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

Abstract

BACKGROUND:

Deficiency of the lysosomal enzyme galactosylcerebrosidase (GALC) causes Krabbe disease. Newborn screening for Krabbe disease is ongoing, but improved methods for follow-up analysis of screen-positive babies are needed to better advise families and to optimize treatment. We report a new assay for the enzymatic activity of GALC in lymphocytes.

METHODS:

T lymphocytes were isolated from venous blood by magnetic bead technology. The assay used a close structural analog of the natural substrate and LC-MS/MS to quantify the amount of product with the aid of a chemically identical internal standard.

RESULTS:

The analytical range of the assay (ratio of assay response for the QC high standard to that from all non-enzymatic-dependent processes) was 20-fold greater than that for the conventional radiometric GALC assay. The LC-MS/MS could distinguish cells that were null in GALC from those that contained traces of active enzyme (down to 0.3% of normal). There was a good correlation between the level of residual GALC activity in lymphocytes and the severity of Krabbe disease.

CONCLUSIONS:

The new assay can measure small amounts of residual GALC activity in leukocytes with high accuracy compared to previous assays and can contribute, along with genotyping, biomarker analysis, and neurological imaging, a better plan for post-newborn screening follow-up for 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
• Journal: Clinical chemistry (Clin Chem) Vol. 63 Issue 8 Pg. 1363-1369 (Aug 2017) ISSN: 1530-8561 [Electronic] England
• PMID: 28592445 (Publication Type: Journal Article)
• Copyright: © 2017 American Association for Clinical Chemistry.

Chemical References

• Galactosylceramidase

Topics

• Child
• Chromatography, Liquid
• Galactosylceramidase (analysis, deficiency, metabolism)
• Humans
• Infant, Newborn
• Leukodystrophy, Globoid Cell (enzymology, metabolism)
• Neonatal Screening (methods)
• T-Lymphocytes (enzymology, metabolism)
• Tandem Mass Spectrometry