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Comparison of the Haas and the Oxford classifications for prediction of renal outcome in patients with IgA nephropathy.

DC Field Value Language
dc.contributor.author이미정-
dc.contributor.author임범진-
dc.contributor.author정현주-
dc.contributor.author최규헌-
dc.contributor.author강신욱-
dc.contributor.author한승혁-
dc.contributor.author구향모-
dc.contributor.author권영은-
dc.contributor.author김영리-
dc.contributor.author김찬호-
dc.contributor.author남기헌-
dc.contributor.author도화미-
dc.contributor.author박경숙-
dc.contributor.author안성영-
dc.contributor.author오형중-
dc.contributor.author유태현-
dc.date.accessioned2015-01-06T16:24:58Z-
dc.date.available2015-01-06T16:24:58Z-
dc.date.issued2014-
dc.identifier.issn0046-8177-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/98063-
dc.description.abstractPathologic features can provide valuable information for determining prognosis in IgA nephropathy (IgAN). However, it is uncertain whether the Oxford classification, a new classification of IgAN, can predict renal outcome better than previous ones. We conducted a retrospective cohort study in 500 patients with biopsy-proven IgAN between January 2002 and December 2010 to compare the ability of the Haas and the Oxford classifications to predict renal outcome. Primary outcome was a doubling of the baseline serum creatinine concentration (D-SCr). During a mean follow-up of 68 months, 52 (10.4%) and 35 (7.0%) developed D-SCr and end-stage renal disease, respectively. There were graded increases in the development of D-SCr in the higher Haas classes. In addition, the primary endpoint of D-SCr occurred more in patients with the Oxford M and T lesions than those without such lesions. In multivariate Cox regression analyses, the Haas class V (HR, 12.19; P=.002) and the Oxford T1 (hazard ratio [HR], 6.68; P<.001) and T2 (HR, 12.16; P<.001) lesions were independently associated with an increased risk of reaching D-SCr. Harrell's C index of each multivariate model with the Haas and the Oxford classification was 0.867 (P=.015) and 0.881 (P=.004), respectively. This was significantly higher than that of model with clinical factors only (C=0.819). However, there was no difference in C-statistics between the 2 models with the Haas and the Oxford classifications (P=.348). This study suggests that the Haas and the Oxford classifications are comparable in predicting progression of IgAN.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfHUMAN PATHOLOGY-
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.MESHCreatinine/blood-
dc.subject.MESHDisease Progression-
dc.subject.MESHFemale-
dc.subject.MESHGlomerulonephritis, IGA/classification*-
dc.subject.MESHGlomerulonephritis, IGA/complications*-
dc.subject.MESHGlomerulonephritis, IGA/pathology-
dc.subject.MESHHumans-
dc.subject.MESHKidney Failure, Chronic/etiology*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPrognosis-
dc.subject.MESHProportional Hazards Models-
dc.subject.MESHRetrospective Studies-
dc.titleComparison of the Haas and the Oxford classifications for prediction of renal outcome in patients with IgA nephropathy.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorKyoung Sook Park-
dc.contributor.googleauthorSeung Hyeok Han-
dc.contributor.googleauthorJeong Hae Kie-
dc.contributor.googleauthorKi Heon Nam-
dc.contributor.googleauthorMi Jung Lee-
dc.contributor.googleauthorBeom Jin Lim-
dc.contributor.googleauthorYoung Eun Kwon-
dc.contributor.googleauthorYung Ly Kim-
dc.contributor.googleauthorSeong Yeong An-
dc.contributor.googleauthorChan Ho Kim-
dc.contributor.googleauthorFa Mee Doh-
dc.contributor.googleauthorHyang Mo Koo-
dc.contributor.googleauthorHyung Jung Oh-
dc.contributor.googleauthorShin-Wook Kang-
dc.contributor.googleauthorKyu Hun Choi-
dc.contributor.googleauthorHyeon Joo Jeong-
dc.contributor.googleauthorTae-Hyun Yoo-
dc.identifier.doi10.1016/j.humpath.2013.08.019-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03363-
dc.contributor.localIdA03771-
dc.contributor.localIdA04043-
dc.contributor.localIdA00053-
dc.contributor.localIdA04304-
dc.contributor.localIdA00203-
dc.contributor.localIdA00232-
dc.contributor.localIdA00277-
dc.contributor.localIdA00703-
dc.contributor.localIdA01037-
dc.contributor.localIdA01244-
dc.contributor.localIdA01315-
dc.contributor.localIdA01423-
dc.contributor.localIdA02236-
dc.contributor.localIdA02417-
dc.contributor.localIdA02526-
dc.contributor.localIdA02773-
dc.relation.journalcodeJ01011-
dc.identifier.eissn1532-8392-
dc.identifier.pmid24439222-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0046817713003766-
dc.subject.keywordIgA nephropathy-
dc.subject.keywordLong-term outcome-
dc.subject.keywordProteinuria-
dc.contributor.alternativeNameLee, Mi Jung-
dc.contributor.alternativeNameLim, Beom Jin-
dc.contributor.alternativeNameJeong, Hyeon Joo-
dc.contributor.alternativeNameChoi, Kyu Hun-
dc.contributor.alternativeNameKang, Shin Wook-
dc.contributor.alternativeNameHan, Seung Hyeok-
dc.contributor.alternativeNameKoo, Hyang Mo-
dc.contributor.alternativeNameKwon, Young Eun-
dc.contributor.alternativeNameKie, Jeong Hae-
dc.contributor.alternativeNameKim, Yung Ly-
dc.contributor.alternativeNameKim, Chan Ho-
dc.contributor.alternativeNameNam, Ki Heon-
dc.contributor.alternativeNameDoh, Fa Mee-
dc.contributor.alternativeNamePark, Kyoung Sook-
dc.contributor.alternativeNameAn, Seong Yeong-
dc.contributor.alternativeNameOh, Hyung Jung-
dc.contributor.alternativeNameYoo, Tae Hyun-
dc.contributor.affiliatedAuthorLim, Beom Jin-
dc.contributor.affiliatedAuthorJeong, Hyeon Joo-
dc.contributor.affiliatedAuthorChoi, Kyu Hun-
dc.contributor.affiliatedAuthorKang, Shin Wook-
dc.contributor.affiliatedAuthorHan, Seung Hyeok-
dc.contributor.affiliatedAuthorKoo, Hyang Mo-
dc.contributor.affiliatedAuthorKwon, Young Eun-
dc.contributor.affiliatedAuthorKie, Jeong Hae-
dc.contributor.affiliatedAuthorKim, Yung Ly-
dc.contributor.affiliatedAuthorKim, Chan Ho-
dc.contributor.affiliatedAuthorNam, Ki Heon-
dc.contributor.affiliatedAuthorDoh, Fa Mee-
dc.contributor.affiliatedAuthorPark, Kyoung Sook-
dc.contributor.affiliatedAuthorAn, Seong Yeong-
dc.contributor.affiliatedAuthorOh, Hyung Jung-
dc.contributor.affiliatedAuthorYoo, Tae Hyun-
dc.contributor.affiliatedAuthorLee, Mi Jung-
dc.rights.accessRightsfree-
dc.citation.volume45-
dc.citation.number2-
dc.citation.startPage236-
dc.citation.endPage243-
dc.identifier.bibliographicCitationHUMAN PATHOLOGY, Vol.45(2) : 236-243, 2014-
dc.identifier.rimsid54363-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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