Galactitol and galactonate in red blood cells of galactosemic patients

Molecular Genetics and Metabolism
2003.0

Abstract

The red blood cell (RBC) concentration of galactitol and galactonate was measured in 27 patients with galactose-1-phosphate uridyltransferase (GALT) deficiency galactosemia and 19 non-galactosemic subjects by a newly devised isotope dilution gas chromatography/mass spectrometry (GC/MS) method. The method utilizing UL[13C]galactitol and UL[13C]galactonate was reproducible with excellent precision and recovery of 99%. The RBC galactitol in galactosemic patients on galactose-restricted diets averaged 5.98+/-1.2 microM (M+/-SD) with a range of 3.54-8.81 microM. The mean in non-galactosemic patients was 0.73+/-0.31 microM with a range of 0.29-1.29 microM. The mean of RBC galactonate in the same galactosemic patients was 4.16+/-1.32 microM (M+/-SD) with a range of 0.68-6.47, while the mean in non-galactosemic subjects was 1.94+/-0.96 (M+/-SD) with a range of 0.69-3.84. In galactosemic RBC the galactitol was higher than galactonate while this was reversed in non-galactosemic cells. RBC galactose-1-phosphate (Gal-1-P) measured at the same time as galactitol and galactonate was 30 times the level of the other two metabolites. There was no relationship between RBC Gal-1-P and galactitol or galactonate. The ability to measure all three galactose metabolites in the same procedure offers the possibility of augmented monitoring of the galactose metabolic status of patients. The measurement of RBC galactitol and galactonate presents a new means of characterizing galactosemic patients and their levels monitored over time may provide new insight in the development of long-term complications observed in afflicted patients.

Knowledge Graph

Similar Paper

Galactitol and galactonate in red blood cells of galactosemic patients
Molecular Genetics and Metabolism 2003.0
Simultaneous determination of gluconolactone, galactonolactone and galactitol in urine by reversed-phase liquid chromatography: application to galactosemia
Journal of Chromatography B: Biomedical Sciences and Applications 1991.0
Characterization of retinyl beta-glucuronide in human blood
The American Journal of Clinical Nutrition 1989.0
Sensitivity and specificity of free and total glutaric acid and 3‐hydroxyglutaric acid measurements by stable‐isotope dilution assays for the diagnosis of glutaric aciduria type I
Journal of Inherited Metabolic Disease 1999.0
Ribose-5-Phosphate Isomerase Deficiency: New Inborn Error in the Pentose Phosphate Pathway Associated with a Slowly Progressive Leukoencephalopathy
The American Journal of Human Genetics 2004.0
Volatile substances in blood serum: Profile analysis and quantitative determination
Journal of Chromatography A 1977.0
A new galactosyl transferase inhibitor
Bioorganic & Medicinal Chemistry Letters 1993.0
A gas chromatographic—mass spectrometric study of profiles of volatile metabolites in hepatic encephalopathy
Journal of Chromatography B: Biomedical Sciences and Applications 1981.0
Inhibitory Effect of Gallic Acid and Its Esters on 2,2′-Azobis(2-amidinopropane)hydrochloride (AAPH)-Induced Hemolysis and Depletion of Intracellular Glutathione in Erythrocytes
Journal of Agricultural and Food Chemistry 2010.0
3‐Hydroxyglutarate excretion is increased in ketotic patients: Implications for glutaryl‐CoA dehydrogenase deficiency testing
Journal of Inherited Metabolic Disease 2002.0