Evidence map›Paper›PMID 36939917›Full record

ArticlePediatric nephrology (Berlin, Germany)2023

Low agreement between various eGFR formulae in pediatric and young adult ADPKD patients.

Pieter Schellekens, Marcelien Verjans, Peter Janssens, Angélique Dachy, Stéphanie De Rechter, Luc Breysem, Karel Allegaert, Bert Bammens, Rudi Vennekens, Pieter Vermeersch and 2 more

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Article in Pediatric nephrology (Berlin, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.1field-weighted citation impact, top 8% 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.

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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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

12 authors at 5 institutions in 2 countries.

Pieter SchellekensPKD Research Group, Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium.
Marcelien VerjansDepartment of Pediatric Nephrology, University Hospitals Leuven, Louvain, Belgium.
Peter JanssensPKD Research Group, Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium.
Angélique DachyPKD Research Group, Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium.
Stéphanie De RechterPKD Research Group, Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium.
Luc BreysemDepartment of Radiology, University Hospitals Leuven, Louvain, Belgium.
Karel AllegaertClinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, 3000, Louvain, Belgium.
Bert BammensDepartment of Microbiology, Immunology and Transplantation, Nephrology and Renal Transplantation Research Group, KU Leuven, Louvain, Belgium.
Rudi VennekensDepartment of Cellular and Molecular Medicine, VIB Centre for Brain and Disease Research, Laboratory of Ion Channel Research, KU Leuven, Louvain, Belgium.
Pieter VermeerschDepartment of Laboratory of Laboratory Medicine, University Hospitals Leuven, Louvain, Belgium.
Hans PottelDepartment of Public Health and Primary Care, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.
Djalila MekahliPKD Research Group, Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium. djalila.mekahli@uzleuven.be.ORCID http://orcid.org/0000-0003-0954-6088
KU Leuven · BEErasmus MC · NLUniversity of Liège · BEVIB-KU Leuven Center for Brain & Disease Research · BEVrije Universiteit Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundYoung autosomal dominant polycystic kidney disease (ADPKD) patients are becoming the new target population for the development of new treatment options. Determination of a reliable equation for estimated glomerular filtration rate (eGFR) from early stages is needed with the promising potential interventional therapies.

methodsProspective and longitudinal study on a cohort of 68 genotyped ADPKD patients (age range 0-23 years) with long-term follow-up. Commonly used equations for eGFR were compared for their relative performance.

resultsThe revised Schwartz formula (CKiD) showed a highly significant decline in eGFR with aging (- 3.31 mL/min/1.73 m

conclusionsThe most widely used methods to calculate eGFR in ADPKD children (CKiD and CKiDU25 equations) were associated with unexpected age or sex differences. The FAS equations were age- and sex-independent in our cohort. Hence, the switch from the CKiD to CKD-EPI equation at the transition from pediatric to adult care causes implausible jumps in eGFR, which could be misinterpreted. Having reliable methods to calculate eGFR is indispensable for clinical follow-up and clinical trials. A higher resolution version of the Graphical abstract is available as Supplementary information.

Indexed as

Polycystic Kidney, Autosomal DominantRenal Insufficiency, ChronicTransition to Adult CareAdolescentAdultChildChild, PreschoolCreatinineFemaleGlomerular Filtration RateHumansInfantInfant, NewbornLongitudinal StudiesMaleProspective StudiesCreatinineADPKDCreatinineCystatin cEstimated glomerular filtration rateHyperfiltrationMeasured glomerular filtration rate

Identifiers

PMID36939917
OpenAlexW4327900032

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.