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Role of a cirrhosis risk score for the early prediction of fibrosis progression in hepatitis C patients with minimal liver disease
Background & Aims Fibrosis progression in patients with chronic hepatitis C (CHC) is highly variable. A Cirrhosis Risk Score (CRS) based on seven genetic variants has been recently developed for identifying patients at risk for cirrhosis. The objective of this study was to assess the role of the...
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Published in: | Journal of hepatology 2011-07, Vol.55 (1), p.38-44 |
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creator | Trépo, Eric Potthoff, Andrej Pradat, Pierre Bakshi, Rakesh Young, Bradford Lagier, Robert Moreno, Christophe Verset, Laurine Cross, Richard Degré, Delphine Lemmers, Arnaud Gustot, Thierry Berthillon, Pascale Rosenberg, William Trépo, Christian Sninsky, John Adler, Michael Wedemeyer, Heiner |
description | Background & Aims Fibrosis progression in patients with chronic hepatitis C (CHC) is highly variable. A Cirrhosis Risk Score (CRS) based on seven genetic variants has been recently developed for identifying patients at risk for cirrhosis. The objective of this study was to assess the role of the CRS for the early prediction of fibrosis progression in CHC patients with mild liver fibrosis. In addition, we evaluated the potential benefit, for prediction accuracy, of a recently described non-invasive fibrosis staging assay, the Enhanced Liver Fibrosis (ELF) test. Methods Two separate cohorts of HCV patients (Brussels, Belgium/Hannover, Germany) were retrospectively analyzed. Only patients with a fibrosis Ishak or METAVIR score of F0–F1 at baseline were included. Patients were classified as progressors if they showed an increase ⩾2 fibrosis stages at the second histological evaluation after a follow-up ⩾5 years. The CRS was calculated locally. Genotyping was performed by PCR and oligonucleotide ligation with the resulting signal detected with a Luminex® 200TM and computer analysis. Results In Brussels, 12/25 patients progressed (48%); similarly in Hannover, 16/31 (52%) patients progressed. In both sample sets, the CRS was significantly associated with fibrosis progression ( p = 0.050 in Brussels; p = 0.018 in Hannover). The ELF test was only a significant predictor in Hannover ( p = 0.015). In multivariate analysis the CRS remained the only variable associated with fibrosis progression (odds-ratio = 2.23, 95%CI 1.21–4.11 p = 0.01). Conclusions Although conducted on a limited number of patients, this study in two independent centres confirms that the CRS predicts fibrosis progression in initially mild CHC. |
doi_str_mv | 10.1016/j.jhep.2010.10.018 |
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A Cirrhosis Risk Score (CRS) based on seven genetic variants has been recently developed for identifying patients at risk for cirrhosis. The objective of this study was to assess the role of the CRS for the early prediction of fibrosis progression in CHC patients with mild liver fibrosis. In addition, we evaluated the potential benefit, for prediction accuracy, of a recently described non-invasive fibrosis staging assay, the Enhanced Liver Fibrosis (ELF) test. Methods Two separate cohorts of HCV patients (Brussels, Belgium/Hannover, Germany) were retrospectively analyzed. Only patients with a fibrosis Ishak or METAVIR score of F0–F1 at baseline were included. Patients were classified as progressors if they showed an increase ⩾2 fibrosis stages at the second histological evaluation after a follow-up ⩾5 years. The CRS was calculated locally. Genotyping was performed by PCR and oligonucleotide ligation with the resulting signal detected with a Luminex® 200TM and computer analysis. Results In Brussels, 12/25 patients progressed (48%); similarly in Hannover, 16/31 (52%) patients progressed. In both sample sets, the CRS was significantly associated with fibrosis progression ( p = 0.050 in Brussels; p = 0.018 in Hannover). The ELF test was only a significant predictor in Hannover ( p = 0.015). In multivariate analysis the CRS remained the only variable associated with fibrosis progression (odds-ratio = 2.23, 95%CI 1.21–4.11 p = 0.01). Conclusions Although conducted on a limited number of patients, this study in two independent centres confirms that the CRS predicts fibrosis progression in initially mild CHC.