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Prevalence of HBV precore/core promoter variants in the United States

dc.contributor.authorChu, Chi-Jenen_US
dc.contributor.authorKeeffe, Emmet B.en_US
dc.contributor.authorHan, Steven-Huy B.en_US
dc.contributor.authorPerrillo, Robert P.en_US
dc.contributor.authorMin, Albert D.en_US
dc.contributor.authorSoldevila-Pico, Consueloen_US
dc.contributor.authorCarey, Williamen_US
dc.contributor.authorBrown, Robert S.en_US
dc.contributor.authorLuketic, Velimir A.en_US
dc.contributor.authorTerrault, Norah A.en_US
dc.contributor.authorLok, Anna Suk-Fongen_US
dc.date.accessioned2006-04-19T13:51:05Z
dc.date.available2006-04-19T13:51:05Z
dc.date.issued2003-09en_US
dc.identifier.citationChu, Chi-Jen; Keeffe, Emmet B.; Han, Steven-Huy; Perrillo, Robert P.; Min, Albert D.; Soldevila-Pico, Consuelo; Carey, William; Brown, Robert S.; Luketic, Velimir A.; Terrault, Norah; Lok, Anna S. F. (2003)."Prevalence of HBV precore/core promoter variants in the United States." Hepatology 38(3): 619-628. <http://hdl.handle.net/2027.42/34795>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34795
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12939588&dopt=citationen_US
dc.description.abstractVariants in the precore (G 1896 A) and core promoter (A 1762 T, G 1764 A) regions of hepatitis B virus (HBV) may be related to serum HBV DNA levels and severity of liver disease. The aims of this nationwide study were to determine the prevalence of HBV precore/core promoter variants in the United States and the association between these variants and patient demographics, HBV genotypes, serum HBV DNA level, and severity of liver disease. A total of 694 consecutive chronic HBV-infected patients seen in 17 U.S. liver centers during a 1-year period were enrolled. Demographic, clinical, and laboratory data were collected. Sera were tested for HBV genotypes as well as precore and core promoter variants by line-probe assays. Quantitative HBV DNA levels were determined using Cobas Amplicor HBV Monitor kits. Precore and core promoter variants were found in 27% and 44% of patients with chronic HBV infection in the United States. Precore and core promoter variants were more common in hepatitis B e antigen (HBeAg)-negative than in HBeAg-positive patients (precore, 38% vs. 9%; core promoter, 51% vs. 36%; respectively, P < .001). The prevalence of these variants was related to ethnicity, place of birth, and HBV genotypes. Patients with core promoter variants were more likely to have hepatic decompensation. Precore and/or core promoter variants were associated with higher serum HBV DNA levels in HBeAg-negative but not in HBeAg-positive patients. In conclusion, HBV precore and core promoter variants are not rare in the United States. Physicians should be aware of the existence of HBV precore and core promoter variants and the clinical condition of “HBeAg-negative chronic hepatitis.”en_US
dc.format.extent244527 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.titlePrevalence of HBV precore/core promoter variants in the United Statesen_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, Ann Arbor, MIen_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan, 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.contributor.affiliationotherStanford University, Stanford, CAen_US
dc.contributor.affiliationotherUniversity of California, Los Angeles, Los Angeles, CAen_US
dc.contributor.affiliationotherOchsner Clinic, New York, NYen_US
dc.contributor.affiliationotherMount Sinai School of Medicine, New York, NYen_US
dc.contributor.affiliationotherUniversity of Florida, Gainesville, FLen_US
dc.contributor.affiliationotherCleveland Clinic, Cleveland, OHen_US
dc.contributor.affiliationotherColumbia-Presbyterian Medical Center, New York, NYen_US
dc.contributor.affiliationotherVirginia Commonwealth University, Richmond, VAen_US
dc.contributor.affiliationotherUniversity of California, San Francisco, San Francisco, CAen_US
dc.identifier.pmid12939588en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34795/1/510380312_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1053/jhep.2003.50352en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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