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Analysis of rheumatoid factor according to various hepatitis B virus infectious statuses

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dc.contributor.author박용범-
dc.contributor.author이수곤-
dc.date.accessioned2015-12-28T11:09:23Z-
dc.date.available2015-12-28T11:09:23Z-
dc.date.issued2014-
dc.identifier.issn0392-856X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/138816-
dc.description.abstractOBJECTIVES: Rheumatoid factor (RF) can be seen in hepatitis B virus (HBV) infection. We investigated RF positive rates according to various HBV infectious statuses and vaccination, and the relationship between RF titers and serum HBV DNA levels. METHODS: We examined 13,670 individuals who visited the Severance Hospital in Seoul, Korea, for a routine health check-up, and obtained serum samples from all individuals. RESULTS: RF was positive in 3.5% of all subjects, and HBsAg was positive in 4.3%. HBsAg was positive in 21.7% of all RF positive subjects. RF was positive in 17.5% of the HBsAg positive group, while it was positive in 2.9% of the HBsAg negative group (p<0.001). The RF positive rate was increased in positive HBsAg, female sex, and older age. The RF positive rate was lower in those who had anti-HBs after HBV vaccination than in HBsAg positive subjects (2.7% vs. 17.5%, p<0.001). Among the RF positive patients, the RF titer in HBsAg positive patients were higher than that in HBsAg negative patients (159.7±217.1IU/mL vs. 83.0±179.2 IU/mL, p=0.001). The load of HBV DNA may be closely correlated with RF titer in patients with chronic hepatitis B (r=0.508, p=0.005). CONCLUSIONS: Persistent HBV infection is an important cause for the positive RF in HBV endemic areas. Hepatitis B viral load is associated with RF titer. HBV vaccination may reduce the risk of RF formation.-
dc.description.statementOfResponsibilityopen-
dc.format.extent168~173-
dc.relation.isPartOfCLINICAL AND EXPERIMENTAL RHEUMATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAge Factors-
dc.subject.MESHDNA, Viral/blood*-
dc.subject.MESHFemale-
dc.subject.MESHHepatitis B*/epidemiology-
dc.subject.MESHHepatitis B*/immunology-
dc.subject.MESHHepatitis B*/physiopathology-
dc.subject.MESHHepatitis B Antibodies/blood-
dc.subject.MESHHepatitis B Surface Antigens/blood-
dc.subject.MESHHepatitis B virus*/genetics-
dc.subject.MESHHepatitis B virus*/immunology-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPatient Acuity-
dc.subject.MESHRepublic of Korea/epidemiology-
dc.subject.MESHRheumatoid Factor*/analysis-
dc.subject.MESHRheumatoid Factor*/blood-
dc.subject.MESHSex Factors-
dc.subject.MESHStatistics as Topic-
dc.subject.MESHViral Load-
dc.titleAnalysis of rheumatoid factor according to various hepatitis B virus infectious statuses-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorS T Choi-
dc.contributor.googleauthorH W Lee-
dc.contributor.googleauthorJ S Song-
dc.contributor.googleauthorS K Lee-
dc.contributor.googleauthorY B Park-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01579-
dc.contributor.localIdA02889-
dc.relation.journalcodeJ00555-
dc.identifier.eissn1593-098X-
dc.identifier.pmid24143967-
dc.identifier.urlhttp://www.clinexprheumatol.org/abstract.asp?a=7153-
dc.contributor.alternativeNamePark, Yong Beom-
dc.contributor.alternativeNameLee, Soo Kon-
dc.contributor.affiliatedAuthorPark, Yong Beom-
dc.contributor.affiliatedAuthorLee, Soo Kon-
dc.rights.accessRightsfree-
dc.citation.volume32-
dc.citation.number2-
dc.citation.startPage168-
dc.citation.endPage173-
dc.identifier.bibliographicCitationCLINICAL AND EXPERIMENTAL RHEUMATOLOGY, Vol.32(2) : 168-173, 2014-
dc.identifier.rimsid54939-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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