Literature DB >> 25762404

Measurement of psychosine in dried blood spots--a possible improvement to newborn screening programs for Krabbe disease.

Coleman T Turgeon1, Joseph J Orsini, Karen A Sanders, Mark J Magera, Thomas J Langan, Maria L Escolar, Patricia Duffner, Devin Oglesbee, Dimitar Gavrilov, Silvia Tortorelli, Piero Rinaldo, Kimiyo Raymond, Dietrich Matern.   

Abstract

BACKGROUND: Newborn screening (NBS) for Krabbe disease (KD) in New York and Missouri is conducted by measuring galactocerebrosidase (GALC) activity using tandem mass spectrometry (MS/MS). These NBS efforts have shown that the incidence of KD is unexpectedly low (1:400,000) while many individuals (ca. 1:6000) with reduced GALC activity and genotypes of uncertain significance are detected and subjected to follow up testing. Psychosine (PSY) is a putative marker of KD progression and can be measured in dried blood spots (DBS). We sought to determine the role that PSY levels play in NBS for KD, follow up, and treatment monitoring.
METHODS: PSY was eluted from DBS with methanol containing N,N-dimethyl-D-erythro-sphingosine as internal standard (IS). Liquid chromatography-MS/MS was conducted over 17 minutes in the multiple reaction monitoring positive mode to follow the precursor to product species transitions for PSY and IS. Separation of the structural isomers PSY and glucosylsphingosine was accomplished by hydrophilic interaction liquid chromatography.
RESULTS: Pre-analytical and analytical factors were studied and revealed satisfactory results. PSY was also measured in DBS collected from controls (range: <8 nmol/L, N = 220), KD patients at various disease stages (range: 8-112, N = 26), and GALC mutation carriers (range: <15 nmol/L, N = 18).
CONCLUSIONS: PSY measurement in DBS could serve as a 2nd tier assay in NBS for KD, simplify and reduce the cost of follow up protocols, help determine disease progression, and be used to monitor KD patients following hematopoietic stem cell transplantation. However, additional chronological measurements of PSY in KD patients are required to confirm these possibilities.

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Year:  2015        PMID: 25762404     DOI: 10.1007/s10545-015-9822-z

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  15 in total

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2.  Implementation of newborn screening for Krabbe disease: population study and cutoff determination.

Authors:  Joseph J Orsini; Mark A Morrissey; Laura N Slavin; Matthew Wojcik; Chad Biski; Monica Martin; Joan Keutzer; X Kate Zhang; Wei-Lien Chuang; Carole Elbin; Michele Caggana
Journal:  Clin Biochem       Date:  2009-02-09       Impact factor: 3.281

3.  Newborn screening for Krabbe disease: the New York State model.

Authors:  Patricia K Duffner; Michele Caggana; Joseph J Orsini; David A Wenger; Marc C Patterson; Carl J Crosley; Joanne Kurtzberg; Georgianne L Arnold; Maria L Escolar; Darius J Adams; Mary R Andriola; Alan M Aron; Emma Ciafaloni; Alexandra Djukic; Richard W Erbe; Patricia Galvin-Parton; Laura E Helton; Edwin H Kolodny; Barry E Kosofsky; David F Kronn; Jennifer M Kwon; Paul A Levy; Jill Miller-Horn; Thomas P Naidich; Joan E Pellegrino; James M Provenzale; Stanley J Rothman; Melissa P Wasserstein
Journal:  Pediatr Neurol       Date:  2009-04       Impact factor: 3.372

4.  Detection of the neurotoxin psychosine in samples of peripheral blood: application in diagnostics and follow-up of Krabbe disease.

Authors:  Hongling Zhu; Aurora Lopez-Rosas; Xi Qiu; Richard B Van Breemen; Ernesto R Bongarzone
Journal:  Arch Pathol Lab Med       Date:  2012-07       Impact factor: 5.534

5.  Globoid cell leukodystrophy: deficiency of lactosyl ceramide beta-galactosidase.

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6.  Psychosine, the cytotoxic sphingolipid that accumulates in globoid cell leukodystrophy, alters membrane architecture.

Authors:  Jacqueline A Hawkins-Salsbury; Archana R Parameswar; Xuntian Jiang; Paul H Schlesinger; Ernesto Bongarzone; Daniel S Ory; Alexei V Demchenko; Mark S Sands
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7.  Progressive accumulation of toxic metabolite in a genetic leukodystrophy.

