Galactitol and galactonate in red blood cells of children with the Duarte/galactosemia genotype

被引:16
作者
Ficicioglu, C
Yager, C
Segal, S
机构
[1] Univ Penn, Sch Med, Dept Pediat, Childrens Hosp Philadelphia,Sect Biochem Genet, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Pediat, Childrens Hosp Philadelphia,Metab Res Lab, Philadelphia, PA 19104 USA
关键词
galactitol; galactonate; galactose-1-phosphate; duarte mutation; newborn screening; Galactosemia;
D O I
10.1016/j.ymgme.2004.11.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We measured galactitol, galactonate, and galactose-1-phosphate in the red blood cell (RBC) to elucidate the biochemical phenotype of infants with a Duarte/galactosemia (D/G) genotype by isotope dilution GC/MS. The RBC galactonate, galactitol and Gal-1-P were quantified in 14 D/G newborns on a lactose containing formula or breast milk, eight D/G newborns on a galactose-free formula, and 18 D/G children between 1 and 2 years of age that were on a regular diet. The results were compared with those of nongalactosemic subjects of comparable age. In the D/G newborns on regular formula/breast milk, the levels of RBC galactitol, galactonate, and Gal-1-P were significantly higher than those of D/G newborns on diet treatment and non-galactosemic newborns. There was no difference in the levels of RBC galactitol, galactonate, and Gal-1-P between D/G newborns on a lactose-restricted diet and the control group. There appears to be two different responses to dietary galactose intake in D/G children. The first group of D/G children placed on a regular diet after a year of lactose restriction had higher RBC galactitol, galactonate levels than those of non-galactosemic children. The mean level of RBC galactonate was higher and the mean value of RBC galactitol was as high as that of galactosemic (G/G) patients on diet treatment. The second group of D/G children on a regular diet had normal levels of RBC galactitol and galactonate. The levels of RBC Gal-1-P were normal in both groups of D/G patients. The alternative pathway products may reflect galactose intake better than RBC Gal-1-P in D/G children. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:152 / 159
页数:8
相关论文
共 22 条
[1]   The rate of de novo galactose synthesis in patients with galactose-1-phosphate uridyltransferase deficiency [J].
Berry, GT ;
Moate, PJ ;
Reynolds, RA ;
Yager, CT ;
Ning, C ;
Boston, RC ;
Segal, S .
MOLECULAR GENETICS AND METABOLISM, 2004, 81 (01) :22-30
[2]   Elevation of erythrocyte redox potential linked to galactonate biosynthesis: Elimination by tolrestat [J].
Berry, GT ;
Wehrli, S ;
Reynolds, R ;
Palmieri, M ;
Frangos, M ;
Williamson, JR ;
Segal, S .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1998, 47 (11) :1423-1428
[3]  
BLAIR A, 1960, J LAB CLIN MED, V55, P959
[4]   Identification of galactitol and galactonate in red blood cells by gas chromatography/mass spectrometry [J].
Chen, J ;
Yager, CT ;
Reynolds, RA ;
Segal, S .
CLINICA CHIMICA ACTA, 2002, 322 (1-2) :37-41
[5]  
Chen J, 2002, CLIN CHEM, V48, P604
[6]   GALACTOSE CONVERSION TO D-XYLULOSE - AN ALTERNATE ROUTE OF GALACTOSE METABOLISM [J].
CUATRECASAS, P ;
SEGAL, S .
SCIENCE, 1966, 153 (3735) :549-+
[7]   Analysis of common mutations in the galactose-1-phosphate uridyl transferase gene - New assays to increase the sensitivity and specificity of newborn screening for galactosemia [J].
Dobrowolski, SF ;
Banas, RA ;
Suzow, JG ;
Berkley, M ;
Naylor, EW .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2003, 5 (01) :42-47
[8]  
DONNELL GN, 1963, PEDIATRICS, V31, P802
[9]  
ELSAS LJ, 1994, AM J HUM GENET, V54, P1030
[10]  
GITZELMANN R, 1974, EUR J CLIN INVEST, V4, P79, DOI 10.1111/j.1365-2362.1974.tb00376.x