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Updated: Sep 15, 2025

Mouse Kidney Transplantation: Models of Allograft Rejection
Published on: October 11, 2014
Validation of 2 Prognostic Models to Predict Renal Allograft Outcome After IgA Nephropathy Recurrence
Emilio Rodrigo1, Luis F Quintana2, Teresa Vázquez-Sánchez3
1Nephrology Department, Hospital Universitario Marqués de Valdecilla/IDIVAL, Universidad de Cantabria, Santander, Spain.
Introduction:
IgA nephropathy (IgAN) recurrence (IgANr) after kidney transplantation (KTx) is common and contributes to reducing graft survival. Some tools have been developed to predict the patients who are at a higher risk of poor outcomes among the native (international IgAN prediction tool [IIgAN-PT]) and graft (Bednarova's prediction tool [Bednarova-PT]) kidney. We aimed to analyze their performance in a KTx population other than the originally reported.
Methods:
We performed a multicenter retrospective study including KTx with biopsy-proven IgANr. IIgAN-PT and Bednarova-PT were used to calculate the risk of death-censored graft loss (DCGL). We assessed the performance of both prediction models using discrimination and calibration metrics and Kaplan-Meier plots.
Results:
One hundred twenty KTx with IgANr were included. The time-dependent receiver operating characteristic (ROC) area under the curve (AUC) of Bednarova-PT for predicting DCGL was 83.5 (95% CI: 72.3-94.7) and the calibration slope was 0.96 (95% CI: 0.37-1.49). The time-dependent ROC AUC of IIgAN-PT for predicting DCGL was 87.3 (95% CI: 77.58-97.02) and the calibration slope was 2.49 (95% CI: 0.19-4.13). IIgAN-PT tended to underestimate the graft-loss risk in high-risk individuals. The Kaplan-Meier curve of the highest risk group, defined by using both prediction tools, was clearly separated from the other curves.
Conclusion:
Both IIgAN-PT and Bednarova-PT performed well in predicting DCGL after IgANr and should be used to identify those KTx at the highest risk. Both models had good discriminatory ability and were well-calibrated, although the calibration slope was higher for IIgAN-PT, tending to underestimate the risk in high-risk individuals.
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