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A simple noninvasive index can predict both significant fibrosis and cirrhosis in patients with chronic hepatitis C

dc.contributor.authorWai, Chun-Taoen_US
dc.contributor.authorGreenson, Joel K.en_US
dc.contributor.authorFontana, Robert Johnen_US
dc.contributor.authorKalbfleisch, John D.en_US
dc.contributor.authorMarrero, Jorge A.en_US
dc.contributor.authorConjeevaram, Hari S.en_US
dc.contributor.authorLok, Anna Suk-Fongen_US
dc.date.accessioned2006-04-19T13:51:03Z
dc.date.available2006-04-19T13:51:03Z
dc.date.issued2003-08en_US
dc.identifier.citationWai, Chun-Tao; Greenson, Joel K.; Fontana, Robert J.; Kalbfleisch, John D.; Marrero, Jorge A.; Conjeevaram, Hari S.; Lok, Anna S.-F. (2003)."A simple noninvasive index can predict both significant fibrosis and cirrhosis in patients with chronic hepatitis C." Hepatology 38(2): 518-526. <http://hdl.handle.net/2027.42/34794>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34794
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12883497&dopt=citationen_US
dc.description.abstractInformation on the stage of liver fibrosis is essential in managing chronic hepatitis C (CHC) patients. However, most models for predicting liver fibrosis are complicated and separate formulas are needed to predict significant fibrosis and cirrhosis. The aim of our study was to construct one simple model consisting of routine laboratory data to predict both significant fibrosis and cirrhosis among patients with CHC. Consecutive treatment-naive CHC patients who underwent liver biopsy over a 25-month period were divided into 2 sequential cohorts: training set (n = 192) and validation set (n = 78). The best model for predicting both significant fibrosis (Ishak score ≥ 3) and cirrhosis in the training set included platelets, aspartate aminotransferase (AST), and alkaline phosphatase with an area under ROC curves (AUC) of 0.82 and 0.92, respectively. A novel index, AST to platelet ratio index (APRI), was developed to amplify the opposing effects of liver fibrosis on AST and platelet count. The AUC of APRI for predicting significant fibrosis and cirrhosis were 0.80 and 0.89, respectively, in the training set. Using optimized cut-off values, significant fibrosis could be predicted accurately in 51% and cirrhosis in 81% of patients. The AUC of APRI for predicting significant fibrosis and cirrhosis in the validation set were 0.88 and 0.94, respectively. In conclusion, our study showed that a simple index using readily available laboratory results can identify CHC patients with significant fibrosis and cirrhosis with a high degree of accuracy. Application of this index may decrease the need for staging liver biopsy specimens among CHC patients.en_US
dc.format.extent149836 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherW.B. Saundersen_US
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherHepatologyen_US
dc.titleA simple noninvasive index can predict both significant fibrosis and cirrhosis in patients with chronic hepatitis Cen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan Medical School, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MIen_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan Medical School, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Biostatistics, University of Michigan Medical School, Ann Arbor, MIen_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan Medical School, Ann Arbor, MIen_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan Medical School, Ann Arbor, MIen_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan Medical School, Ann Arbor, MI ; Division of Gastroenterology, University of Michigan Medical Center, 3912 Taubman Center, Box 0362, Ann Arbor, MI 48109-0362. fax: 734-936-7392en_US
dc.identifier.pmid12883497en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34794/1/510380230_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1053/jhep.2003.50346en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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