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Uridine correlates with the concentration of fructosamine and HbA1c in children with type 1 diabetes.

Authors :
Dudzinska W
Source :
Acta paediatrica (Oslo, Norway : 1992) [Acta Paediatr] 2011 May; Vol. 100 (5), pp. 712-6. Date of Electronic Publication: 2011 Feb 25.
Publication Year :
2011

Abstract

Aim: Treating uridine as a product of UTP degradation and hypoxanthine as a degradation product of ATP, we assessed the concentration of uridine and hypoxanthine in the blood of children with newly diagnosed type 1 diabetes. We also sought to define the relationship between indicators of the degree of metabolic control of diabetes (fructosamine, HbA1c) and the concentration of the tested catabolites.<br />Methods: This study was carried out on 33 children aged 12.26 ± 4.49 with newly diagnosed type 1 diabetes during their first hospitalization. The concentration of uridine and hypoxanthine was determined by high-performance liquid chromatography (HPLC).<br />Results: The results showed significantly elevated levels of hypoxanthine and uridine in the blood. We further show that blood uridine level is associated with purine metabolism and hyperglycaemia, and we demonstrate a significant positive correlation between the concentration of uridine and (i) the percentage of HbA1c and (ii) fructosamine levels, which indicate the role of hyperglycaemia in the pathogenesis of pyrimidine nucleotide metabolism in type 1 diabetes prior to diagnosis.<br />Conclusion: The results confirm the existence of a relationship between the degree of metabolic control of diabetes and pyrimidine metabolism. Presumably, the analysis of uridine could be used as an adjunct marker of the severity of diabetic complications in newly diagnosed patients.<br /> (© 2011 The Author/Acta Paediatrica © 2011 Foundation Acta Paediatrica.)

Details

Language :
English
ISSN :
1651-2227
Volume :
100
Issue :
5
Database :
MEDLINE
Journal :
Acta paediatrica (Oslo, Norway : 1992)
Publication Type :
Academic Journal
Accession number :
21470306
Full Text :
https://doi.org/10.1111/j.1651-2227.2011.02146.x