Authors:  H Igisu; K Suzuki
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8.  The sphingolipid psychosine inhibits fast axonal transport in Krabbe disease by activation of GSK3β and deregulation of molecular motors.

Authors:  Ludovico Cantuti Castelvetri; Maria I Givogri; Amy Hebert; Benjamin Smith; Yuyu Song; Agnieszka Kaminska; Aurora Lopez-Rosas; Gerardo Morfini; Gustavo Pigino; Mark Sands; Scott T Brady; Ernesto R Bongarzone
Journal:  J Neurosci       Date:  2013-06-12       Impact factor: 6.167

9.  Globoid cell leukodystrophy: additional deficiency of psychosine galactosidase.

Authors:  T Miyatake; K Suzuki
Journal:  Biochem Biophys Res Commun       Date:  1972-08-07       Impact factor: 3.575

10.  Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007).

Authors:  D Matern; S Tortorelli; D Oglesbee; D Gavrilov; P Rinaldo
Journal:  J Inherit Metab Dis       Date:  2007-07-23       Impact factor: 4.982

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  24 in total

Review 1.  Newborn screening for Krabbe's disease.

Authors:  Joseph J Orsini; Carlos A Saavedra-Matiz; Michael H Gelb; Michele Caggana
Journal:  J Neurosci Res       Date:  2016-11       Impact factor: 4.164

2.  Metabolic profiling reveals biochemical pathways and potential biomarkers associated with the pathogenesis of Krabbe disease.

Authors:  Nadav I Weinstock; Lawrence Wrabetz; M Laura Feltri; Daesung Shin
Journal:  J Neurosci Res       Date:  2016-11       Impact factor: 4.164

3.  Evidence for improved survival in postsymptomatic stem cell-transplanted patients with Krabbe's disease.

Authors:  Thomas J Langan; Amy L Barcykowski; Jonathan Dare; Erin C Pannullo; Leah Muscarella; Randy L Carter
Journal:  J Neurosci Res       Date:  2016-11       Impact factor: 4.164

4.  Lymphocyte Galactocerebrosidase Activity by LC-MS/MS for Post-Newborn Screening Evaluation of Krabbe Disease.

Authors:  Hsuan-Chieh Liao; Zdenek Spacil; Farideh Ghomashchi; Maria L Escolar; Joanne Kurtzberg; Joseph J Orsini; Frantisek Turecek; C Ronald Scott; Michael H Gelb
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Review 5.  Emptying the stores: lysosomal diseases and therapeutic strategies.

Authors:  Frances M Platt
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6.  A HILIC-MS/MS method for simultaneous quantification of the lysosomal disease markers galactosylsphingosine and glucosylsphingosine in mouse serum.

Authors:  Rohini Sidhu; Christina R Mikulka; Hideji Fujiwara; Mark S Sands; Jean E Schaffer; Daniel S Ory; Xuntian Jiang
Journal:  Biomed Chromatogr       Date:  2018-04-26       Impact factor: 1.902

7.  Absolute Amounts of Analytes: When Gravimetric Methods Are Insufficient.

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Journal:  Clin Chem       Date:  2018-07-27       Impact factor: 8.327

8.  Psychosine, a marker of Krabbe phenotype and treatment effect.

Authors:  M L Escolar; B T Kiely; E Shawgo; X Hong; M H Gelb; J J Orsini; D Matern; M D Poe
Journal:  Mol Genet Metab       Date:  2017-05-22       Impact factor: 4.797

Review 9.  Contribution of tandem mass spectrometry to the diagnosis of lysosomal storage disorders.

Authors:  Monique Piraud; Magali Pettazzoni; Pamela Lavoie; Séverine Ruet; Cécile Pagan; David Cheillan; Philippe Latour; Christine Vianey-Saban; Christiane Auray-Blais; Roseline Froissart
Journal:  J Inherit Metab Dis       Date:  2018-03-19       Impact factor: 4.982

10.  Sulfatide Analysis by Mass Spectrometry for Screening of Metachromatic Leukodystrophy in Dried Blood and Urine Samples.

Authors:  Zdenek Spacil; Arun Babu Kumar; Hsuan-Chieh Liao; Christiane Auray-Blais; Samantha Stark; Teryn R Suhr; C Ronald Scott; Frantisek Turecek; Michael H Gelb
Journal:  Clin Chem       Date:  2015-11-19       Impact factor: 8.327

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