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TREATMENT AND OUTCOMES OF RHEUMATOID ARTHRITIS PATIENTS WITH HEPATITIS B

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dc.contributor.authorChoi, C. -B.-
dc.contributor.authorSung, Y. -K.-
dc.contributor.authorCho, S. -K.-
dc.contributor.authorYoo, D. -H.-
dc.contributor.authorLee, S. -S.-
dc.contributor.authorLee, J.-
dc.contributor.authorKim, J.-
dc.contributor.authorLee, H. -S.-
dc.contributor.authorKim, T. -H.-
dc.contributor.authorYoon, B. Y.-
dc.contributor.authorYoo, W. -H.-
dc.contributor.authorChoe, J. -Y.-
dc.contributor.authorLee, S. -H.-
dc.contributor.authorShim, S. -C.-
dc.contributor.authorChung, W. -T.-
dc.contributor.authorHong, S. -J.-
dc.contributor.authorLee, C. K.-
dc.contributor.authorKoh, E.-
dc.contributor.authorJun, J. -B.-
dc.contributor.authorBang, S. -Y.-
dc.contributor.authorKim, S. -K.-
dc.contributor.authorCha, H. -S.-
dc.contributor.authorWon, S.-
dc.contributor.authorBae, S. -C.-
dc.date.accessioned2021-08-02T18:56:19Z-
dc.date.available2021-08-02T18:56:19Z-
dc.date.issued2013-06-
dc.identifier.issn0003-4967-
dc.identifier.issn1468-2060-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/26714-
dc.description.abstractBackground Treatment of rheumatoid arthritis (RA) patients with hepatitis B carries risk for reactivation of hepatitis B and drug-related hepatotoxicity. Objectives We investigated the impact of treatment for RA in patients with hepatitis B. Methods Patients enrolled in KORONA (Korean Observational Study Network for Arthritis) with 1-year follow up assessment with data on hepatitis B surface antigen (HBsAg) and hepatitis B core antibody (HBcAb) status were included in the analysis. Patient characteristics (age, sex, disease duration, delay in diagnosis, alcohol intake), disease outcome measures (DAS28, fatigue, sleep, HAQ, EQ-5D, radiographic damage, surgery), medications, and adverse events were assessed. Multiple logistic regression was used to analyze the predicting factors for liver function abnormalities. Results : A total of 871 patients were assessed. The number of HBsAg-positive and HBcAb-positive patients were 48 (5.5%) and 372 (42.7%), respectively. HBcAb-positive groups were significantly older (56.3 ± 10.8 vs 52.5 ± 9.0 in HBsAg-positive group and 51.3 ± 13.3 in negative group, p<0.01) and had longer disease duration (8.4 ± 7.7 vs 7.7 ± 6.0 in HBsAg-positive group and 7.8 ± 7.2 in negative-group, p=0.46). There was no significant difference in disease outcome measures between the groups, except for significantly increased radiographic damage in HBcAb group (79.6% vs 70.8% in HBsAg-positive group and 72.5% in negative group, p=0.048). Methotrexate and biologics use were significantly lower in HBsAg-positive group, while hydroxychloroquine, sulfasalazine, tacrolimus, and steroids use were significantly higher. HBsAg-positive group had significantly more adverse events (52.1%) compared to HBcAb-positive group (29.3%) and negative group (32.8%). HBsAg-positivity and HBcAb-positivity was not associated with significant increase in liver function abnormalities in the study population in multiple logistic regression analysis (OR (95%CI), 2.2 (0.7-7.4) and 0.8 (0.4-1.7), respectively). Conclusions HBsAg-positive patients were more frequently treated with steroids and less with methotrexate, but there was no significant difference in disease outcome. HBsAg-positive patients had more adverse events, but it did not show significant association with developing liver function abnormality.-
dc.language영어-
dc.language.isoENG-
dc.publisherBMJ Publishing Group-
dc.titleTREATMENT AND OUTCOMES OF RHEUMATOID ARTHRITIS PATIENTS WITH HEPATITIS B-
dc.title.alternativeTreatment and outcomes of rheumatoid arthritis patients with hepatitis b-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1136/annrheumdis-2013-eular.2536-
dc.identifier.wosid000331587904631-
dc.identifier.bibliographicCitationAnnals of the Rheumatic Diseases, v.72, no.suppl.3, pp A851.4 - A852-
dc.citation.titleAnnals of the Rheumatic Diseases-
dc.citation.volume72-
dc.citation.numbersuppl.3-
dc.citation.startPageA851.4-
dc.citation.endPageA852-
dc.type.docTypeMeeting Abstract-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaRheumatology-
dc.relation.journalWebOfScienceCategoryRheumatology-
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