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Levels of hepatitis B virus (HBV) replication during the nonreplicative phase: HBV quantification by real-time PCR in Korea

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dc.contributor.authorYim, Hyung Joon-
dc.contributor.authorByun, Kwan Soo-
dc.contributor.authorChang, Yun Jung-
dc.contributor.authorSuh, Yeon Seok-
dc.contributor.authorYeon, Jong Eun-
dc.contributor.authorLee, Chang Hong-
dc.contributor.authorKwon, Jung Ah-
dc.contributor.authorYoo, Wangdon-
dc.contributor.authorKim, Soo-Ok-
dc.contributor.authorHong, Sun Pyo-
dc.date.available2020-11-03T11:49:22Z-
dc.date.issued2007-09-
dc.identifier.issn0163-2116-
dc.identifier.issn1573-2568-
dc.identifier.urihttps://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/17781-
dc.description.abstractThe levels of HBV replication in the nonreplicative phase are not clear. We conducted this study to evaluate the levels of viral replication during the nonreplicative phase in chronic HBV-infected Korean patients using real-time PCR. A total of 125 patients were classified into three groups: inactive HBsAg carriers, inactive liver cirrhosis patients, and resolved chronic HBV-infected patients with loss of HBsAg. The real-time PCR detected HBV DNA in 112 cases (89.6%). The mean levels of HBV DNA were 3.84, 4.10, and 3.31 log copies/ml in the three groups, respectively (P < 0.01). Ninety-five percent of inactive HBsAg carriers showed levels of HBV DNA lower than 6x10(4) copies/ml. In conclusion, we showed different levels of HBV DNA exactly in three groups during nonreplicative phases. We suggest that the cutoff level of HBV DNA in inactive HBsAg carriers should be readjusted to a lower level in future studies.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherKluwer Academic/Plenum Publishers-
dc.titleLevels of hepatitis B virus (HBV) replication during the nonreplicative phase: HBV quantification by real-time PCR in Korea-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1007/s10620-006-9140-2-
dc.identifier.scopusid2-s2.0-34547843613-
dc.identifier.wosid000248810300062-
dc.identifier.bibliographicCitationDigestive Diseases and Sciences, v.52, no.9, pp 2403 - 2409-
dc.citation.titleDigestive Diseases and Sciences-
dc.citation.volume52-
dc.citation.number9-
dc.citation.startPage2403-
dc.citation.endPage2409-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusSURFACE-ANTIGEN-
dc.subject.keywordPlusHBSAG SEROCLEARANCE-
dc.subject.keywordPlusNATURAL-HISTORY-
dc.subject.keywordPlusDNA LEVELS-
dc.subject.keywordPlusINFECTION-
dc.subject.keywordPlusGENOTYPES-
dc.subject.keywordPlusMUTANT-
dc.subject.keywordPlusLIVER-
dc.subject.keywordPlusSERUM-
dc.subject.keywordPlusQUANTITATION-
dc.subject.keywordAuthornonreplicative phase-
dc.subject.keywordAuthorinactive HBsAg carriers-
dc.subject.keywordAuthorHBsAg loss-
dc.subject.keywordAuthorhepatitis B virus DNA-
dc.subject.keywordAuthorreal-time PCR-
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Guro Hospital (Department of Gastroenterology and Hepatology, Guro Hospital)
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