Evidence map›Paper›PMID 23903693›Full record

ArticlePediatric nephrology (Berlin, Germany)2013

Phospholipase A2 receptor staining in pediatric idiopathic membranous glomerulopathy.

L Nicholas Cossey, Patrick D Walker, Chris P Larsen

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Article in Pediatric nephrology (Berlin, Germany), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

20 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
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  10. Article
  11. Proteinuria in a patient with Graves' disease: Answers.Pediatric nephrology (Berlin, Germany) · 2019
    Article
  12. Proteinuria in a patient with Graves' disease: Questions.Pediatric nephrology (Berlin, Germany) · 2019
    Article
  13. Genetics of membranous nephropathy.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2018
    Review
  14. Article
  15. M-type phospholipase APediatric nephrology (Berlin, Germany) · 2017
    Article
  16. Review
  17. Article
  18. Article
  19. Membranous nephropathy: not just a disease for adults.Pediatric nephrology (Berlin, Germany) · 2015
    Review
  20. Article
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

3 authors at 2 institutions in 1 country.

L Nicholas CosseyNephropath, 10810 Executive Center Dr. Suite 100, Little Rock, AR, 72211, USA, nich.cossey@nephropath.com.
Patrick D Walker
Chris P Larsen
Arkana Laboratories · USUniversity of Arkansas for Medical Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMembranous glomerulopathy, though typically a disease of adults, does occur in children. Antiphospholipase A2 receptor (PLA2R) autoantibodies have recently been implicated as a causative agent in most cases of adult primary (idiopathic) membranous glomerulopathy. PLA2R staining of renal biopsies in two recent large case series of adults with primary membranous glomerulopathy showed a sensitivity of approximately 75 % for detecting primary membranous glomerulopathy. To our knowledge, this is the largest study of its kind to assess PLA2R staining in a pediatric population.

methodsForty-one consecutive cases of pediatric membranous glomerulopathy were identified from our database, and clinical follow-up was performed to confirm primary membranous glomerulopathy. Twenty-two patients met inclusion criteria and are the subject of this report.

resultsGranular, capillary loop immunofluorescence staining for immunoglobulin G (IgG) was present in 100 % of patients, and C3 staining was present in 77 %. PLA2R staining was identified in ten patients, providing a sensitivity of 45 % [confidence interval (CI) 25-67 %]. Bovine serum albumin staining was performed in all PLA2R-negative cases and showed no positivity. Morphologic findings associated with negative PLA2R staining included segmental membranous lesions, mesangial and subendothelial deposits, C1q and "full-house" staining, and lower-stage lesions by electron microscopy. At 38 months' average follow-up, all patients were still considered as having primary membranous glomerulopathy, with none developing a clinically detectable secondary etiology.

conclusionsPLA2R staining sensitivity is much lower in the pediatric than the adult primary membranous glomerulopathy population. This finding suggests a more diverse and currently incompletely described set of etiologies for this disease in this group.

Indexed as

AdolescentAge FactorsBiomarkersBiopsyChildChild, PreschoolComplement C1qComplement C3FemaleFluorescent Antibody TechniqueGlomerulonephritis, MembranousHumansImmunoglobulin GKidneyMalePredictive Value of TestsBiomarkersComplement C1qComplement C3Immunoglobulin GPLA2R1 protein, humanReceptors, Phospholipase A2

Identifiers

PMID23903693
OpenAlexW1985808460

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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.