Evidence for shrunken pore syndrome in children.


Journal

Scandinavian journal of clinical and laboratory investigation
ISSN: 1502-7686
Titre abrégé: Scand J Clin Lab Invest
Pays: England
ID NLM: 0404375

Informations de publication

Date de publication:
Feb 2020
Historique:
pubmed: 23 11 2019
medline: 10 3 2021
entrez: 23 11 2019
Statut: ppublish

Résumé

The link between cystatin C and mortality independent of glomerular filtration rate (GFR) in adults has prompted the "Shrunken Pore Syndrome" (SPS) hypothesis, where high serum cystatin C with normal creatinine is explained by smaller glomerular pores, through which creatinine can pass freely, while the larger cystatin C, beta-trace protein (BTP) and pro-inflammatory molecules are retained. This study set out to apply the definition of SPS to children. In 294 children who underwent inulin clearance (Cin) test, serum creatinine, cystatin C and BTP were measured. For all three markers eGFR

Identifiants

pubmed: 31755786
doi: 10.1080/00365513.2019.1692231
doi:

Substances chimiques

Biomarkers 0
Cystatin C 0
Lipocalins 0
Creatinine AYI8EX34EU
Intramolecular Oxidoreductases EC 5.3.-
prostaglandin R2 D-isomerase EC 5.3.99.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

32-38

Auteurs

Emil den Bakker (E)

Department of Pediatrics, Amsterdam University Medical Center, Amsterdam, the Netherlands.

Reinoud Jbj Gemke (RJ)

Department of Pediatrics, Amsterdam University Medical Center, Amsterdam, the Netherlands.

Joanna Ae van Wijk (JA)

Department of Pediatrics, Amsterdam University Medical Center, Amsterdam, the Netherlands.

Isabelle Hubeek (I)

Department of Clinical Chemistry, Amsterdam University Medical Center, Amsterdam, the Netherlands.

Birgit Stoffel-Wagner (B)

Department of Clinical Chemistry and Clinical Pharmacology, University Clinics, Bonn, Germany.

Arend Bökenkamp (A)

Department of Pediatrics, Amsterdam University Medical Center, Amsterdam, the Netherlands.

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Classifications MeSH