Evidence map›Paper›PMID 36227435›Full record

ArticlePediatric nephrology (Berlin, Germany)2023

Epidemiology and clinicopathological characteristics of native kidney disease in children in Flanders, Belgium.

Dries Deleersnijder, Noël Knops, Dominique Trouet, Koen Van Hoeck, Sevasti Karamaria, Johan Vande Walle, Reiner Mauel, Louise Cools, Gert Meeus, Amélie Dendooven and 4 more

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In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

14 authors at 7 institutions in 1 country.

Dries DeleersnijderLaboratory of Molecular Immunology, Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Louvain, Belgium. dries.deleersnijder@kuleuven.be.ORCID 0000-0002-8285-6624
Noël KnopsPediatric Nephrology and Solid Organ Transplantation, University Hospitals Leuven, Louvain, Belgium.
Dominique TrouetLaboratory of Experimental Medicine and Pediatrics, University of Antwerp, Antwerp, Wilrijk, Belgium.
Koen Van HoeckDepartment of Pediatric Nephrology, Antwerp University Hospital, Edegem, Belgium.
Sevasti KaramariaDepartment of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.
Johan Vande WalleDepartment of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.
Reiner MauelDepartment of Pediatrics, University Hospital Brussels, Brussels, Belgium.
Louise CoolsLaboratory of Molecular Immunology, Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Louvain, Belgium.
Gert MeeusDepartment of Nephrology, AZ Groeninge Hospital, Kortrijk, Belgium.
Amélie DendoovenLaboratory of Experimental Medicine and Pediatrics, University of Antwerp, Antwerp, Wilrijk, Belgium.
Johan De MeesterDepartment of Nephrology and Dialysis, VITAZ Hospital, Sint-Niklaas, Belgium.
Wim LaurensDepartment of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.
Ben SprangersLaboratory of Molecular Immunology, Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Louvain, Belgium. ben.sprangers@zol.be.
FCGG collaborative group
Ghent University Hospital · BERega Institute for Medical Research · BEUniversity of Antwerp · BEAntwerp University Hospital · BEAZ Groeninge · BEKU Leuven · BEVlaamse Vereniging voor Obstetrie en Gynaecolo · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Flemish Collaborative Glomerulonephritis Group (FCGG) registry is a population-based kidney biopsy registry that has been including all native kidney biopsies performed in children in Flanders (Belgium), since 2017.

methodsFrom 2017 to 2020, 148 pediatric (< 18 years) native kidney biopsies were included. Each biopsy received a histopathological and final nephrological diagnosis, and concordance between both was assessed. Disease chronicity, summarized by the Mayo Clinic Chronicity Score, was determined on 122 biopsies with > 5 glomeruli.

resultsKidney biopsy rate was high (29.0 biopsies per million children per year), median age was 10.0 years (IQR 5.8-14.7), and boys predominated (56.1% males). A total of 140 biopsies (94.6%) showed a representative pathology result. Glomerular disease was most prevalent, with IgA nephropathy/IgA vasculitis (43 biopsies, 29.1%) and minimal change disease (MCD) (29 biopsies, 19.6%) being the overall most frequent diagnoses. In general, diagnostic concordance was high (80.7%). In Alport syndrome and focal segmental glomerulosclerosis (FSGS), concordance was lower, as the nephrological diagnosis was often determined by results of genetic analysis. Nephrotic syndrome was the most frequent indication for kidney biopsy (31.8%) and was mainly caused by MCD and FSGS. The degree of disease chronicity on kidney biopsies was generally low, although 27.3% of biopsies with a diagnosis of FSGS showed moderate-to-severe chronic damage.

conclusionsThe presented epidemiological findings validate data from previous European registry studies and may inspire kidney biopsy registries worldwide to implement novel features such as clinicopathological concordance and chronicity grading. A higher resolution version of the Graphical abstract is available as Supplementary information.

Indexed as

GlomerulonephritisGlomerulonephritis, IGAGlomerulosclerosis, Focal SegmentalNephrosis, LipoidBelgiumBiopsyChildFemaleHumansKidneyMaleEpidemiologyKidney biopsyMCCSNative kidneyRegistry

Identifiers

PMID36227435
OpenAlexW4304891741

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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.