Disease-related metabolites in culture medium of fibroblasts from patients with D-2-hydroxyglutaric aciduria, L-2-hydroxyglutaric aciduria, and combined D/L-2-hydroxyglutaric aciduria

被引:17
作者
Struys, EA [1 ]
Verhoeven, NM [1 ]
Roos, B [1 ]
Jakobs, C [1 ]
机构
[1] Vrije Univ Amsterdam, Ctr Med, Dept Clin Chem, Metab Unit, NL-1081 HV Amsterdam, Netherlands
关键词
D O I
10.1373/49.7.1133
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: D-2-Hydroxyglutaric aciduria (D-2-HGA), L-2-hydroxyglutaric aciduria (L-2-HGA), and the combined D/L-2-hydroxygiutaric aciduria (D/L-2-HGA) are poorly understood organic acidurias. To investigate the usefulness of cultured human skin fibroblasts for both diagnostic and research purposes, we measured disease-related metabolites in the cell culture Medium. Methods: We measured D-2-hydroxyglutarate (D-2-HG), L-2-hydroxyglitarate (L-2-HG), succinate, 2-ketoglutarate, and citrate in fibroblast cell medium by stable-isotope-dilution gas chromatography-mass spectrometry and glutamine, glutamic acid, and lysine with an amino acid analyzer. We used six cell lines from patients with D-2-HGA, two from patients with L-2-HGA, three from patients with D/L-2-HGA, and seven control cell lines. Culture medium was analyzed After a 96-h incubation period. Results: Culture media from cell lines from D-2-HGA patients contained D-2-HG at concentrations 5- to 30-fold higher than media from controls, whereas the concentration of L-2-HG in media was not increased. Media from L-2-HGA cell lines showed a fivefold increase in L-2-HG compared with controls. Media containing fibroblasts from D/L-2-HGA patients contained moderately increased amounts of both D-2-HG and L-2-HG. For all cell lines, succinate concentrations in the blank medium were higher than after 96 h of incubation with the exception of two of three D/L-2-HGA cell lines. Media of D-2-HGA cell lines had 2-ketoglutarate concentrations that were 40% of that for controls. Glutamic acid concentrations in media of these cell lines were 60% lower than in controls. Conclusions: Cell culture media from fibroblasts from patients with D-2-HGA, L-2-HGA, or D/L-2-HGA contain increased amounts the corresponding 2-HGs, demonstrating the suitability of fibroblasts for both diagnosis of and research concerning 2-HGAs. (C) 2003 American Association for Clinical Chemistry.
引用
收藏
页码:1133 / 1138
页数:6
相关论文
共 17 条
[1]   L-2-HYDROXYGLUTARIC ACIDEMIA - CLINICAL AND BIOCHEMICAL FINDINGS IN 12 PATIENTS AND PRELIMINARY-REPORT ON L-2-HYDROXYACID DEHYDROGENASE [J].
BARTH, PG ;
HOFFMANN, GF ;
JAEKEN, J ;
WANDERS, RJA ;
DURAN, M ;
JANSEN, GA ;
JAKOBS, C ;
LEHNERT, W ;
HANEFELD, F ;
VALK, J ;
SCHUTGENS, RBH ;
TREFZ, FK ;
HARTUNG, HP ;
CHAMOLES, NA ;
SFAELLO, Z ;
CARUSO, U .
JOURNAL OF INHERITED METABOLIC DISEASE, 1993, 16 (04) :753-761
[2]   L-2-HYDROXYGLUTARIC ACIDEMIA - A NOVEL INHERITED NEUROMETABOLIC DISEASE [J].
BARTH, PG ;
HOFFMANN, GF ;
JAEKEN, J ;
LEHNERT, W ;
HANEFELD, F ;
VANGENNIP, AH ;
DURAN, M ;
VALK, J ;
SCHUTGENS, RBH ;
TREFZ, FK ;
REIMANN, G ;
HARTUNG, HP .
ANNALS OF NEUROLOGY, 1992, 32 (01) :66-71
[3]  
Chalmers R A, 1980, J Inherit Metab Dis, V3, P11, DOI 10.1007/BF02312516
[4]   L-2-hydroxyglutaric aciduria: Clinical heterogeneity versus biochemical homogeneity in a sibship [J].
de Klerk, JBC ;
Huijmans, JGM ;
Stroink, H ;
Robben, SGF ;
Jakobs, C ;
Duran, M .
NEUROPEDIATRICS, 1997, 28 (06) :314-317
[5]  
Duran M, 1980, J Inherit Metab Dis, V3, P109, DOI 10.1007/BF02312543
[6]   STABLE-ISOTOPE DILUTION ANALYSIS OF D-2-HYDROXYGLUTARIC AND L-2-HYDROXYGLUTARIC ACID - APPLICATION TO THE DETECTION AND PRENATAL-DIAGNOSIS OF D-2-HYDROXYGLUTARIC AND L-2-HYDROXYGLUTARIC ACIDEMIAS [J].
GIBSON, KM ;
TENBRINK, HJ ;
SCHOR, DSM ;
KOK, RM ;
BOOTSMA, AH ;
HOFFMANN, GF ;
JAKOBS, C .
PEDIATRIC RESEARCH, 1993, 34 (03) :277-280
[7]   D-2-HYDROXYGLUTARIC ACIDURIA IN A NEWBORN WITH NEUROLOGICAL ABNORMALITIES - A NEW NEUROMETABOLIC DISORDER [J].
GIBSON, KM ;
CRAIGEN, W ;
HERMAN, GE ;
JAKOBS, C .
JOURNAL OF INHERITED METABOLIC DISEASE, 1993, 16 (03) :497-500
[8]  
Jones PM, 2001, CLIN CHEM, V47, P1190
[9]  
KAUFMAN EE, 1988, J BIOL CHEM, V263, P16872
[10]   Combined D-2-and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy:: A third biochemical variant of 2-hydroxyglutaric aciduria? [J].
Muntau, AC ;
Röschinger, W ;
Merkenschlager, A ;
van der Knaap, MS ;
Jakobs, C ;
Duran, M ;
Hoffmann, GF ;
Roscher, AA .
NEUROPEDIATRICS, 2000, 31 (03) :137-140