The new histopathologic classification of ANCA-associated GN and its association with renal outcomes in childhood

Clin J Am Soc Nephrol. 2014 Oct 7;9(10):1684-91. doi: 10.2215/CJN.01210214. Epub 2014 Aug 21.

Abstract

Background and objectives: A proposed histopathologic classification for ANCA-associated GN is predictive of long-term renal outcome in adult populations. This study sought to validate this system in a pediatric cohort.

Design, setting, participants, & measurements: This was a retrospective, single-center, cohort study of 40 children diagnosed and followed until their transition to adult care at one institution between 1987 and 2012. Renal biopsy specimens were reviewed by a pathologist blinded to patient outcome and were classified using the new histopathologic classification system of focal, crescentic, mixed, and sclerotic groups. Time to the composite outcome of CKD stages 3 and 4 (determined by eGFR with repeated creatinine measures using the Schwartz equation) or ESRD (defined as dialysis dependence or transplantation) were ascertained.

Results: The study population consisted of 40 children (70% female), followed for a median of 2.4 years. The biopsy specimens were categorized as focal in 13 patients (32.5%), crescentic in 20 (50%), mixed in two (5%), and sclerotic in five (12.5%). Mixed and crescentic were combined for analyses. Survival analysis of time to the composite renal endpoint of at least 3 months of eGFR<60 ml/min per 1.73 m(2) or ESRD differed significantly among the three biopsy groups log-rank P<0.001), with an adjusted hazard ratio of 3.14 (95% confidence interval, 0.68 to 14.4) in the crescentic/mixed group and 23.6 (95% confidence interval, 3.9 to 144.2) in the sclerotic category compared with the focal category. The probability of having an eGFR>60 ml/min per 1.73 m(2) at 2 years was 100% for the focal, 56.5% for the crescentic/mixed, and 0% for the sclerotic biopsy categories.

Conclusions: This study showed the clinical utility of this histopathologic classification system and its ability to discriminate renal outcomes among children with ANCA GN.

Keywords: ANCA; glomerulonephritis; pediatric nephrology; renal biopsy; vasculitis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Adolescent
  • Age Factors
  • Antibodies, Antineutrophil Cytoplasmic / immunology*
  • Biopsy
  • Child
  • Disease Progression
  • Female
  • Glomerular Filtration Rate
  • Glomerulonephritis / classification
  • Glomerulonephritis / immunology*
  • Glomerulonephritis / mortality
  • Glomerulonephritis / pathology*
  • Glomerulonephritis / physiopathology
  • Glomerulonephritis / therapy
  • Glomerulosclerosis, Focal Segmental / immunology
  • Glomerulosclerosis, Focal Segmental / pathology
  • Humans
  • Kaplan-Meier Estimate
  • Kidney / immunology*
  • Kidney / pathology*
  • Kidney / physiopathology
  • Kidney Failure, Chronic / immunology
  • Kidney Failure, Chronic / pathology
  • Male
  • Ontario
  • Predictive Value of Tests
  • Prognosis
  • Proportional Hazards Models
  • Renal Insufficiency, Chronic / immunology*
  • Renal Insufficiency, Chronic / mortality
  • Renal Insufficiency, Chronic / pathology
  • Renal Insufficiency, Chronic / therapy
  • Reproducibility of Results
  • Retrospective Studies
  • Risk Factors
  • Time Factors

Substances

  • Antibodies, Antineutrophil Cytoplasmic