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2010.10.018</identifier><identifier>PMID: 21145859</identifier><identifier>CODEN: JOHEEC</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Biological and medical sciences ; Cirrhosis risk score (CRS) ; Cohort Studies ; Disease Progression ; Female ; Fibrosis progression ; Gastroenterology and Hepatology ; Gastroenterology. Liver. Pancreas. Abdomen ; Genetic Variation ; Hepatitis C ; Hepatitis C, Chronic - classification ; Hepatitis C, Chronic - complications ; Hepatitis C, Chronic - genetics ; Hepatitis C, Chronic - pathology ; Human viral diseases ; Humans ; Infectious diseases ; Liver Cirrhosis - classification ; Liver Cirrhosis - etiology ; Liver Cirrhosis - genetics ; Liver Cirrhosis - pathology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Minimal liver disease ; Multivariate Analysis ; Other diseases. Semiology ; Polymorphism, Single Nucleotide ; Retrospective Studies ; Risk Factors ; Viral diseases ; Viral hepatitis</subject><ispartof>Journal of hepatology, 2011-07, Vol.55 (1), p.38-44</ispartof><rights>European Association for the Study of the Liver</rights><rights>2010 European Association for the Study of the Liver</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-26635c4043c9130798577d05b5669655cda2c1e209db089653c18a922c1eee503</citedby><cites>FETCH-LOGICAL-c440t-26635c4043c9130798577d05b5669655cda2c1e209db089653c18a922c1eee503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24265960$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21145859$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Trépo, Eric</creatorcontrib><creatorcontrib>Potthoff, Andrej</creatorcontrib><creatorcontrib>Pradat, Pierre</creatorcontrib><creatorcontrib>Bakshi, Rakesh</creatorcontrib><creatorcontrib>Young, Bradford</creatorcontrib><creatorcontrib>Lagier, Robert</creatorcontrib><creatorcontrib>Moreno, Christophe</creatorcontrib><creatorcontrib>Verset, Laurine</creatorcontrib><creatorcontrib>Cross, Richard</creatorcontrib><creatorcontrib>Degré, Delphine</creatorcontrib><creatorcontrib>Lemmers, Arnaud</creatorcontrib><creatorcontrib>Gustot, Thierry</creatorcontrib><creatorcontrib>Berthillon, Pascale</creatorcontrib><creatorcontrib>Rosenberg, William</creatorcontrib><creatorcontrib>Trépo, Christian</creatorcontrib><creatorcontrib>Sninsky, John</creatorcontrib><creatorcontrib>Adler, Michael</creatorcontrib><creatorcontrib>Wedemeyer, Heiner</creatorcontrib><title>Role of a cirrhosis risk score for the early prediction of fibrosis progression in hepatitis C patients with minimal liver disease</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>Background & Aims Fibrosis progression in patients with chronic hepatitis C (CHC) is highly variable. A Cirrhosis Risk Score (CRS) based on seven genetic variants has been recently developed for identifying patients at risk for cirrhosis. The objective of this study was to assess the role of the CRS for the early prediction of fibrosis progression in CHC patients with mild liver fibrosis. In addition, we evaluated the potential benefit, for prediction accuracy, of a recently described non-invasive fibrosis staging assay, the Enhanced Liver Fibrosis (ELF) test. Methods Two separate cohorts of HCV patients (Brussels, Belgium/Hannover, Germany) were retrospectively analyzed. Only patients with a fibrosis Ishak or METAVIR score of F0–F1 at baseline were included. Patients were classified as progressors if they showed an increase ⩾2 fibrosis stages at the second histological evaluation after a follow-up ⩾5 years. The CRS was calculated locally. Genotyping was performed by PCR and oligonucleotide ligation with the resulting signal detected with a Luminex® 200TM and computer analysis. Results In Brussels, 12/25 patients progressed (48%); similarly in Hannover, 16/31 (52%) patients progressed. In both sample sets, the CRS was significantly associated with fibrosis progression ( p = 0.050 in Brussels; p = 0.018 in Hannover). The ELF test was only a significant predictor in Hannover ( p = 0.015). In multivariate analysis the CRS remained the only variable associated with fibrosis progression (odds-ratio = 2.23, 95%CI 1.21–4.11 p = 0.01). Conclusions Although conducted on a limited number of patients, this study in two independent centres confirms that the CRS predicts fibrosis progression in initially mild CHC.