Ikerketa metabolomikoak haurretan gertatzen den giltzurrun gutxiegitasun kronikoaren diagnostikorako biomarkatzaile berrien identifikazioan

  1. Benito, Sandra 1
  2. Unceta, Nora 1
  3. Sánchez-Ortega, Alicia 1
  4. Gómez-Caballero, Alberto 1
  5. Goicolea, M. Aránzazu 1
  6. Barrio, Ramón J. 1
  1. 1 Euskal Herriko Unibertsitatea (UPV/EHU)
Journal:
Ekaia: Euskal Herriko Unibertsitateko zientzi eta teknologi aldizkaria

ISSN: 0214-9001

Year of publication: 2020

Issue: 37

Pages: 65-81

Type: Article

DOI: 10.1387/EKAIA.20859 DIALNET GOOGLE SCHOLAR lock_openOpen access editor

More publications in: Ekaia: Euskal Herriko Unibertsitateko zientzi eta teknologi aldizkaria

Abstract

The assessment of chronic kidney disease (CKD) is performed by means of glomerular filtration rate (GFR), which is calculated from equations using serum creatinine concentration. However, serum creatinine concentration changes according to several factors, and this might endanger CKD diagnosis, especially in early stages of the disease. In addition to metabolic and cardiovascular complications, CKD is related to growth complications and malnutrition. All of these complications lead to a 30 times higher mortality rate in paediatrics suffering from advanced CKD compared to healthy counterparts. Overall, the existence of biomarkers for a defined disease allows earlier diagnosis as well as better response. For that reason, comprehensive research has been performed in adults suffering from CKD aimed at finding new biomarkers, however only a few studies are available in paediatrics with CKD so far, and there is a need for new biomarkers in this population. For that purpose, following targeted and untargeted metabolomics approaches seven potential biomarkers have been found which could be useful for paediatric CKD by comparing metabolic profiles. The use of these metabolites in addition to creatinine enables better differentiation of paediatrics with CKD and control ones, unlike just creatinine itself.