liver - diagnosis ; Fatty Liver - etiology ; Fatty Liver - physiopathology ; Humans ; Liver - pathology ; Liver Cirrhosis - diagnosis ; Liver Cirrhosis - etiology ; Liver Cirrhosis - physiopathology ; Obesity - complications ; Obesity - physiopathology ; Topic Highlight</subject><ispartof>World journal of gastroenterology : WJG, 2010-10, Vol.16 (38), p.4784-4791</ispartof><rights>2010 Baishideng Publishing Group Co., Limited. All rights reserved. 2010</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-4f894691e014f61bfcf710fddd3b29889c481efacae53a87ec245e747aac42cd3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955247/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955247/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20939106$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fierbinteanu-Braticevici, Carmen</creatorcontrib><creatorcontrib>Dina, Ion</creatorcontrib><creatorcontrib>Petrisor, Ana</creatorcontrib><creatorcontrib>Tribus, Laura</creatorcontrib><creatorcontrib>Negreanu, Lucian</creatorcontrib><creatorcontrib>Carstoiu, Catalin</creatorcontrib><title>Noninvasive investigations for non alcoholic fatty liver disease and liver fibrosis</title><title>World journal of gastroenterology : WJG</title><addtitle>World J Gastroenterol</addtitle><description>Non-alcoholic fatty liver disease (NAFLD) includes a spectrum of diseases that have insulin resistance in common and are associated with metabolic conditions such as obesity, type 2 diabetes mellitus, and dyslipidemia. NAFLD ranges from simple liver steatosis, which follows a benign course, to nonalcoholic steatohepatitis (NASH), a more severe entity, with necroinflammation and fibrosis, which can progress to cryptogenic cirrhosis and end-stage liver disease. Liver biopsy remains the gold standard for evaluating the degree of hepatic necroinflammation and fibrosis; however, several noninvasive investigations, such as serum biomarkers, have been developed to establish the diagnosis and also to evaluate treatment response. These markers are currently neither available in all centers nor validated in extensive studies. Examples include high-sensitivity C reactive protein and plasma pentraxin 3, which are associated with extensive liver fibrosis in NASH. Interleukin-6 correlates with inflammation, and cytokeratin-18 represents a marker of hepatocyte apoptosis (prominent in NASH and absent in simple steatosis). Tissue polypeptide specific antigen seems to have a clinical utility in the follow-up of obese patients with NASH.</description><subject>Biomarkers - blood</subject><subject>Diagnostic Tests, Routine</subject><subject>Fatty Liver - diagnosis</subject><subject>Fatty Liver - etiology</subject><subject>Fatty Liver - physiopathology</subject><subject>Humans</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver Cirrhosis - etiology</subject><subject>Liver Cirrhosis - physiopathology</subject><subject>Obesity - complications</subject><subject>Obesity - physiopathology</subject><subject>Topic Highlight</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkTtPwzAUhS0EoqWwM6FsTAl-JbYXJIR4SRUMwGw5jt26Su0Sp0H997hqqWCyZZ977r3nA-ASwYIwym--F7NiQFXhCC8o4_QIjDFGIsecwmMwRhCyXBDMRuAsxgWEmJASn4IRhoIIBKsxeH8N3vlBRTeYLF1M7N1M9S74mNnQZT74TLU6zEPrdGZV32-yNmm7rHHRqGgy5Zv9i3V1F6KL5-DEqjaai_05AZ-PDx_3z_n07enl_m6aayLKPqeWC1oJZCCitkK11ZYhaJumITUWnAtNOTJWaWVKojgzGtPSMMqU0hTrhkzA7c53ta6XptHG951q5apzS9VtZFBO_v_xbi5nYZBYlCWmLBlc7w268LVOq8uli9q0rfImrKNkJWPboFBSwp1Spw1jZ-yhC4Jyi0ImFDKhkAmF3KJIJVd_pzsU_GZPfgAYOomp</recordid><startdate>20101014</startdate><enddate>20101014</enddate><creator>Fierbinteanu-Braticevici, Carmen</creator><creator>Dina, Ion</creator><creator>Petrisor, Ana</creator><creator>Tribus, Laura</creator><creator>Negreanu, Lucian</creator><creator>Carstoiu, Catalin</creator><general>Baishideng Publishing Group Co., Limited</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20101014</creationdate><title>Noninvasive investigations for non alcoholic fatty liver disease and liver fibrosis</title><author>Fierbinteanu-Braticevici, Carmen ; Dina, Ion ; Petrisor, Ana ; Tribus, Laura ; Negreanu, Lucian ; Carstoiu, Catalin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-4f894691e014f61bfcf710fddd3b29889c481efacae53a87ec245e747aac42cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Biomarkers - blood</topic><topic>Diagnostic Tests, Routine</topic><topic>Fatty Liver - diagnosis</topic><topic>Fatty Liver - etiology</topic><topic>Fatty Liver - physiopathology</topic><topic>Humans</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>Liver Cirrhosis - etiology</topic><topic>Liver Cirrhosis - physiopathology</topic><topic>Obesity - complications</topic><topic>Obesity - physiopathology</topic><topic>Topic Highlight</topic><toplevel>online_resources</toplevel><creatorcontrib>Fierbinteanu-Braticevici, Carmen</creatorcontrib><creatorcontrib>Dina, Ion</creatorcontrib><creatorcontrib>Petrisor, Ana</creatorcontrib><creatorcontrib>Tribus, Laura</creatorcontrib><creatorcontrib>Negreanu, Lucian</creatorcontrib><creatorcontrib>Carstoiu, Catalin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fierbinteanu-Braticevici, Carmen</au><au>Dina, Ion</au><au>Petrisor, Ana</au><au>Tribus, Laura</au><au>Negreanu, Lucian</au><au>Carstoiu, Catalin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Noninvasive investigations for non alcoholic fatty liver disease and liver fibrosis</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World J Gastroenterol</addtitle><date>2010-10-14</date><risdate>2010</risdate><volume>16</volume><issue>38</issue><spage>4784</spage><epage>4791</epage><pages>4784-4791</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>Non-alcoholic fatty liver disease (NAFLD) includes a spectrum of diseases that have insulin resistance in common and are associated with metabolic conditions such as obesity, type 2 diabetes mellitus, and dyslipidemia. NAFLD ranges from simple liver steatosis, which follows a benign course, to nonalcoholic steatohepatitis (NASH), a more severe entity, with necroinflammation and fibrosis, which can progress to cryptogenic cirrhosis and end-stage liver disease. Liver biopsy remains the gold standard for evaluating the degree of hepatic necroinflammation and fibrosis; however, several noninvasive investigations, such as serum biomarkers, have been developed to establish the diagnosis and also to evaluate treatment response. These markers are currently neither available in all centers nor validated in extensive studies. Examples include high-sensitivity C reactive protein and plasma pentraxin 3, which are associated with extensive liver fibrosis in NASH. Interleukin-6 correlates with inflammation, and cytokeratin-18 represents a marker of hepatocyte apoptosis (prominent in NASH and absent in simple steatosis). 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subjects | Biomarkers - blood Diagnostic Tests, Routine Fatty Liver - diagnosis Fatty Liver - etiology Fatty Liver - physiopathology Humans Liver - pathology Liver Cirrhosis - diagnosis Liver Cirrhosis - etiology Liver Cirrhosis - physiopathology Obesity - complications Obesity - physiopathology Topic Highlight |
title | Noninvasive investigations for non alcoholic fatty liver disease and liver fibrosis |
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