Evidence map›Paper›PMID 25147157›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2014

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

Damien G Noone, Marinka Twilt, Wesley N Hayes, Paul S Thorner, Susanne Benseler, Ronald M Laxer, Rulan S Parekh, Diane Hebert

Abstract readValidation Study
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed.

  1. Article
  2. Article
  3. New avenues in childhood vasculitis.Pediatric rheumatology online journal · 2025
    Review
  4. Article
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  6. Article
  7. Article
  8. Article
  9. Article
  10. Rapidly progressive glomerulonephritis in children.Pakistan journal of medical sciences · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Damien G NooneDivisions of Nephrology.
Marinka TwiltRheumatology, and.
Wesley N HayesDivisions of Nephrology.
Paul S ThornerPathology, The Research Institute, and Department of Pathobiology and Laboratory Medicine and.
Susanne BenselerRheumatology, and The Research Institute, and Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Ronald M LaxerRheumatology, and Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Rulan S ParekhDivisions of Nephrology, The Research Institute, and Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada, and rulan.parekh@sickkids.ca.
Diane HebertDivisions of Nephrology, Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesA 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.

resultsThe 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.

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

Indexed as

AdolescentAge FactorsAntibodies, Antineutrophil CytoplasmicBiopsyChildDisease ProgressionFemaleGlomerular Filtration RateGlomerulonephritisGlomerulosclerosis, Focal SegmentalHumansKaplan-Meier EstimateKidneyKidney Failure, ChronicMaleOntarioAntibodies, Antineutrophil CytoplasmicANCAglomerulonephritispediatric nephrologyrenal biopsyvasculitis

Identifiers

PMID25147157
PMCPMC4186506

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.