Expanded newborn screening using tandem mass spectrometry

被引:19
作者
Roscher, AA [1 ]
Fingerhut, R [1 ]
Liebl, B [1 ]
Olgemöller, B [1 ]
机构
[1] Univ Munich, Dr Von Haunerschen Kinderspital, Kinderklin & Kinderpoliklin, D-80337 Munich, Germany
关键词
newborn screening; tandem mass spectrometry; bavarian model program;
D O I
10.1007/s001120170015
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Tandem mass spectrometry is a promising new screening technology. It enables to screen simultaneously within the same analytical run not only for phenylketonuria but also for a wide range of other treatable disorders in the metabolism of amino acids, organic acids and fatty acids. The high potential for an additional preventive benefit must be weighed against risks that might arise from lack of quality assured and premature technology application such as late screening, lack of intervention measures or high false positive rates. Here we describe the technical and medical prerequisites for technology introduction within a Bavarian model program and the results on > 300.000 newborns accumulated since 1999. At overall low recall rates a cumulative detection rate of 1:2.700 was achieved. In particular the high frequency in the recognition of fatty oxidation disorders (1:8.500) is expected to provide a high preventive effect.
引用
收藏
页码:1297 / +
页数:6
相关论文
共 17 条
[1]  
Chace DH, 1998, CLIN CHEM, V44, P2405
[2]  
Fingerhut R, 2001, CLIN CHEM, V47, P1763
[3]   Electrospray and tandem mass spectrometry in biochemistry [J].
Griffiths, WJ ;
Jonsson, AP ;
Liu, SY ;
Rai, DK ;
Wang, YQ .
BIOCHEMICAL JOURNAL, 2001, 355 :545-561
[4]   Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA:: carboxylase deficiency [J].
Holzinger, A ;
Röschinger, W ;
Lagler, F ;
Mayerhofer, PU ;
Lichtner, P ;
Kattenfeld, T ;
Thuy, L ;
Nyhan, WL ;
Koch, HG ;
Muntau, AC ;
Roscher, AA .
HUMAN MOLECULAR GENETICS, 2001, 10 (12) :1299-1306
[5]   MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY - CLINICAL COURSE IN 120 AFFECTED CHILDREN [J].
IAFOLLA, AK ;
THOMPSON, RJ ;
ROE, CR .
JOURNAL OF PEDIATRICS, 1994, 124 (03) :409-415
[6]  
LABERGE C, 1990, AM J HUM GENET, V47, P325
[7]  
Levy HL, 1998, CLIN CHEM, V44, P2401
[8]   The bavarian newborn screening model -: Concept and first results [J].
Liebl, B ;
Fingerhut, R ;
Röschinger, W ;
Muntau, A ;
Knerr, I ;
Olgemöller, B ;
Zapf, A ;
Roscher, AA .
GESUNDHEITSWESEN, 2000, 62 (04) :189-195
[9]  
LIEBL B, 2001, IN PRESS PREV MED
[10]   High prevalence of the 1278T mutation of the human cystathionine β-synthase detected by a novel screening application [J].
Linnebank, M ;
Homberger, A ;
Junker, R ;
Nowak-Goettl, U ;
Harms, E ;
Koch, HG .
THROMBOSIS AND HAEMOSTASIS, 2001, 85 (06) :986-988