</description><subject>Biological and medical sciences</subject><subject>Cirrhosis risk score (CRS)</subject><subject>Cohort Studies</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Fibrosis progression</subject><subject>Gastroenterology and Hepatology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genetic Variation</subject><subject>Hepatitis C</subject><subject>Hepatitis C, Chronic - classification</subject><subject>Hepatitis C, Chronic - complications</subject><subject>Hepatitis C, Chronic - genetics</subject><subject>Hepatitis C, Chronic - pathology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Liver Cirrhosis - classification</subject><subject>Liver Cirrhosis - etiology</subject><subject>Liver Cirrhosis - genetics</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Minimal liver disease</subject><subject>Multivariate Analysis</subject><subject>Other diseases. Semiology</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kkuLFDEUhYMoTjv6B1xINuKq2ptUkqoCEYbGFwwIPtYhnbplp6e60uZWj_TWX24y3Sq4cJVwcs7NyUcYeypgKUCYl9vldoP7pYQ7YQmivccWwgBUYJS4zxbZ1FatbNoL9ohoCwA1dOohu5BCKN3qbsF-fooj8jhwx31IaRMpEE-Bbjj5mJAPMfF5gxxdGo98n7APfg5xKpEhrNOdf5_it4RERQ8Tz6XcHOZ8sOJlh9NM_EeYN3wXprBzIx_DLSbeB0JH-Jg9GNxI-OS8XrKvb998Wb2vrj---7C6uq68UjBX0phaewWq9p2ooela3TQ96LU2pjNa-95JL1BC16-hzUrtRes6WUREDfUle3Gam-t-PyDNdhfI4zi6CeOBbNtIpYQ0dXbKk9Pn91HCwe5T7p2OVoAt6O3WFvS2oC9aRp9Dz87jD-sd9n8iv1lnw_OzwZF345Dc5AP99SlpdGdKz1cnH2YYtwGTJZ8Z-ow-oZ9tH8P_e7z-J-7HjD3feINHpG08pCljtsKStGA_l09S_oiAPKRpof4FicS3TA</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Trépo, Eric</creator><creator>Potthoff, Andrej</creator><creator>Pradat, Pierre</creator><creator>Bakshi, Rakesh</creator><creator>Young, Bradford</creator><creator>Lagier, Robert</creator><creator>Moreno, Christophe</creator><creator>Verset, Laurine</creator><creator>Cross, Richard</creator><creator>Degré, Delphine</creator><creator>Lemmers, Arnaud</creator><creator>Gustot, Thierry</creator><creator>Berthillon, Pascale</creator><creator>Rosenberg, William</creator><creator>Trépo, Christian</creator><creator>Sninsky, John</creator><creator>Adler, Michael</creator><creator>Wedemeyer, Heiner</creator><general>Elsevier B.V</general><general>Elsevier</general><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>7X8</scope></search><sort><creationdate>20110701</creationdate><title>Role of a cirrhosis risk score for the early prediction of fibrosis progression in hepatitis C patients with minimal liver disease</title><author>Trépo, Eric ; Potthoff, Andrej ; Pradat, Pierre ; Bakshi, Rakesh ; Young, Bradford ; Lagier, Robert ; Moreno, Christophe ; Verset, Laurine ; Cross, Richard ; Degré, Delphine ; Lemmers, Arnaud ; Gustot, Thierry ; Berthillon, Pascale ; Rosenberg, William ; Trépo, Christian ; Sninsky, John ; Adler, Michael ; Wedemeyer, Heiner</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-26635c4043c9130798577d05b5669655cda2c1e209db089653c18a922c1eee503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biological and medical sciences</topic><topic>Cirrhosis risk score (CRS)</topic><topic>Cohort Studies</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Fibrosis progression</topic><topic>Gastroenterology and Hepatology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Genetic Variation</topic><topic>Hepatitis C</topic><topic>Hepatitis C, Chronic - classification</topic><topic>Hepatitis C, Chronic - complications</topic><topic>Hepatitis C, Chronic - genetics</topic><topic>Hepatitis C, Chronic - pathology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Liver Cirrhosis - classification</topic><topic>Liver Cirrhosis - etiology</topic><topic>Liver Cirrhosis - genetics</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Minimal liver disease</topic><topic>Multivariate Analysis</topic><topic>Other