Naslov
Serum paraoxonase activities in endemic nephropathy patients on long-term hemodialysis

Autori
Tadijanović, Milena ; Rekić, Branka ; Simeon-Rudolf, Vera ; Baričić, Martin ; Juretić, Dubravka ; Miškić, B.

Izvornik
Collegium Antropologicum (0350-6134) 30:suppl. 1 (2006);

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, kongresno priopcenje, znanstveni

Ključne riječi
paraoxonase; long-term hemodialsis; endemic nephropathy

Sažetak
Aim To determine whether paraoxonase activity, paraoxonase phenotype and lipid status are altered in endemic nephropathy patients on long-term hemodialsis treatment as compared to healthy population. Materials and Methods Endemic nephropathy patients (n=31) and control subjects (n=145) were from the area of Slavonski Brod, Croatia. Paraoxon was used as a substrate for measuring basal and sodium chloride-stimulated (NaCl-stimulated) paraoxonase activity, and phenylacetate for measuring arylesterase activity. The double substrate method was used to assign phenotypes. Cholesterol, triglycerides, and high-density lipoprotein cholesterol (HDL-cholesterol) were determined by methods routinely used in medical-biochemical laboratories. Results are expressed as median values and tested by Mann-Whitney rank sum test. The values p<0.05 .were considered significant. Results Basal and NaCl-stimulated paraoxonase activity as well as arylesterase activity were significantly lower in the patient group compared to controls ; 68% (p<0.001), 71% (p<0.001), and 58%(p<0.001), respectively. The distribution of paraoxonase phenotypes in patient group and controls was as follow: AA 45% and 39%, AB 37% and 48%, BB 185 and 13%, respectively. Cholesterol and HDL-cholesterol were significantly decreased (87%, p<0.001 and 71% p<0.001, respectively), whereas triglycerides were significantly increased (195 %, p<0.001) in the patient group compared to control median value. Conclusion Endemic nephropaty patients on long term hemodialysis have decreased paraoxonase /arylesterase activity, which might indicate a greater risk of premature atherogenesis.

Izvorni jezik
Engleski

Znanstvena područja
Farmacija

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