Related Experiment Video
Updated: May 16, 2026

Detection of MicroRNA Expression in the Kidneys of Immunoglobulin A Nephropathic Mice
Published on: July 8, 2020
Validation of the Oxford classification of IgA nephropathy for pediatric patients from China
Weibo Le1, Cai-Hong Zeng, Zhangsuo Liu
1Research Institute of Nephrology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China.
Insights
Tubular atrophy/interstitial fibrosis is the key predictor of kidney outcomes in children with IgA nephropathy (IgAN). This finding validates the Oxford classification
Area of Science:
- Nephrology
- Pediatric Nephrology
- Renal Pathology
Background:
- The Oxford classification aids in predicting IgA nephropathy (IgAN) prognosis.
- Validation in diverse pediatric populations is needed for the Oxford classification.
- IgA nephropathy is a common cause of glomerulonephritis in children.
Purpose of the Study:
- To evaluate the Oxford classification's utility in predicting renal outcomes in Chinese children with IgAN.
- To identify pathological predictors of renal function decline in pediatric IgAN.
Main Methods:
- Retrospective analysis of 218 children with IgAN from 7 Chinese renal centers.
- Inclusion criteria mirrored the original Oxford study.
- Median follow-up of 56 months to assess renal outcomes (ESRD or 50% GFR decline).
Main Results:
- Tubular atrophy/interstitial fibrosis (T1/T2) and segmental glomerulosclerosis (S1) were significant univariate predictors.
- Mesangial proliferation (M1), endocapillary proliferation (E1), and crescents were not significant predictors.
- Tubular atrophy/interstitial fibrosis remained the sole independent predictor in multivariate analysis (HR 2.9, P=0.04).
Conclusions:
- Tubular atrophy/interstitial fibrosis is the primary pathological feature associated with poor renal outcomes in Chinese children with IgAN.
- The Oxford classification's T score is crucial for risk stratification in pediatric IgAN.
- Further validation of the Oxford classification in diverse ethnic groups is warranted.
Background:
The Oxford classification of IgA nephropathy (IgAN) provides a useful tool for prediction of renal prognosis. However, the application of this classification in children with IgAN needs validation in different patient populations.
Methods:
A total of 218 children with IgAN from 7 renal centers in China were enrolled. The inclusion criteria was similar to the original Oxford study.
Results:
There were 98 patients (45%) with mesangial proliferation (M1), 51 patients (23%) with endocapillary proliferation (E1), 136 patients (62%) with segmental sclerosis/adhesion lesion (S1), 13 patients (6%) with moderate tubulointerstitial fibrosis (T1 26-50% of cortex scarred), and only 2 patients (1%) with severe tubulointerstitial fibrosis (T2, >50% of cortex scarred). During a median follow-up duration of 56 months, 24 children (12.4%) developed ESRD or 50% decline in renal function. In univariate COX analysis, we found that tubular atrophy/interstitial fibrosis (HR 4.3, 95%CI 1.8-10.5, P < 0.001) and segmental glomerulosclerosis (HR 9.2 1.2-68.6, P = 0.03) were significant predictors of renal outcome. However, mesangial hypercellularity, endocapillary proliferation, crescents, and necrosis were not associated with renal prognosis. In the multivariate COX regression model, none of these pathologic lesions were shown to be independent risk factors of unfavorable renal outcome except for tubular atrophy/interstitial fibrosis (HR 2.9, 95%CI 1.0-7.9 P = 0.04).
Conclusions:
We confirmed tubular atrophy/interstitial fibrosis was the only feature independently associated with renal outcomes in Chinese children with IgAN.
Related Concept Videos
Chronic Kidney Disease III: Interprofessional Care
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Acute Kidney Injury I: Introduction
Kidney Transplant I: Introduction
Nephrotic Syndrome I : Introduction
Chronic Kidney Disease I: Introduction
