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The Impact of Inosine Triphosphatase Variants on Hemoglobin Level and Sustained Virologic Response of Chronic Hepatitis C in Korean

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dc.contributor.authorKim J.S.-
dc.contributor.authorAhn S.-M.-
dc.contributor.authorJung Y.K.-
dc.contributor.authorKwon Y.K.J.-
dc.contributor.authorKim Y.S.-
dc.contributor.authorChoi D.J.-
dc.contributor.authorKim J.H.-
dc.date.available2020-11-02T22:43:31Z-
dc.date.issued2013-
dc.identifier.issn1011-8934-
dc.identifier.issn1598-6357-
dc.identifier.urihttps://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/11352-
dc.description.abstractTwo variants of the inosine triphosphatase (ITPA: rs1127354, rs7270101) gene cause ITPA deficiency and protect against the hemolytic toxicity of ribavirin. We investigated the clinical significance of ITPA variants in Korean patients treated with pegylated interferon (PEG-IFN) plus ribavirin. Of the 133 patients, 108 were CC and 25 were non-CC at rs1127354 (groups A and B, respectively). On the other hand, at rs7270101 all 133 were AA. The mean values of Hemoglobin (Hgb) after 4, 8, and 12 weeks of treatment in groups A and B were 12.2 and 14.0, 11.8 and 13.2, and 11.5 and 12.9, respectively (P = 0.001, 0.036, 0.036). Sustained virologic response (SVR) was achieved in 67.8% (40/59) of genotype 1 patients and in 75% (27/36) of non-genotype 1 patients. Regarding ITPA variants, SVR was achieved by 66% and 80% of genotype 1 (P = 0.282), and by 78% and 71% (P = 0.726) of non-genotype 1. SVR was not significantly different in groups A and B. In conclusion, non-CC at rs1127354 without involvement of rs7270101 is strongly associated with protection from ribavirin-induced anemia, however, ITPA genotype is not associated with SVR. © 2013 The Korean Academy of Medical Sciences.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.titleThe Impact of Inosine Triphosphatase Variants on Hemoglobin Level and Sustained Virologic Response of Chronic Hepatitis C in Korean-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.3346/jkms.2013.28.8.1213-
dc.identifier.scopusid2-s2.0-84884364955-
dc.identifier.bibliographicCitationJournal of Korean Medical Science, v.28, no.8, pp 1213 - 1219-
dc.citation.titleJournal of Korean Medical Science-
dc.citation.volume28-
dc.citation.number8-
dc.citation.startPage1213-
dc.citation.endPage1219-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPlusalpha interferon-
dc.subject.keywordPlusantivirus agent-
dc.subject.keywordPlushemoglobin-
dc.subject.keywordPlusIL28B protein, human-
dc.subject.keywordPlusinorganic pyrophosphatase-
dc.subject.keywordPlusinosine triphosphatase-
dc.subject.keywordPlusinterleukin derivative-
dc.subject.keywordPlusmacrogol derivative-
dc.subject.keywordPluspeginterferon alpha2a-
dc.subject.keywordPlusrecombinant protein-
dc.subject.keywordPlusribavirin-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusallele-
dc.subject.keywordPlusanemia-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusAsian-
dc.subject.keywordPluscohort analysis-
dc.subject.keywordPlusdrug combination-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusgenetics-
dc.subject.keywordPlusgenotype-
dc.subject.keywordPlushemolysis-
dc.subject.keywordPlushepatitis C-
dc.subject.keywordPlusHepatitis C virus-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusIL28B-
dc.subject.keywordPlusITPA-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusmiddle aged-
dc.subject.keywordPlusretrospective study-
dc.subject.keywordPlusSouth Korea-
dc.subject.keywordPlustreatment outcome-
dc.subject.keywordPlusAnemia-
dc.subject.keywordPlusHepatitis C, Chronic-
dc.subject.keywordPlusIL28B-
dc.subject.keywordPlusITPA-
dc.subject.keywordPlusRibavirin-
dc.subject.keywordPlusAdult-
dc.subject.keywordPlusAlleles-
dc.subject.keywordPlusAntiviral Agents-
dc.subject.keywordPlusAsian Continental Ancestry Group-
dc.subject.keywordPlusCohort Studies-
dc.subject.keywordPlusDrug Therapy, Combination-
dc.subject.keywordPlusFemale-
dc.subject.keywordPlusGenotype-
dc.subject.keywordPlusHemoglobins-
dc.subject.keywordPlusHemolysis-
dc.subject.keywordPlusHepacivirus-
dc.subject.keywordPlusHepatitis C, Chronic-
dc.subject.keywordPlusHumans-
dc.subject.keywordPlusInterferon-alpha-
dc.subject.keywordPlusInterleukins-
dc.subject.keywordPlusMale-
dc.subject.keywordPlusMiddle Aged-
dc.subject.keywordPlusPolyethylene Glycols-
dc.subject.keywordPlusPyrophosphatases-
dc.subject.keywordPlusRecombinant Proteins-
dc.subject.keywordPlusRepublic of Korea-
dc.subject.keywordPlusRetrospective Studies-
dc.subject.keywordPlusRibavirin-
dc.subject.keywordPlusTreatment Outcome-
dc.subject.keywordAuthorAnemia-
dc.subject.keywordAuthorChronic-
dc.subject.keywordAuthorHepatitis C-
dc.subject.keywordAuthorIl28b-
dc.subject.keywordAuthorItpa-
dc.subject.keywordAuthorRibavirin-
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Ansan Hospital (Department of Gastroenterology and Hepatology, Ansan Hospital)
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