Evidence map›Paper›PMID 37174733›Full record

ArticleCells2023

Ratio of Urinary Proteins to Albumin Excretion Shifts Substantially during Progression of the Podocytopathy Alport Syndrome, and Spot Urine Is a Reliable Method to Detect These Pathologic Changes.

Jan Boeckhaus, Lea Mohr, Hassan Dihazi, Burkhard Tönshoff, Lutz T Weber, Lars Pape, Kay Latta, Henry Fehrenbach, Baerbel Lange-Sperandio, Matthias Kettwig and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01485978 (Early Prospective Therapy Trial to Delay Renal Failure in Children With Alport Syndrome), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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.

NCT01485978 phase3completednot on this map

Early Prospective Therapy Trial to Delay Renal Failure in Children With Alport Syndrome

TypeinterventionalSponsorInstitut fuer anwendungsorientierte Forschung und klinische Studien GmbHRan2012 to 2019Enrolled66ConditionsRenal Insufficiency, ChronicArmsRamipril, placebo to ramipril
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Diagnosis, management and treatment of the Alport syndrome - 2024 guideline on behalf of ERKNet, ERA and ESPN.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Guideline
  2. Article
  3. Article
  4. Article
  5. Article
  6. Protocol and rationale for a randomized controlled SGLT2 inhibitor trial in paediatric and young adult populations with chronic kidney disease: DOUBLE PRO-TECT Alport.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Article
  7. SGLT2-Inhibition in Patients With Alport Syndrome.Kidney international reports · 2024
    Article
  8. [Macrohematuria in children and adolescents].Urologie (Heidelberg, Germany) · 2024
    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

19 authors at 13 institutions in 1 country.

Jan BoeckhausClinic for Nephrology and Rheumatology, University Medical Center Goettingen, 37075 Goettingen, Germany.
Lea MohrClinic for Nephrology and Rheumatology, University Medical Center Goettingen, 37075 Goettingen, Germany.
Hassan DihaziClinic for Nephrology and Rheumatology, University Medical Center Goettingen, 37075 Goettingen, Germany.ORCID 0000-0003-3417-0385
Burkhard TönshoffDepartment of Pediatrics I, University Children's Hospital Heidelberg, 69120 Heidelberg, Germany.
Lutz T WeberPediatric Nephrology, Children's and Adolescents' Hospital, Faculty of Medicine and University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.
Lars PapeDepartment of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, 30625 Hannover, Germany.
Kay LattaClementine Kinderhospital Frankfurt, 60316 Frankfurt, Germany.
Henry FehrenbachPediatric Nephrology, Children's Hospital, 87700 Memmingen, Germany.
Baerbel Lange-SperandioDr. v. Hauner Children's Hospital, Ludwig Maximilians University, 80337 Munich, Germany.ORCID 0000-0001-8898-3459
Matthias KettwigClinic of Pediatrics and Adolescent Medicine, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0003-4804-7716
Hagen StaudePediatric Nephrology, University Children's Hospital Rostock, 18057 Rostock, Germany.
Sabine KönigUniversity Children's Hospital Münster, 48149 Münster, Germany.
Ulrike John-KroegelDivision of Pediatric Nephrology, University Children's Hospital, 07743 Jena, Germany.
Jutta GellermannPediatric Nephrology, Charité Children's Hospital, 10117 Berlin, Germany.
Bernd HoppeDivision of Pediatric Nephrology, Department of Pediatrics, University of Bonn, 53121 Bonn, Germany.
Matthias GalianoDepartment of Pediatrics and Adolescent Medicine, University Hospital, Friedrich-Alexander-University Erlangen, 91054 Erlangen, Germany.
Dieter HaffnerDepartment of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-9601-7813
Heidrun RhodeDepartment of Internal Medicine I, Cardiology, Angiology, Intensive Medical Care, University Hospital Jena, Am Klinikum 1, 07747 Jena, Germany.
Oliver GrossClinic for Nephrology and Rheumatology, University Medical Center Goettingen, 37075 Goettingen, Germany.ORCID 0000-0002-8390-8852
Jena University Hospital · DEMedizinische Hochschule Hannover · DEBürgerhospital Frankfurt am Main · DECharité - Universitätsmedizin Berlin · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHeidelberg University · DEKernkraftwerk Gundremmingen · DELudwig-Maximilians-Universität München · DEUniversitätsmedizin Göttingen · DEUniversity Hospital Münster · DEUniversity of Bonn · DEUniversity of Cologne · DEUniversity of Rostock · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The urinary albumin- and protein-to-creatinine ratios (UACR and UPCR, respectively) are key endpoints in most clinical trials assessing risk of progression of chronic kidney disease (CKD). For the first time, the current study compares the UACR versus the UPCR head-to-head at early stages of CKD, taking use of the hereditary podocytopathy Alport syndrome (AS) as a model disease for any CKD. Urine samples originated from the prospective randomized, controlled EARLY PRO-TECT Alport trial (NCT01485978). Urine samples from 47 children with confirmed diagnoses of AS at very early stages of CKD were divided according to the current stage of AS: stage 0 (UACR < 30 mg/g), stage 1 (30-300 mg/g) or stage 2 (>300 mg/g). The range of estimated glomerular filtration rate was 75-187.6 mL/min. The mean age was 10.4 ± 4.5 years. In children at stage 0, proteinuria in spot urine, confirmed in 24 h urine, was almost ten times higher than albuminuria (106.4 ± 42.2 vs. 12.5 ± 9.7;

Indexed as

Nephritis, HereditaryRenal Insufficiency, ChronicAdolescentAlbuminsAlbuminuriaChildCreatinineHumansProspective StudiesAlbuminsCreatininealbuminuriaAlport syndromediagnostic markerglomerulushereditary kidney diseasesmechanical stretchpodocytespodocytopathiesproteinuriarenal fibrosistype IV collagen

Identifiers

PMID37174733
PMCPMC10177071
OpenAlexW4375866691

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.