Abstract

There is no effectual pathological factor to predict the long-term renal prognosis of IgA nephropathy. Glomerular hypertrophy plays a crucial role in kidney disease outcomes in both experimental models and humans. This study aimed to 1) confirm the long-term prognostic significance of a maximal glomerular diameter (Max GD) ≥ 242.3 μm, 2) test a renal prognosis prediction model adding Max GD ≥ 242.3 μm to the Oxford classification (MEST-C), and 3) examine the time series changes in the long-term renal prognosis of patients with IgA nephropathy. The study included 43 patients diagnosed with IgA nephropathy from 1993 to 1998 at Kameda General Hospital. Renal prognosis with the endpoint of a 50% reduction in estimated glomerular filtration rate (eGFR) or the development of end-stage renal disease requiring dialysis was examined using logistic regression analysis, Cox regression analysis, and the Kaplan-Meier method. Pathological evaluation was performed using MEST-C and Max GD, and the validity of the prediction model was evaluated. Patients with Max GD ≥ 242.3 μm had significantly poor renal prognosis with multivariate Cox analysis (P = 0.0293). The results of the Kaplan-Meier analysis showed that kidney survival rates in the high-Max GD group were significantly lower than those in the low-Max GD group (log rank, P = 0.0043), which was confirmed in propensity score-matched models (log rank, P = 0.0426). Adding Max GD ≥ 242.3 μm to MEST-C improved diagnostic power of the renal prognosis prediction model by renal pathology tissue examination (R2: 3.3 to 14.5%, AICc: 71.8 to 68.0, C statistic: 0.657 to 0.772). We confirm that glomerular hypertrophy is useful as a long-term renal prognostic factor.

Highlights

  • Long-term renal prognoses of kidney diseases are clinically relevant, there is no established histopathological factor to predict the long-term renal prognosis of IgA nephropathy (IgAN)

  • We have previously reported that glomerular hypertrophy with a maximum glomerular diameter (Max maximal glomerular diameter (GD)) of 242.3 μm or more as an aggravating factor for renal prognosis of IgAN patients observed for 10 years [7]

  • Time series changes in pseudo-R2 values for long-term renal prognosis in IgAN patients following parameters: mesangial hypercellularity (M0: < 50% of glomeruli showing hypercellularity; M1: > 50% of glomeruli showing hypercellularity), endocapillary hypercellularity (E0: absent; E1: present), segmental glomerulosclerosis (S0: absent; S1: present), tubular atrophy/ interstitial fibrosis (T0: < 25%; T1: 25–50%; T2: > 50% of cortical area involved), and cellular/ fibrocellular crescents (C0: absent; C1: present in a least 1 but

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Summary

Introduction

Long-term renal prognoses of kidney diseases are clinically relevant, there is no established histopathological factor to predict the long-term renal prognosis of IgA nephropathy (IgAN). Coppo et al conducted long-term follow-up analyses of the original Validation Study of the Oxford Classification for IgA Nephropathy cohort, and showed an independent relationship between kidney biopsy findings and the risk of progression towards kidney failure in patients with IgAN. In their prognostic analyses, inclusion of the entire set of pathology lesions provided only a slight gain (+1.8%) in discriminatory power over that of the clinical variables alone for the entire follow-up duration [2]. The aim of the present study is to examine the prediction efficacy a model in which Max GD 242.3 μm was added to the Oxford classification (MEST-C) in IgAN cases with longterm data on kidney disease progression

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