Evidence map›Paper›PMID 38765578›Full record

ArticleKidney international reports2024

Steroid-Resistant Nephrotic Syndrome due to

Jessica Kachmar, Olivia Boyer, Beata Lipska-Ziętkiewicz, Vincent Morinière, Olivier Gribouval, Laurence Heidet, Irena Balasz-Chmielewska, Elisa Benetti, Sylvie Cloarec, Dagmar Csaicsich and 16 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Kidney international reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Evaluation for genetic disease in kidney transplant candidates: A practice resource.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Review
  3. Article
  4. 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

26 authors.

Jessica KachmarLaboratoire des Maladies Rénales Héréditaires, Inserm UMR 1163, Imagine Institute for Genetic Diseases, Université Paris Cité, Paris, France.
Olivia BoyerLaboratoire des Maladies Rénales Héréditaires, Inserm UMR 1163, Imagine Institute for Genetic Diseases, Université Paris Cité, Paris, France.
Beata Lipska-ZiętkiewiczCentre for Rare Diseases and Clinical Genetics Unit, Medical University of Gdansk, Gdansk, Poland.
Vincent MorinièreService de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance publique, Hôpitaux de Paris (AP-HP), Paris, France.
Olivier GribouvalLaboratoire des Maladies Rénales Héréditaires, Inserm UMR 1163, Imagine Institute for Genetic Diseases, Université Paris Cité, Paris, France.
Laurence HeidetLaboratoire des Maladies Rénales Héréditaires, Inserm UMR 1163, Imagine Institute for Genetic Diseases, Université Paris Cité, Paris, France.
Irena Balasz-ChmielewskaDepartment of Pediatrics, Nephrology and Hypertension, Medical University of Gdansk, Gdansk, Poland.
Elisa BenettiPediatric Nephrology Unit, Padua University Hospital, Padua, Italy.
Sylvie CloarecService de Néphrologie-Hémodialyse pédiatrique, Centre de compétence Maladies Rénales Rares, CHRU Tours-Clocheville, Tours, France.
Dagmar CsaicsichDepartment of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
Stéphane DecramerPediatric Nephrology Unit, Toulouse University Hospital; Centre De Référence Des Maladies Rénales Rares du Sud-Ouest, SoRare; INSERM U1048, Institute of Cardiovascular and Metabolic Diseases, Toulouse, France.
Jutta GellermannKlinik für Pädiatrie/Nephrologie, Charité Campus Virchox-Klinikum, Berlin, Germany.
Vincent GuigonisPediatrics, Hôpital de la mère et de l'enfant, Limoges, France.
Julien HoganPediatric Nephrology, Hôpital Universitaire Robert-Debré; Paris Translational Research Center for Organ Transplantation, Inserm UMR-S970, Université Paris Cité, Paris, France.
Aysun Karabay BayazitDivision of Pediatric Nephrology, Cukurova University, Adana, Türkiye.
Anette MelkChildren's Hospital, Hannover Medical School, Hannover, Germany.
Nazym NigmatullinaNational Research Center for Maternal and Child Heatlh, Astana, Kazakhstan.
Jun OhPediatric Nephrology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Fatih OzaltinDepartment of Pediatric Nephrology, Hacettepe University, Faculty of Medicine, Sihhiye, Ankara, Türkiye.
Bruno RanchinPediatric Nephrology Unit, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Université de Lyon, Lyon, France.
Michel TsimaratosFaculté de médecine de Marseille, Université de la Méditerranée, Marseille, France.
Agnes TrautmannDepartment of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University of Heidelberg, Germany.
Corinne AntignacLaboratoire des Maladies Rénales Héréditaires, Inserm UMR 1163, Imagine Institute for Genetic Diseases, Université Paris Cité, Paris, France.
Franz SchaeferDepartment of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University of Heidelberg, Germany.
Guillaume DorvalLaboratoire des Maladies Rénales Héréditaires, Inserm UMR 1163, Imagine Institute for Genetic Diseases, Université Paris Cité, Paris, France.
PodoNet Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Unlike idiopathic nephrotic syndrome (NS), hereditary podocytopathies are not expected to recur after kidney transplantation. However, some reports of posttransplant recurrence of NS in patients carrying variants in the Methods: Since January 2010, 61 patients identified at Necker-Enfants Malades Hospital and 56 enrolled in the PodoNet Registry with biallelic variants in the Results: Of the 117 patients, 23 carried the p.Arg138Gln variant in the homozygous state and 16 in the compound heterozygous state. The other 78 patients carried different variants in the homozygous ( Conclusion: In this large cohort, the risk of patients with causative variants in the

Indexed as

glomerular diseasehereditary nephrotic syndromekidney transplantationNPHS2 geneposttransplant recurrencesteroid-resistant nephrotic syndrome

Identifiers

PMID38765578
PMCPMC11101709

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.