Evidence map›Paper›PMID 36090483›Full record

ArticleKidney international reports2022

Refining Kidney Survival in 383 Genetically Characterized Patients With Nephronophthisis.

Jens Christian König, Rebeka Karsay, Joachim Gerß, Karl-Peter Schlingmann, Mareike Dahmer-Heath, Anna-Katharina Telgmann, Sabine Kollmann, Gema Ariceta, Valentine Gillion, Detlef Bockenhauer and 22 more

Abstract read
In one paragraph

Article in Kidney international reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  4. Genetic kidney disease in adults-the pathologists' perspective.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2026
    Review
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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

32 authors.

Jens Christian KönigDepartment of General Pediatrics, University Children's Hospital Münster, Münster, Germany.
Rebeka KarsayDepartment of General Pediatrics, University Children's Hospital Münster, Münster, Germany.
Joachim GerßInstitute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
Karl-Peter SchlingmannDepartment of General Pediatrics, University Children's Hospital Münster, Münster, Germany.
Mareike Dahmer-HeathDepartment of General Pediatrics, University Children's Hospital Münster, Münster, Germany.
Anna-Katharina TelgmannDepartment of General Pediatrics, University Children's Hospital Münster, Münster, Germany.
Sabine KollmannDepartment of General Pediatrics, University Children's Hospital Münster, Münster, Germany.
Gema AricetaServicio de Nefrología Pediátrica, Hospital Vall D'Hebron, Universitat Autónoma de Barcelona, Barcelona, Spain.
Valentine GillionDivision of Nephrology, Saint-Luc Academic Hospital, Université Catholique Louvain, Brussels, Belgium.
Detlef BockenhauerDepartment of Renal Medicine, University College London, London, UK.
Aurélia Bertholet-ThomasCentre de Référence des Maladies Rénales Rares-Néphrogones-Hôpital Femme Mère Enfant, Hospices Civils de Lyon-Filière ORKiD, Bron, France.
Antonio MastrangeloFondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Olivia BoyerService de Néphrologie Pédiatrique, Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Institut Imagine, Hôpital Necker-Enfants Malades, Université de Paris, Paris, France.
Marc LilienDepartment of Pediatric Nephrology, Wilhelmina Children's Hospital, University Medical Center Utrecht and Utrecht University, Utrecht, the Netherlands.
Stéphane DecramerInstitut National de la Santé et de la Recherche Médicale (INSERM), U1297, Institut of Cardiovascular and Metabolic Disease, Toulouse, France, Université Toulouse III Paul-Sabatier, Toulouse, France, Service de Néphrologie Pédiatrique, Hôpital des Enfants, CHU Toulouse, Toulouse, France, Centre De Référence des Maladies Rénales Rares du Sud-Ouest (SORARE), Toulouse, France.
Joost P SchanstraInstitut National de la Santé et de la Recherche Médicale (INSERM), U1297, Institut of Cardiovascular and Metabolic Disease, Toulouse, France, Université Toulouse III Paul-Sabatier, Toulouse, France, Service de Néphrologie Pédiatrique, Hôpital des Enfants, CHU Toulouse, Toulouse, France, Centre De Référence des Maladies Rénales Rares du Sud-Ouest (SORARE), Toulouse, France.
Martin PohlDepartment of Pediatrics, University Hospital Freiburg, Freiburg, Germany.
Raphael SchildUniversity Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Stefanie WeberUniversity Children's Hospital, Marburg, Germany.
Julia HoefeleInstitute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.
Jens DrubeDepartement of Pediatric Nephrology, Medical School Hannover, Hannover, Germany.
Metin CetinerDepartment of Pediatric Nephrology, Pediatrics II, University of Duisburg-Essen, Essen, Germany.
Matthias HansenClementine Kinderhospital, Frankfurt am Main, Germany.
Julia ThumfartDepartment of Pediatric Gastroenterology, Nephrology and Metabolic Diseases, Charité Universitätsmedizin Berlin, Berlin, Germany.
Burkhard TönshoffDepartment of Pediatrics I, University Children's Hospital Heidelberg, Heidelberg, Germany.
Sandra HabbigDepartment of Pediatrics, Center for Family Health and Center for Rare Diseases, Faculty of Medicine, University Hospital Cologne and University of Cologne, Cologne, Germany.
Max Christoph LiebauDepartment of Pediatrics, Center for Family Health and Center for Rare Diseases, Faculty of Medicine, University Hospital Cologne and University of Cologne, Cologne, Germany.
Martin BaldChildren's Hospital, Olgahospital, Klinikum Stuttgart, Stuttgart, Germany.
Carsten BergmannDepartment of Internal Medicine IV (Nephrology), Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Petra PennekampDepartment of General Pediatrics, University Children's Hospital Münster, Münster, Germany.
Martin KonradDepartment of General Pediatrics, University Children's Hospital Münster, Münster, Germany.
NEOCYST consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Nephronophthisis (NPH) comprises a group of rare disorders accounting for up to 10% of end-stage kidney disease (ESKD) in children. Prediction of kidney prognosis poses a major challenge. We assessed differences in kidney survival, impact of variant type, and the association of clinical characteristics with declining kidney function. Methods: Data was obtained from 3 independent sources, namely the network for early onset cystic kidney diseases clinical registry ( Results: A total of 383 individuals were available for analysis: 116 Conclusion: The presented data will enable clinicians to better estimate kidney prognosis of distinct patients with NPH and thereby allow personalized counseling.

Indexed as

end-stage kidney diseasegenetic variant severitygenotype-phenotype correlationskidney survivalnephronophthisisprognostic factors

Identifiers

PMID36090483
PMCPMC9459005

What OpenQuestion holds

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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.