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
  • [31] A highly multiplexed biochemical assay for analytes in dried blood spots: application to newborn screening and diagnosis of lysosomal storage disorders and other inborn errors of metabolism
    Hong, Xinying
    Sadilek, Martin
    Gelb, Michael H.
    GENETICS IN MEDICINE, 2020, 22 (07) : 1262 - 1268
  • [32] Direct tandem mass spectrometry for the simultaneous assay of opioids, cocaine and metabolites in dried urine spots
    Otero-Fernandez, Mara
    Angel Cocho, Jose
    Jesus Tabernero, Maria
    Maria Bermejo, Ana
    Bermejo-Barrera, Pilar
    Moreda-Pineiro, Antonio
    ANALYTICA CHIMICA ACTA, 2013, 784 : 25 - 32
  • [33] Short-incubation mass spectrometry assay for lysosomal storage disorders in newborn and high-risk population screening
    Mechtler, Thomas P.
    Metz, Thomas F.
    Mueller, Hannes G.
    Ostermann, Katharina
    Ratschmann, Rene
    De Jesus, Victor R.
    Shushan, Bori
    Di Bussolo, Joseph M.
    Herman, Joseph L.
    Herkner, Kurt R.
    Kasper, David C.
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2012, 908 : 9 - 17
  • [34] Dried Blood Spot Quality Control Materials for Newborn Screening to Detect Lysosomal Storage Disorders
    De Jesus, Victor R.
    Zhou, Hui
    Vogt, Robert F.
    CLINICAL CHEMISTRY, 2013, 59 (08) : 1275 - 1276
  • [35] Pilot study of newborn screening for six lysosomal storage diseases using Tandem Mass Spectrometry
    Elliott, Susan
    Buroker, Norman
    Cournoyer, Jason J.
    Potier, Anna M.
    Trometer, Joseph D.
    Elbin, Carole
    Schermer, Mack J.
    Kantola, Jaana
    Boyce, Aaron
    Turecek, Frantisek
    Gelb, Michael H.
    Scott, C. Ronald
    MOLECULAR GENETICS AND METABOLISM, 2016, 118 (04) : 304 - 309
  • [36] Fast and direct quantification of adrenal steroids by tandem mass spectrometry in serum and dried blood spots
    Janzen, Nils
    Sander, Stefanie
    Terhardt, Michael
    Peter, Michael
    Sander, Johannes
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2008, 861 (01): : 117 - 122
  • [37] Development of tandem mass spectroscopy for the detection of lysosomal storage diseases from newborn blood spots.
    Scott, CR
    Gelb, MH
    Turecek, F
    Li, Y
    Ogata, Y
    Wang, D
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 453 - 453
  • [38] Direct dried blood spot assay of α-L-iduronidase by tandem mass spectrometry
    Chuang, WeiLien
    Pacheco, Joshua
    Elbin, Carole
    Cooper, Samantha
    Marashio, Carla
    Keutzer, Joan
    Zhang, Kate
    MOLECULAR GENETICS AND METABOLISM, 2009, 96 (02) : S17 - S17
  • [39] Contribution of tandem mass spectrometry to the diagnosis of lysosomal storage disorders
    Piraud, Monique
    Pettazzoni, Magali
    Lavoie, Pamela
    Ruet, Severine
    Pagan, Cecile
    Cheillan, David
    Latour, Philippe
    Vianey-Saban, Christine
    Auray-Blais, Christiane
    Froissart, Roseline
    JOURNAL OF INHERITED METABOLIC DISEASE, 2018, 41 (03) : 457 - 477
  • [40] Tandem mass spectrometric enzyme assay for simultaneous detection of Tay-Sachs and Sandhoff diseases in dried blood spots for newborn screening
    Herbst, Zackary M.
    Hold, Stephan
    Gelb, Michael H.
    Khaledi, Hamid
    MOLECULAR GENETICS AND METABOLISM, 2024, 142 (04)