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Iron reduction before and during interferon therapy of chronic hepatitis C: Results of a multicenter, randomized, controlled trial

dc.contributor.authorFontana, Robert Johnen_US
dc.contributor.authorIsrael, Jonathanen_US
dc.contributor.authorLeClair, Paulaen_US
dc.contributor.authorBanner, Barbara F.en_US
dc.contributor.authorTortorelli, Kristinaen_US
dc.contributor.authorGrace, Normanen_US
dc.contributor.authorLevine, Robert A.en_US
dc.contributor.authorFiarman, Galeen_US
dc.contributor.authorThiim, Michaelen_US
dc.contributor.authorTavill, Anthony S.en_US
dc.contributor.authorBonkovsky, Herbert L.en_US
dc.date.accessioned2006-04-19T13:49:56Z
dc.date.available2006-04-19T13:49:56Z
dc.date.issued2000-03en_US
dc.identifier.citationFontana, Robert J.; Israel, Jonathan; LeClair, Paula; Banner, Barbara F.; Tortorelli, Kristina; Grace, Norman; Levine, Robert A.; Fiarman, Gale; Thiim, Michael; Tavill, Anthony S.; Bonkovsky, Herbert L. (2000)."Iron reduction before and during interferon therapy of chronic hepatitis C: Results of a multicenter, randomized, controlled trial." Hepatology 31(3): 730-736. <http://hdl.handle.net/2027.42/34777>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34777
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10706565&dopt=citationen_US
dc.description.abstractPatients with chronic hepatitis C and low serum and hepatic iron stores may have an improved response to interferon (IFN). We tested whether iron reduction before and during IFN therapy would lead to an improved sustained biochemical and virological response compared with IFN alone. Eighty-two previously untreated patients with chronic hepatitis C were randomized to either: group A IFN-Α2b 3 MU 3 times per week for 6 months, or group B iron reduction before and during IFN-Α2b 3 MU 3 times per week for 6 months. Group B patients had lower mean serum alanine transaminase (ALT) levels than group A patients during treatment and follow-up. Group B patients had significantly lower mean hepatitis C virus (HCV)-RNA levels at treatment weeks 4 and 12 ( P < .05). Serum HCV RNA was undetectable at the end of treatment in 15 group B patients compared with 7 group A patients ( P = .03); 7 group B patients and 3 group A patients had persistently undetectable serum HCV RNA 24 weeks after the end of therapy ( P = .20). Paired pre- and posttreatment liver biopsies in 18 group B patients demonstrated significant improvements in 2 of the 3 inflammation scores of the Knodell histological activity index ( P < .05). No changes occurred in the paired biopsies from 15 group A patients. We conclude that iron reduction via therapeutic phlebotomy improves the end-of-treatment virological and histological response to short-term IFN therapy. Additional studies are needed to determine if iron reduction in combination with higher doses or longer duration of IFN may be of benefit.en_US
dc.format.extent128680 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.titleIron reduction before and during interferon therapy of chronic hepatitis C: Results of a multicenter, randomized, controlled trialen_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.affiliationumUniversity of Michigan Medical School, Ann Arbor, MIen_US
dc.contributor.affiliationumState University of New York Health Sciences Center at Syracuse, NY ; Division of Gastroenterology, University of Michigan Medical School, 3912 Taubman Center, Box 0362, Ann Arbor, MI 48109. fax: (734) 936-7392en_US
dc.contributor.affiliationotherHartford Hospital and University of Connecticut School of Medicine, Hartford, CTen_US
dc.contributor.affiliationotherUniversity of Massachusetts Medical School and U. Mass Memorial Health Care, Worcester, MAen_US
dc.contributor.affiliationotherUniversity of Massachusetts Medical School and U. Mass Memorial Health Care, Worcester, MAen_US
dc.contributor.affiliationotherUniversity of Massachusetts Medical School and U. Mass Memorial Health Care, Worcester, MAen_US
dc.contributor.affiliationotherFaulkner Hospital and Tufts University School of Medicine, Boston, MAen_US
dc.contributor.affiliationotherLahey Clinic, Burlington, MAen_US
dc.contributor.affiliationotherLahey Clinic, Burlington, MAen_US
dc.contributor.affiliationotherMt. Sinai Medical Center and Case Western Reserve University, Cleveland, OHen_US
dc.contributor.affiliationotherUniversity of Massachusetts Medical School and U. Mass Memorial Health Care, Worcester, MAen_US
dc.identifier.pmid10706565en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34777/1/510310325_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/hep.510310325en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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