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

被引:31
作者
Park, Kyoung Sook [1 ]
Han, Seung Hyeok [1 ]
Kie, Jeong Hae [2 ]
Nam, Ki Heon [1 ]
Lee, Mi Jung [1 ]
Lim, Beom Jin [3 ]
Kwon, Young Eun [1 ]
Kim, Yung Ly [1 ]
An, Seong Yeong [1 ]
Kim, Chan Ho [1 ]
Doh, Fa Mee [1 ]
Koo, Hyang Mo [1 ]
Oh, Hyung Jung [1 ]
Kang, Shin-Wook [1 ,4 ]
Choi, Kyu Hun [1 ]
Jeong, Hyeon Joo [3 ]
Yoo, Tae-Hyun [1 ]
机构
[1] Yonsei Univ, Coll Med, Dept Internal Med, Div Nephrol, Seoul 120752, South Korea
[2] NHIS Ilsan Hosp, Dept Pathol, Goyang Shi, Gyeonggi Do, South Korea
[3] Yonsei Univ, Coll Med, Dept Pathol, Seoul 120752, South Korea
[4] Yonsei Univ, Severance Biomed Sci Inst, Seoul 120752, South Korea
关键词
Proteinuria; IgA nephropathy; Long-term outcome; IMMUNOGLOBULIN-A NEPHROPATHY; CLINICOPATHOLOGICAL CORRELATIONS; PROGNOSTIC-FACTORS; NATURAL-HISTORY; KOREAN ADULTS; VALIDATION; PROGRESSION; DISEASE;
D O I
10.1016/j.humpath.2013.08.019
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:236 / 243
页数:8
相关论文
共 28 条
  • [1] The Use of the Oxford Classification of IgA Nephropathy to Predict Renal Survival
    Alamartine, Eric
    Sauron, Catherine
    Laurent, Blandine
    Sury, Aurore
    Seffert, Aline
    Mariat, Christophe
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 6 (10): : 2384 - 2388
  • [2] Risk Stratification of Patients With IgA Nephropathy
    Barbour, Sean J.
    Reich, Heather N.
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2012, 59 (06) : 865 - 873
  • [3] IgA nephropathy
    Barratt, J
    Feehally, J
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (07): : 2088 - 2097
  • [4] Predicting progression in IgA nephropathy
    Bartosik, LP
    Lajoie, G
    Sugar, L
    Cattran, DC
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (04) : 728 - 735
  • [5] Validation of some pathophysiological mechanisms of the CKD progression theory and outcome prediction in IgA nephropathy
    Bazzi, Claudio
    Rizza, Virginia
    Casellato, Daniela
    Stivali, Gilda
    Rachele, Gregorio
    Napodano, Pietro
    Olivieri, Giulia
    Gallieni, Maurizio
    D'Amico, Giuseppe
    [J]. JOURNAL OF NEPHROLOGY, 2012, 25 (05) : 810 - 818
  • [6] The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification
    Cattran, Daniel C.
    Coppo, Rosanna
    Cook, H. Terence
    Feehally, John
    Roberts, Ian S. D.
    Troyanov, Stephan
    Alpers, Charles E.
    Amore, Alessandro
    Barratt, Jonathan
    Berthoux, Francois
    Bonsib, Stephen
    Bruijn, Jan A.
    D'Agati, Vivette
    D'Amico, Giuseppe
    Emancipator, Steven
    Emma, Francesco
    Ferrario, Franco
    Fervenza, Fernando C.
    Florquin, Sandrine
    Fogo, Agnes
    Geddes, Colin C.
    Groene, Hermann-Josef
    Haas, Mark
    Herzenberg, Andrew M.
    Hill, Prue A.
    Hogg, Ronald J.
    Hsu, Stephen I.
    Jennette, J. Charles
    Joh, Kensuke
    Julian, Bruce A.
    Kawamura, Tetsuya
    Lai, Fernand M.
    Leung, Chi Bon
    Li, Lei-Shi
    Li, Philip K. T.
    Liu, Zhi-Hong
    Mackinnon, Bruce
    Mezzano, Sergio
    Schena, F. Paolo
    Tomino, Yasuhiko
    Walker, Patrick D.
    Wang, Haiyan
    Weening, Jan J.
    Yoshikawa, Nori
    Zhang, Hong
    [J]. KIDNEY INTERNATIONAL, 2009, 76 (05) : 534 - 545
  • [8] Coppo R, 2010, Prilozi, V31, P241
  • [9] Natural history of idiopathic IgA nephropathy: Role of clinical and histological prognostic factors
    D'Amico, G
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 36 (02) : 227 - 237
  • [10] DONADIO JV, 1994, CLIN NEPHROL, V41, P65