Newborn mass screening and selective screening using electrospray tandem mass spectrometry in Japan

被引:131
作者
Shigematsu, Y [1 ]
Hirano, S
Hata, I
Tanaka, Y
Sudo, M
Sakura, N
Tajima, T
Yamaguchi, S
机构
[1] Fukui Med Univ, Sch Nursing, Dept Hlth Sci, Matsuoka, Fukui 9101193, Japan
[2] Fukui Med Univ, Sch Med, Dept Pediat, Fukui, Japan
[3] Fukui Med Univ, Cent Res Labs, Fukui, Japan
[4] Fac Med, Dept Pediat, Minami Ku, Hiroshima 7348551, Japan
[5] Shimane Med Univ, Dept Pediat, Izumo, Shimane 6938501, Japan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2002年 / 776卷 / 01期
基金
日本学术振兴会;
关键词
newborn mass screening; inherited metabolic disorders;
D O I
10.1016/S1570-0232(02)00077-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Electrospray tandem mass spectrometry was applied to detect a series of inherited metabolic disorders during a newborn-screening pilot study and a selective screening in Japan. In our mass screening of 102 200 newborns, five patients with propionic acidemia, two with methylmalonic acidemia, two with medium-chain acyl-CoA dehydrogenase deficiency, three with citrullinemia type II, and one with phenylketonuria were identified. In a selective screening of 164 patients with symptoms mainly related to hypoglycemia and/or hyperammonemia, 12 with fatty acid oxidation disorders and six with other disorders were found. The results indicated the importance of newborn screening using this technology in Japan. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:39 / 48
页数:10
相关论文
共 25 条
[1]  
Chace DH, 1997, CLIN CHEM, V43, P2106
[2]   Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry [J].
Clayton, PT ;
Doig, M ;
Ghafari, S ;
Meaney, C ;
Taylor, C ;
Leonard, JV ;
Morris, M ;
Johnson, AW .
ARCHIVES OF DISEASE IN CHILDHOOD, 1998, 79 (02) :109-115
[3]  
FRERMAN EF, 1985, BIOCH MED, V3, P38
[4]  
Greenstein J. P., 1961, Chemistry of the Amino Acids
[5]  
Hisashige A, 1994, Int J Technol Assess Health Care, V10, P382
[6]   The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein [J].
Kobayashi, K ;
Sinasac, DS ;
Iijima, M ;
Boright, AP ;
Begum, L ;
Lee, JR ;
Yasuda, T ;
Ikeda, S ;
Hirano, R ;
Terazono, H ;
Crackower, MA ;
Kondo, I ;
Tsui, LC ;
Scherer, SW ;
Saheki, T .
NATURE GENETICS, 1999, 22 (02) :159-163
[7]   Diagnosis of inborn errors of metabolism using filter paper urine, urease treatment, isotope dilution and gas chromatography-mass spectrometry [J].
Kuhara, T .
JOURNAL OF CHROMATOGRAPHY B, 2001, 758 (01) :3-25
[8]  
Marsden D., 2000, Journal of Inherited Metabolic Disease, V23, P14
[9]  
Marsden D., 2000, Journal of Inherited Metabolic Disease, V23, P15
[10]   Automated tandem mass spectrometry for mass newborn screening for disorders in fatty acid, organic acid, and amino acid metabolism [J].
Naylor, EW ;
Chace, DH .
JOURNAL OF CHILD NEUROLOGY, 1999, 14 :S4-S8