Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders

被引:146
|
作者
Gelb, Michael H. [1 ]
Turecek, Frantisek
Scott, C. Ron
Chamoles, Nestor A.
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[2] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[3] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[4] Lab Neurochem, RA-1425 Buenos Aires, DF, Argentina
[5] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
关键词
D O I
10.1007/s10545-006-0265-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tandem mass spectrometry is currently used in newborn screening programmes to quantify the level of amino acids and acylcarnitines in dried blood spots for detection of metabolites associated with treatable diseases. We have developed assays for lysosomal enzymes in rehydrated dried blood spots in which a set of substrates is added and the set of corresponding enzymatic products are quantified using tandem mass spectrometry with the aid of mass-differentiated internal standards. We have developed a multiplex assay of the set of enzymes that, when deficient, cause the lysosomal storage disorders Fabry, Gaucher, Hurler, Krabbe, Niemann-Pick A/B and Pompe diseases. These diseases were selected because treatments are now available or expected to emerge shortly. The discovery that acarbose is a selective inhibitor of maltase glucoamylase allows the Pompe disease enzyme, acid alpha-glucosidase, to be selectively assayed in white blood cells and dried blood spots. When tested with dried blood spots from 40 unaffected individuals and 10-12 individuals with the lysosomal storage disorder, the tandem mass spectrometry assay led to the correct identification of the affected individuals with 100% sensitivity. Many of the reagents needed for the new assays are commercially available, and those that are not are being prepared under Good Manufacturing Procedures for approval by the FDA. Our newborn screening assay for Krabbe disease is currently being put in place at the Wadsworth Center in New York State for the analysis of similar to 1000 dried blood spots per day. Summary We have developed tandem mass spectrometry for the direct assay of lysosomal enzymes in rehydrated dried blood spots that can be implemented for newborn screening of lysosomal storage disorders. Several enzymes can be analysed by a single method (multiplex analysis) and in a high-throughput manner appropriate for newborn screening laboratories.
引用
收藏
页码:397 / 404
页数:8
相关论文
共 50 条
  • [21] Tandem mass spectrometry analysis of dried urine spots for newborn screening of mucopolysaccharidoses
    Auray-Blais, Christiane
    Menkovic, Iskren
    Boutin, Michel
    Lavoie, Pamela
    MOLECULAR GENETICS AND METABOLISM, 2023, 138 (02) : 11 - 12
  • [22] Establishment of Cutoff Values for Newborn Screening of Six Lysosomal Storage Disorders by Tandem Mass Spectrometry
    Li, Ruotong
    Tian, Liping
    Gao, Qing
    Guo, Yuanfang
    Li, Gaijie
    Li, Yulin
    Sun, Meng
    Yan, Yan
    Li, Qing
    Nie, Wenying
    Zou, Hui
    FRONTIERS IN PEDIATRICS, 2022, 10
  • [23] Use of Tandem Mass Spectrometry for Newborn Screening of 6 Lysosomal Storage Disorders in a Korean Population
    Han, Minje
    Jun, Sun-Hee
    Song, Sang Hoon
    Park, Kyoung Un
    Kim, Jin Q.
    Song, Junghan
    KOREAN JOURNAL OF LABORATORY MEDICINE, 2011, 31 (04): : 250 - 256
  • [24] Lysosomal storage disorder 4+1 multiplex assay for newborn screening using tandem mass spectrometry: Application to a small-scale population study for five lysosomal storage disorders
    Orsini, Joseph J.
    Martin, Monica M.
    Showers, Amanda L.
    Bodamer, Olaf A.
    Zhang, X. Kate
    Gelb, Michael H.
    Caggana, Michele
    CLINICA CHIMICA ACTA, 2012, 413 (15-16) : 1270 - 1273
  • [25] Incorporating the measurement of EDTA in dried blood spots (DBS) by tandem mass spectrometry in routine newborn screening
    Fisher, Lawrence J.
    Al-Dirbashi, Osama Y.
    Ogrel, Svetlana
    McIntosh, Nathan
    Geraghty, Michael T.
    Chakraborty, Pranesh
    CLINICAL BIOCHEMISTRY, 2014, 47 (15) : 144 - 144
  • [26] Changes in Solvent Composition in Tandem Mass Spectrometry Multiplex Assay for Lysosomal Storage Disorders Do Not Affect Assay Results
    De Jesus, Victor R.
    Zhou, Hui
    Vogt, Robert F.
    Hannon, W. Harry
    CLINICAL CHEMISTRY, 2009, 55 (03) : 596 - 598
  • [27] A new multiplex analysis of glucosylsphingosine and globotriaosylsphingosine in dried blood spots by tandem mass spectrometry
    Van Baelen, Amber
    Roosens, Laurence
    Devos, Sylvie
    Verhulst, Stijn
    Eyskens, Francois
    MOLECULAR GENETICS AND METABOLISM REPORTS, 2023, 37
  • [28] Dried blood spots in the diagnosis of lysosomal storage disorders-Possibilities for newborn screening and high-risk population screening
    Lukacs, Z.
    Cobos, P. Nieves
    Keil, A.
    Hartung, R.
    Mengel, E.
    Beck, M.
    Deschauer, M.
    Hanisch, F.
    Santer, R.
    CLINICAL BIOCHEMISTRY, 2011, 44 (07) : 476 - 476
  • [29] Identification of inherited disorders by tandem mass spectrometry analysis of dried blood spots
    Chernonosov, A.
    Alekseeva, I.
    Fedorova, O.
    FEBS JOURNAL, 2013, 280 : 278 - 278
  • [30] Newborn screening for hepatorenal tyrosinemia by tandem mass spectrometry: analysis of succinylacetone extracted from dried blood spots
    Allard, P
    Grenier, A
    Korson, MS
    Zytkovicz, TH
    CLINICAL BIOCHEMISTRY, 2004, 37 (11) : 1010 - 1015