Frontiers in Immunology (Mar 2022)

Assessment of Renal Risk Score and Histopathological Classification for Prediction of End-Stage Kidney Disease and Factors Associated With Change in eGFR After ANCA-Glomerulonephritis Diagnosis

  • Benoit Brilland,
  • Benoit Brilland,
  • Charlotte Boud’hors,
  • Charlotte Boud’hors,
  • Marie-Christine Copin,
  • Marie-Christine Copin,
  • Pierre Jourdain,
  • Nicolas Henry,
  • Samuel Wacrenier,
  • Samuel Wacrenier,
  • Assia Djema,
  • Clément Samoreau,
  • Jean-Philippe Coindre,
  • Maud Cousin,
  • Jeremie Riou,
  • Jeremie Riou,
  • Anne Croue,
  • Jean-Paul Saint-André,
  • Jean-François Subra,
  • Jean-François Subra,
  • Giorgina Barbara Piccoli,
  • Jean-François Augusto,
  • Jean-François Augusto

DOI
https://doi.org/10.3389/fimmu.2022.834878
Journal volume & issue
Vol. 13

Abstract

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IntroductionThe “Renal Risk Score” (RRS) and the histopathological classification have been proposed to predict the risk of end-stage kidney disease (ESKD) in ANCA-associated glomerulonephritis (ANCA-GN). Besides, factors associated with kidney function recovery after ANCA-GN onset remain to be more extensively studied. In the present study, we analyzed the value of the RRS and of the histopathological classification for ESKD prediction. Next, we analyzed factors associated with eGFR change within the first 2 years following ANCA-GN diagnosis.Materials and MethodsWe included patients from the Maine–Anjou ANCA-associated vasculitis registry with at least 6 months of follow-up. The values of ANCA-GN, histopathological classification, and RRS, and the factors associated with eGFR variations between ANCA-GN diagnosis and 2 years of follow-up were assessed.ResultsThe predictive values of the histopathological classification and RRS were analyzed in 123 patients. After a median follow-up of 42 months, 33.3% patients developed ESKD. The predictive value of RRS for ESKD was greater than that of the histopathological classification. Determinants of eGFR variation were assessed in 80/123 patients with complete eGFR measurement. The median eGFR increased from ANCA-GN diagnosis to month 6 and stabilized thereafter. The only factor associated with eGFR variation in our study was eGFR at ANCA-GN diagnosis, with higher eGFR at diagnosis being associated with eGFR loss (p<0.001).ConclusionThe RRS has a better predictive value for ESKD than the histopathological classification. The main determinant of eGFR variation at 2 years was eGFR at ANCA-GN diagnosis. Thus, this study suggests that eGFR recovery is poorly predicted by histological damage at ANCA-GN diagnosis.

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