Evidence map›Paper›PMID 42006224›Full record

ArticleKidney international reports2026

Outcomes in Children and Adults With Antiglomerular Basement Membrane Disease.

Adriana Suhlrie, Wilbert A G van der Meijden, Stanislas Faguer, Federico Alberici, Anisa Idrizi, Vincent Audard, Aude Servais, Olivia Boyer, Claire Dossier, Jörg Radermacher and 13 more

Abstract read
In one paragraph

Article in Kidney international reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

23 authors.

Adriana SuhlrieDepartment of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.
Wilbert A G van der MeijdenDepartment of Nephrology, Radboud University Medical Center, Nijmegen, The Netherlands.
Stanislas FaguerDepartment of Nephrology and Organ Transplantation, Centre Hospitalier Universitaire de Toulouse, National Reference Centre for Rare Kidney Diseases, Toulouse, France.
Federico AlbericiNephrology Unit, University of Brescia, ASST Spedali Civili, Brescia, Italy.
Anisa IdriziNephrology Unit, University of Brescia, ASST Spedali Civili, Brescia, Italy.
Vincent AudardNephrology and Renal Transplantation Department, Assistance Publique-Hôpitaux de Paris, Universite Paris Est Créteil, Institut National de la Santé et de la Recherche Médicale U955, Institut Mondor de Recherche Biomédicale, Henri Mondor University Hospital, Créteil, France.
Aude ServaisDepartment of Nephrology and Transplantation, Hôpital Necker Enfants Malades, APHP, Institut Imagine, Université Paris Cité, Paris, France.
Olivia BoyerNéphrologie pédiatrique, Hôpital Necker Enfants Malades, Institut Imagine, Université Paris Cité, Paris, France.
Claire DossierDepartment of Pediatric Nephrology, Robert-Debré Hospital, APHP, Paris, France.
Jörg RadermacherJohannes Wesling Klinikum Minden, Minden, Germany.
Chrysanthi SkaliotiClinic of Nephrology and Renal Transplantation, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Jakub ZiegDepartment of Pediatrics, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Marina AksenovaY. Veltischev Research and Clinical Institute for Pediatrics and Pediatric Surgery at the Pirogov Russian National Research Medical University, Moscow, Russia.
Ann RaesDepartment of Pediatric Nephrology and Rheumatology, Ghent University Hospital, Ghent University, ERKNET Centre, Ghent, Belgium.
Thomas RensonDepartment of Pediatric Nephrology and Rheumatology, Ghent University Hospital, Ghent University, ERKNET Centre, Ghent, Belgium.
Antonio MastrangeloFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Eiske DorresteijnDepartment of Pediatric Nephrology, Sophia Children's Hospital, Erasmus Medical Center, Rotterdam, Netherlands.
Alexandra TerziKlinik für Kinderheilkunde II, Universitätsklinikum Essen, Essen, Germany.
Antonia BoutsEmma Children's Hospital, Department of Pediatric Nephrology, Amsterdam UMC, Amsterdam, The Netherlands.
Ana Fernandes TeixeiraUnidade Local de Saúde de Santo António, Porto, Portugal.
Maria Herrero-GoñiDepartment of Pediatric Nephrology, IIS BioBizkaia Health Research Institute, Cruces University Hospital, University of Deusto, University of the Basque Country UPV/EHU, Barakaldo, Bizkaia, Spain.
Dieter HaffnerDepartment of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.
Nele KanzelmeyerDepartment of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Antiglomerular basement membrane (anti-GBM) disease is a rare, small-vessel vasculitis because of antibodies targeting the glomerular and alveolar capillaries, leading to rapidly progressive glomerulonephritis and/or pulmonary hemorrhage. Data on children with anti-GBM are scarce. Methods: We collected clinical and biochemical data from European pediatric and adult patients diagnosed with anti-GBM disease between 2020 and 2024. Results: A total of 72 patients (35% children) with anti-GBM disease and with a median follow-up of 18 months were analyzed. Pediatric cases were more often female and had higher estimated glomerular filtration rate (eGFR) at the time of diagnosis (each Conclusion: Our study indicates that girls predominate among children with anti-GBM disease and that children have a better outcome in terms of eGFR than adults, which is at least partly because of better eGFR values at diagnosis. The need for dialysis is a strong predictor of outcome, regardless of age.

Indexed as

antiglomerular basement membrane diseaseautoantibodieschildrenglomerulonephritisGoodpasture syndromeoutcome

Identifiers

PMID42006224
PMCPMC13090544

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.