Evidence map›Paper›PMID 28983704›Full record

ArticlePediatric nephrology (Berlin, Germany)2018

Presentation of pediatric Henoch-Schönlein purpura nephritis changes with age and renal histology depends on biopsy timing.

Imke Hennies, Charlotte Gimpel, Jutta Gellermann, Kristina Möller, Brigitte Mayer, Katalin Dittrich, Anja K Büscher, Matthias Hansen, Wiebke Aulbert, Elke Wühl and 21 more

Abstract read
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In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

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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

17 citing papers in PubMed.

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  11. The Efficacy ofEvidence-based complementary and alternative medicine : eCAM · 2021
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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

31 authors.

Imke HenniesDepartment of Pediatric Kidney, Liver and Metabolic Diseases, Children's Hospital, Hannover Medical School, Hannover, Germany.
Charlotte GimpelDepartment of General Pediatrics, Adolescent Medicine and Neonatology, Medical Center, University of Freiburg Faculty of Medicine, University of Freiburg, Mathildenstrasse 1, 79106, Freiburg, Germany.
Jutta GellermannDepartment of Pediatric Nephrology, Charité University Hospital, Berlin, Germany.
Kristina MöllerDepartment of Pediatrics, Klinikum Links der Weser, Bremen, Germany.
Brigitte MayerChildren's Hospital Dresden, Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Katalin DittrichChildren's Hospital, University of Leipzig, Leipzig, Germany.
Anja K BüscherDepartment of Pediatrics II, Children's Hospital, University of Duisburg-Essen, Essen, Germany.
Matthias HansenKfH Center of Pediatric Nephrology, Clementine Children's Hospital, Frankfurt, Germany.
Wiebke AulbertDepartment of Pediatrics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Elke WühlDivision of Pediatric Nephrology, Center for Pediatrics and Adolescent Medicine, University of Heidelberg, Heidelberg, Germany.
Richard NisselChildren's Hospital, Städtisches Klinikum, Karlsruhe, Germany.
Gessa SchalkPediatric Nephrology Unit, University Children's Hospital, Zurich, Switzerland.
Lutz T WeberDepartment of Pediatrics, University Hospital of Cologne, Cologne, Germany.
Michael PohlUniversity Children's Hospital, Jena, Germany.
Simone WygodaKfH Center of Pediatric Nephrology, St Georg Hospital, Leipzig, Germany.
Rolf BeetzDepartment of Pediatrics, Division of Pediatric Nephrology, Mainz University Medical Center, Mainz, Germany.
Günter KlausKfH Center of Pediatric Nephrology, University Hospital Marburg, Marburg, Germany.
Henry FehrenbachKfH Center of Pediatric Nephrology, Children's Hospital Memmingen, Memmingen, Germany.
Sabine KönigUniversity Children's Hospital Münster, Münster, Germany.
Hagen StaudeUniversity Children's Hospital, Rostock, Germany.
Ortraud BeringerUniversity Children's Hospital, Ulm, Germany.
Martin BaldChildren's Hospital, Olgahospital, Klinikum Stuttgart, Stuttgart, Germany.
Ulrike WaldenDepartment of Pediatrics II, Children's Hospital Augsburg, Augsburg, Germany.
Christian von SchnakenburgChildren's Hospital, Klinikum Esslingen, Esslingen am Neckar, Germany.
Gunhard BertramKrankenhaus St Elisabeth und St Barbara, Klinik für Kinder- und Jugendmedizin, Halle (Saale), Germany.
Michael WallotDepartment of Pediatrics, Bethanien Hospital, Moers, Germany.
Karsten HäffnerDepartment of General Pediatrics, Adolescent Medicine and Neonatology, Medical Center, University of Freiburg Faculty of Medicine, University of Freiburg, Mathildenstrasse 1, 79106, Freiburg, Germany.
Thorsten WiechNephropathology Section, Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Peter F HoyerDepartment of Pediatrics II, Children's Hospital, University of Duisburg-Essen, Essen, Germany.
Martin PohlDepartment of General Pediatrics, Adolescent Medicine and Neonatology, Medical Center, University of Freiburg Faculty of Medicine, University of Freiburg, Mathildenstrasse 1, 79106, Freiburg, Germany. martin.pohl@uniklinik-freiburg.de.
German Society of Pediatric Nephrology

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study correlates the clinical presentation of Henoch-Schönlein purpura nephritis (HSPN) with findings on initial renal biopsy.

methodsData from 202 pediatric patients enrolled in the HSPN registry of the German Society of Pediatric Nephrology reported by 26 centers between 2008 and 2014 were analyzed. All biopsy reports were re-evaluated for the presence of cellular crescents or chronic pathological lesions (fibrous crescents, glomerular sclerosis, tubular atrophy >5%, and interstitial fibrosis >5%).

resultsPatients with HSPN with cellular glomerular crescents were biopsied earlier after onset of nephritis (median 24 vs 36 days, p = 0.04) than those without, whereas patients with chronic lesions were biopsied later (57 vs 19 days, p < 0.001) and were older (10.3 vs 8.6 years, p = 0.01) than those without. Patients biopsied more than 30 days after the onset of HSPN had significantly more chronic lesions (52 vs 22%, p < 0.001), lower eGFR (88 vs 102 ml/min/1.73m

conclusionsIn summary, we find an age-dependent presentation of HSPN with a more insidious onset of non-nephrotic proteinuria, impaired renal function, longer delay to biopsy, and more chronic histopathological lesions in children above the age of 10 years. Thus, HSPN presents more like Immunoglobulin A (IgA) nephritis in older than in younger children.

Indexed as

Age FactorsBiopsyChildFemaleHumansIgA VasculitisKidneyMaleNephritisChildrenGlomerulosclerosisHenoch–Schönlein purpuraHistopathologyIgA NephritisKidney biopsy

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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.