Methylglyoxal-derivative advanced glycation endproducts : detection by competitive immunofluorometric assay and quantifying in serum and urine (CROSBI ID 150852)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Turk, Zdenka ; Vrdoljak, Anto ; Mišur, Irena ; Trešćec, Anđa ; Benko, Bojan
engleski
Methylglyoxal-derivative advanced glycation endproducts : detection by competitive immunofluorometric assay and quantifying in serum and urine
Advanced glycation endproducts (AGE) are a family of heterogeneous chemical structures formed on the host protein in the conditions of carbonyl or oxidative stress. Among AGE precursors, methylglyoxal (MG) is considered as one of the key intermediates. In the current study, we describe and evaluate a solid phase time-resolved fluoroimmunoassay (DELFIA) based on the competitive reaction between MG-AGE antibody and competitive antigen for detecting MG-adducts in serum and urine. The fluorometry assay was validated by comparison with previously established ELISA. The mean concentration of MG-adducts assayed by competitive DELFIA in sera of diabetic patients was higher in comparison to non-diabetic controls: 331 144 mgEq/mL (range 103-720) vs 197 51 mgEq/L (range 117-287) ; one-way ANOVA (p<0.014). In diabetic subjects, urinary excretion of MG-adducts significantly exceeded the mean level measured in controls (77.1 86.1 mgEq/L, range 0-250 vs 33.5 37.5 mgEq/L, range 0-68 ; p<0.003). MG-adducts in urine were low and undetectable in 8 of 28 control subjects and 2 of 66 diabetics. The percentage recovery of MG-adduct added in the same concentration to control and diabetic pool sera showed under-recovery in the latter. Comparison of total AGE level and the amount of MG-adducts revealed MG-derivatives to account for 37% of the heterogeneous structure commonly termed AGE. The fluoroimmunoassay for MG-derivative AGE evaluated can be utilized on biomonitoring of MG-adducts in serum and its urinary excretion. Competitive DELFIA assay was found to be substantially more sensitive than standard ELISA and to have a wider dynamic range, while sharing similar quenching attributes.
advanced glycation endproduct; methylglyoxal; enzyme-linked immunoassay;
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano