RPG was analysed within 2 hours of sample collection by
hexokinase method while HbA1c was analysed using Tina-quant method on a fully automated chemistry analyser (Roche Modular P800).
All glucose measurements in patient samples were performed using the
hexokinase method.
FPG was analyzed within 2 hours of sample collection by
hexokinase method while serum Mg was analyzed using xylidyl blue methodon ADVIA 1800(r) siemens clinical chemistry auto-analyzer.
Plasma glucose was measured using an enzymatic
hexokinase method.
Glucose analysis was performed in a central laboratory using a
hexokinase method on a Siemens Advia 1800.
Blood glucose was estimated by
hexokinase method on Olympus AU2700 analyzer.
Glucose was measured according to the
hexokinase method.
Glucose was analyzed by
hexokinase method on a random access clinical chemistry analyzer (Hitachi-902).
Fasting glucose triglyceride and high- density lipoprotein (HDL) levels were analysed with a Roche C-501 (Tokyo Japan) by using the
hexokinase method (glucose) and homogeneous colorimetric enzyme test (triglyceride and HDL).
Serum glucose level was measured using a commercial kit (Pars Azmoon Company, Tehran, Iran) based on the
hexokinase method.
We used the modified
hexokinase method to measure serum glucose levels at the University of Missouri Diabetes Diagnostic Laboratory (Columbia, MO, USA).
Blood urea nitrogen, glucose, albumin, creatinine and total protein concentrations were analyzed using an automatic blood analyzer (Express Plus, Ciba-Corning, CA, USA) according to the urease method of Rocch-Ramel (1967), the
hexokinase method of Farrance (1987), the bromocresol green method of Doumas et al.
