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Quantitative determination of succinylacetone in dried blood spots for newborn screening of tyrosinemia type I
被引:52
作者:
Magera, MJ
Gunawardena, ND
Hahn, SH
Tortorelli, S
Mitchell, GA
Goodman, SI
Rinaldo, P
Matern, D
[1
]
机构:
[1] Mayo Clin, Coll Med, Biochem Genet Lab, Rochester, MN 55905 USA
[2] Hop St Justine, Dept Pediat, Montreal, PQ H3T 1C5, Canada
[3] Univ Colorado, Hlth Sci Ctr Fitzsimons, Biochem Genet Lab, Aurora, CO 80045 USA
关键词:
tyrosinemia type I;
fumarylacetoacetate hydrolase deficiency;
succinylacetone;
newborn screening;
tandem mass spectrometry;
dried blood spot;
D O I:
10.1016/j.ymgme.2005.12.005
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: Tyrosinemia type I (TYR 1) is a severe disorder causing early death if left untreated. While tyrosine can be determined in dried blood spots (DBS), it is not a specific marker for TYR 1 and most often associated with benign transient tyrosinemia of the newborn. Succinylacetone (SUAC) is a specific marker for TYR 1 but not detectable by routine newborn screening. We developed a new assay that determines SUAC in DBS by liquid-chromatography tandem mass spectrometry (LC-MS/MS). Methods: Whole blood is eluted from a 3/16-in. DBS by an aqueous solution containing deuterium labeled SUAC as internal standard (IS). SUAC and IS are oximated, then extracted, butylated, and analyzed by LC-MS/MS. Quantitation is from SUAC spiked calibrator DBS over the range 0-200 mu M using selected reaction monitoring of transitions m/z 212 to 156 and m/z 214 to 140 for SUAC and IS, respectively. Analysis time is 5 min. To assess the effectiveness of a two-tier screening approach for TYR 1 we applied this assay to our newborn screening program over the last 15 months. Results: The intra-assay precision was determined for three different levels of SUAC (5, 20, and 50 mu mol/L) and the CV calculated to be 4.7, 2.6, and 3.1%, respectively (n = 5). Inter-assay precision CVs were 12.7, 8.2, and 7.8%, respectively on the same samples. SUAC levels in DBS from 10 confirmed TYR 1 cases not treated with 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC) were clearly abnormal (16-150 mu mol/L; mean: 61 mu mol/L; controls: < 5 mu mol/L). Over a 15-month period, SUAC was determined in newborn screening samples with elevated tyrosine concentrations when applying different cut off values until it was settled at 150 mu mol/L. No case of TYR I was detected in 124,780 newborns tested. Conclusion: We have developed a new LC-MS/MS based method for the determination of SUAC in DBS. This assay has the potential to significantly reduce the number of false positive results in newborn screening for TYR 1 and can also be used for the laboratory follow up of patients treated for TYR 1. (c) 2005 Elsevier Inc. All rights reserved.
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页码:16 / 21
页数:6
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