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Relationship of serum fibrosis markers with liver fibrosis stage and collagen content in patients with advanced chronic hepatitis C

dc.contributor.authorFontana, Robert Johnen_US
dc.contributor.authorGoodman, Zachary D.en_US
dc.contributor.authorDienstag, Jules L.en_US
dc.contributor.authorBonkovsky, Herbert L.en_US
dc.contributor.authorNaishadham, Deepaen_US
dc.contributor.authorSterling, Richard K.en_US
dc.contributor.authorSu, Grace L.en_US
dc.contributor.authorGhosh, Mitaen_US
dc.contributor.authorWright, Elizabeth C.en_US
dc.date.accessioned2008-03-06T19:10:08Z
dc.date.available2009-03-04T14:20:46Zen_US
dc.date.issued2008-03en_US
dc.identifier.citationFontana, Robert J.; Goodman, Zachary D.; Dienstag, Jules L.; Bonkovsky, Herbert L.; Naishadham, Deepa; Sterling, Richard K.; Su, Grace L.; Ghosh, Mita; Wright, Elizabeth C. (2008). "Relationship of serum fibrosis markers with liver fibrosis stage and collagen content in patients with advanced chronic hepatitis C Potential conflict of interest: Financial relationships of the authors with Hoffmann-La Roche Inc., are as follows: R.J. Fontana is on the speaker's bureau; R.K. Sterling is a consultant and on the speaker's bureau; Authors with no financial relationships related to this project are: Z.D. Goodman, J.L. Dienstag, D. Naishadham, Grace Su, Mita Ghosh, H.L. Bonkovsky, and E.C. Wright. ." Hepatology 47(3): 789-798. <http://hdl.handle.net/2027.42/58027>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/58027
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18175357&dopt=citation
dc.description.abstractThis study determined the utility of a panel of serum fibrosis markers along with routine laboratory tests in estimating the likelihood of histological cirrhosis in a cohort of prior nonresponders with chronic hepatitis C. The relationship between serum markers and quantitative hepatic collagen content was also determined. Liver biopsy samples from 513 subjects enrolled in the HALT-C trial were assigned Ishak fibrosis scores. The collagen content of 386 sirius-red stained, nonfragmented biopsy samples was quantified using computerized morphometry. Serum tissue inhibitor of matrix metalloproteinase-1 (TIMP-1), amino-terminal peptide of type III procollagen (PIIINP), hyaluronic acid (HA), and YKL-40 levels were determined using commercially available assays.Sixty-two percent of patients had noncirrhotic fibrosis (Ishak stage 2-4) whereas 38% had cirrhosis (Ishak stage 5,6). Multivariate analysis identified a 3-variable model (HA, TIMP-1, and platelet count) that had an area under the receiver operating curve (AUROC) of 0.81 for estimating the presence of cirrhosis. This model was significantly better than that derived from the cirrhosis discriminant score (AUROC 0.70), the AST-to-platelet ratio (AUROC 0.73), and a prior model developed in HALT-C patients (AUROC 0.79). Multivariate analysis demonstrated that the serum fibrosis markers correlated substantially better with Ishak fibrosis scores than with the log hepatic collagen content (AUROC 0.84 versus 0.72). Conclusion: A 3-variable model consisting of serum HA, TIMP-1, and platelet count was better than other published models in identifying cirrhosis in HALT-C Trial subjects. The stronger correlation of the serum markers with Ishak scores suggests that serum fibrosis markers reflect the pattern of fibrosis more closely than the quantity of hepatic collagen. (H EPATOLOGY 2008.)en_US
dc.format.extent263286 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherHepatologyen_US
dc.titleRelationship of serum fibrosis markers with liver fibrosis stage and collagen content in patients with advanced 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.affiliationumDepartment of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI ; fax: 734-936-7392 ; Department of Internal Medicine, University of Michigan Medical School, 3912 Taubman Center, Ann Arbor, MI 48109-0362en_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan Medical School, Ann Arbor, MIen_US
dc.contributor.affiliationotherArmed Forces Institute of Pathology, Washington, DCen_US
dc.contributor.affiliationotherGastrointestinal Unit, Medical Services, Massachusetts General Hospital, and the Department of Medicine, Harvard Medical School, Boston, MAen_US
dc.contributor.affiliationotherDepartments of Medicine and Molecular and Structural Biology and The Liver-Biliary-Pancreatic Center, University of Connecticut Health Center, Farmington, CTen_US
dc.contributor.affiliationotherNew England Research Institutes, Watertown, MAen_US
dc.contributor.affiliationotherHepatology Section, Virginia Commonwealth University Health System, Richmond, VAen_US
dc.contributor.affiliationotherAnn Arbor Veteran's Administration Health Center, Ann Arbor, MIen_US
dc.contributor.affiliationotherOffice of the Director, National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, MDen_US
dc.identifier.pmid18175357
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/58027/1/22099_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/hep.22099en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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