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Prognostic value of chronicity grading on renal outcomes in patients with IgA nephropathyopen access

Authors
Kang, DonghyukBan, Tae HyunChin, Ho JunLee, HajeongOh, Se WonPark, Cheol WheeYang, Chul WooChoi, Bum SoonKorean GlomeruloNEphritis sTudy groupKwon, Young JooAhn, Shin Young
Issue Date
Aug-2022
Publisher
Frontiers Media S.A.
Keywords
IgA nephropathy; end-stage renal disease; renal biopsy; pathology; glomerulosclerosis; interstitial fibrosis
Citation
Frontiers in Medicine, v.9
Indexed
SCIE
SCOPUS
Journal Title
Frontiers in Medicine
Volume
9
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/61510
DOI
10.3389/fmed.2022.952050
ISSN
2296-858X
2296-858X
Abstract
Many studies have shown that chronic changes are strong predictors of renal outcomes in various kidney diseases, including IgA nephropathy. The Mayo Clinic/Renal Pathology Society suggested a glomerulonephritis reporting system with a proposal for standardized grading of chronic changes. The purpose of this study was to predict renal outcomes in patients with IgA nephropathy using chronicity grading in comparison to the Oxford classification which did not include global sclerosis. A total of 4,151 patients with IgA nephropathy were enrolled from the Korean GlomeruloNephritis Study Group registry. Chronicity grading was categorized into minimal, mild, moderate, and severe according to the extent of chronic changes. The Oxford T and S scores were considered as chronic lesions. Three prediction models were constructed: the Oxford classification model (Oxford S plus T), chronicity grading model A (chronicity grading), and chronicity grading model B (chronicity grading plus Oxford S). Using these three prediction models, the primary renal outcome (end-stage renal disease) was evaluated using Cox regression analysis and prediction performance. During the median follow-up of 6.1 (2.7-9.9) years, 304 (7.3%) patients progressed to end-stage renal disease with a cumulative incidence rate of 1.02 events per 100 person-years. In a fully adjusted multivariable model, chronicity grading was independently associated with the primary renal outcome in both models A and B. Compared to the Oxford model, both models A and B showed improvements in model fit, but not in discrimination (Delta C 0.001; 95% CI, -0.010 to 0.013 and Delta C 0.002; 95% CI, -0.005 to 0.008, respectively). Model B demonstrated improvements in integrated discrimination improvement (0.01; 95% CI, 0-0.03) and continuous net reclassification improvement (0.49; 95% CI, 0.02-0.72). The severity of chronicity grading is closely related to adverse renal outcomes in patients with IgA nephropathy, and chronicity grading could provide additional information in clinical practice alongside the Oxford classification.
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Kwon, Young Joo
Guro Hospital (Department of Nephrology and Hypertension, Guro Hospital)
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