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

Authors
Park, Kyoung SookHan, Seung HyeokKie, Jeong HaeNam, Ki HeonLee, Mi JungLim, Beom JinKwon, Young EunKim, Yung LyAn, Seong YeongKim, Chan HoDoh, Fa MeeKoo, Hyang MoOh, Hyung JungKang, Shin-WookChoi, Kyu HunChoi, Kyu HunYoo, Tae-Hyun
Issue Date
Feb-2014
Publisher
W B SAUNDERS CO-ELSEVIER INC
Keywords
Proteinuria; IgA nephropathy; Long-term outcome
Citation
HUMAN PATHOLOGY, v.45, no.2, pp.236 - 243
Indexed
SCIE
SCOPUS
Journal Title
HUMAN PATHOLOGY
Volume
45
Number
2
Start Page
236
End Page
243
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/160624
DOI
10.1016/j.humpath.2013.08.019
ISSN
0046-8177
Abstract
Pathologic 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.
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