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

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dc.contributor.authorPark, Kyoung Sook-
dc.contributor.authorHan, Seung Hyeok-
dc.contributor.authorKie, Jeong Hae-
dc.contributor.authorNam, Ki Heon-
dc.contributor.authorLee, Mi Jung-
dc.contributor.authorLim, Beom Jin-
dc.contributor.authorKwon, Young Eun-
dc.contributor.authorKim, Yung Ly-
dc.contributor.authorAn, Seong Yeong-
dc.contributor.authorKim, Chan Ho-
dc.contributor.authorDoh, Fa Mee-
dc.contributor.authorKoo, Hyang Mo-
dc.contributor.authorOh, Hyung Jung-
dc.contributor.authorKang, Shin-Wook-
dc.contributor.authorChoi, Kyu Hun-
dc.contributor.authorChoi, Kyu Hun-
dc.contributor.authorYoo, Tae-Hyun-
dc.date.accessioned2022-07-16T06:01:52Z-
dc.date.available2022-07-16T06:01:52Z-
dc.date.created2021-05-13-
dc.date.issued2014-02-
dc.identifier.issn0046-8177-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/160624-
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.language영어-
dc.language.isoen-
dc.publisherW B SAUNDERS CO-ELSEVIER INC-
dc.titleComparison of the Haas and the Oxford classifications for prediction of renal outcome in patients with IgA nephropathy-
dc.typeArticle-
dc.contributor.affiliatedAuthorKwon, Young Eun-
dc.identifier.doi10.1016/j.humpath.2013.08.019-
dc.identifier.scopusid2-s2.0-84892687716-
dc.identifier.wosid000330551300006-
dc.identifier.bibliographicCitationHUMAN PATHOLOGY, v.45, no.2, pp.236 - 243-
dc.relation.isPartOfHUMAN PATHOLOGY-
dc.citation.titleHUMAN PATHOLOGY-
dc.citation.volume45-
dc.citation.number2-
dc.citation.startPage236-
dc.citation.endPage243-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPathology-
dc.relation.journalWebOfScienceCategoryPathology-
dc.subject.keywordPlusIMMUNOGLOBULIN-A NEPHROPATHY-
dc.subject.keywordPlusCLINICOPATHOLOGICAL CORRELATIONS-
dc.subject.keywordPlusPROGNOSTIC-FACTORS-
dc.subject.keywordPlusNATURAL-HISTORY-
dc.subject.keywordPlusKOREAN ADULTS-
dc.subject.keywordPlusVALIDATION-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordAuthorProteinuria-
dc.subject.keywordAuthorIgA nephropathy-
dc.subject.keywordAuthorLong-term outcome-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0046817713003766?via%3Dihub-
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