diseases. Semiology</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trépo, Eric</creatorcontrib><creatorcontrib>Potthoff, Andrej</creatorcontrib><creatorcontrib>Pradat, Pierre</creatorcontrib><creatorcontrib>Bakshi, Rakesh</creatorcontrib><creatorcontrib>Young, Bradford</creatorcontrib><creatorcontrib>Lagier, Robert</creatorcontrib><creatorcontrib>Moreno, Christophe</creatorcontrib><creatorcontrib>Verset, Laurine</creatorcontrib><creatorcontrib>Cross, Richard</creatorcontrib><creatorcontrib>Degré, Delphine</creatorcontrib><creatorcontrib>Lemmers, Arnaud</creatorcontrib><creatorcontrib>Gustot, Thierry</creatorcontrib><creatorcontrib>Berthillon, Pascale</creatorcontrib><creatorcontrib>Rosenberg, William</creatorcontrib><creatorcontrib>Trépo, Christian</creatorcontrib><creatorcontrib>Sninsky, John</creatorcontrib><creatorcontrib>Adler, Michael</creatorcontrib><creatorcontrib>Wedemeyer, Heiner</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trépo, Eric</au><au>Potthoff, Andrej</au><au>Pradat, Pierre</au><au>Bakshi, Rakesh</au><au>Young, Bradford</au><au>Lagier, Robert</au><au>Moreno, Christophe</au><au>Verset, Laurine</au><au>Cross, Richard</au><au>Degré, Delphine</au><au>Lemmers, Arnaud</au><au>Gustot, Thierry</au><au>Berthillon, Pascale</au><au>Rosenberg, William</au><au>Trépo, Christian</au><au>Sninsky, John</au><au>Adler, Michael</au><au>Wedemeyer, Heiner</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of a cirrhosis risk score for the early prediction of fibrosis progression in hepatitis C patients with minimal liver disease</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>55</volume><issue>1</issue><spage>38</spage><epage>44</epage><pages>38-44</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><coden>JOHEEC</coden><abstract>Background & Aims Fibrosis progression in patients with chronic hepatitis C (CHC) is highly variable. A Cirrhosis Risk Score (CRS) based on seven genetic variants has been recently developed for identifying patients at risk for cirrhosis. The objective of this study was to assess the role of the CRS for the early prediction of fibrosis progression in CHC patients with mild liver fibrosis. In addition, we evaluated the potential benefit, for prediction accuracy, of a recently described non-invasive fibrosis staging assay, the Enhanced Liver Fibrosis (ELF) test. Methods Two separate cohorts of HCV patients (Brussels, Belgium/Hannover, Germany) were retrospectively analyzed. Only patients with a fibrosis Ishak or METAVIR score of F0–F1 at baseline were included. Patients were classified as progressors if they showed an increase ⩾2 fibrosis stages at the second histological evaluation after a follow-up ⩾5 years. The CRS was calculated locally. Genotyping was performed by PCR and oligonucleotide ligation with the resulting signal detected with a Luminex® 200TM and computer analysis. Results In Brussels, 12/25 patients progressed (48%); similarly in Hannover, 16/31 (52%) patients progressed. In both sample sets, the CRS was significantly associated with fibrosis progression ( p = 0.050 in Brussels; p = 0.018 in Hannover). The ELF test was only a significant predictor in Hannover ( p = 0.015). In multivariate analysis the CRS remained the only variable associated with fibrosis progression (odds-ratio = 2.23, 95%CI 1.21–4.11 p = 0.01). Conclusions Although conducted on a limited number of patients, this study in two independent centres confirms that the CRS predicts fibrosis progression in initially mild CHC.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>21145859</pmid><doi>10.1016/j.jhep.2010.10.018</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Cirrhosis risk score (CRS) Cohort Studies Disease Progression Female Fibrosis progression Gastroenterology and Hepatology Gastroenterology. Liver. Pancreas. Abdomen Genetic Variation Hepatitis C Hepatitis C, Chronic - classification Hepatitis C, Chronic - complications Hepatitis C, Chronic - genetics Hepatitis C, Chronic - pathology Human viral diseases Humans Infectious diseases Liver Cirrhosis - classification Liver Cirrhosis - etiology Liver Cirrhosis - genetics Liver Cirrhosis - pathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Middle Aged Minimal liver disease Multivariate Analysis Other diseases. Semiology Polymorphism, Single Nucleotide Retrospective Studies Risk Factors Viral diseases Viral hepatitis |
title | Role of a cirrhosis risk score for the early prediction of fibrosis progression in hepatitis C patients with minimal liver disease |
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