Evidence for shrunken pore syndrome in children.
Cystatin C
creatinine
shrunken pore syndrome
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
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