Quantitative acylcarnitine profiling in fibroblasts using [U-13C] palmitic acid:: an improved tool for the diagnosis of fatty acid oxidation defects

被引:72
|
作者
Ventura, FV
Costa, CG
Struys, EA
Ruiter, J
Allers, P
Ijlst, L
de Almeida, T
Duran, M
Jakobs, C
Wanders, RJA
机构
[1] Univ Hosp Amsterdam, AMC, Dept Clin Biochem, Lab Genet Metab Dis, NL-1105 AZ Amsterdam, Netherlands
[2] Free Univ Amsterdam Hosp, Dept Clin Chem, Metab Unit, NL-1081 HV Amsterdam, Netherlands
[3] Univ Childrens Hosp Het Wilhelmina Kinderziekenhu, NL-3501 CA Utrecht, Netherlands
[4] Univ Lisbon, Fac Farm, Ctr Patogenese Mol, P-1600 Lisbon, Portugal
关键词
diagnosis of mitochondrial fatty acid beta-oxidation disorders; inborn errors of metabolism; in vitro acylcarnitines;
D O I
10.1016/S0009-8981(98)00188-0
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
A method was developed for the investigation of mitochondrial fatty acid P-oxidation in cultured fibroblasts. Monolayer cultures were incubated without foetal calf serum with commercially available [U-C-13] palmitic acid and L-carnitine for 96 h. The acylcarnitines produced by the cells were extracted from the cell suspension and analysed either by quantitative stable isotope dilution gas chromatography chemical ionization mass spectrometry, or by fast atom bombardment mass spectrometry. Characteristic acylcarnitine profiles were obtained for all the different enzyme deficiencies investigated, with the exception of carnitine palmitoyltransferase II deficiency and carnitine/acylcarnitine carrier deficiency which showed similar patterns. Comparison between this method and the H-3-myristate and H-3-palmitate tritium release assays revealed that the method described here is superior, allowing unequivocal identification of patients. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1 / 17
页数:17
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