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An LC–MS/MS-Based Method for the Quantification of Pyridox(am)ine 5′-Phosphate Oxidase Activity in Dried Blood Spots from Patients with Epilepsy
Author(s) -
Matthew P. Wilson,
Emma Footitt,
Apostolos Papandreou,
MariLiis Uudelepp,
Ronit Pressler,
Danielle C. Stevenson,
Camila Pires Cremasco Gabriel,
Mel McSweeney,
Matthew Baggot,
Derek Burke,
Tommy Stödberg,
Kate Riney,
Manuel Schiff,
Simon Heales,
Kevin Mills,
Paul Gissen,
Peter T. Clayton,
Philippa B. Mills
Publication year - 2017
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.7b01358
Subject(s) - chemistry , pyridoxine , dried blood spot , dried blood , epilepsy , newborn screening , pyridoxal phosphate , gastroenterology , medicine , enzyme , chromatography , biochemistry , cofactor , psychiatry
We report the development of a rapid, simple, and robust LC-MS/MS-based enzyme assay using dried blood spots (DBS) for the diagnosis of pyridox(am)ine 5'-phosphate oxidase (PNPO) deficiency (OMIM 610090). PNPO deficiency leads to potentially fatal early infantile epileptic encephalopathy, severe developmental delay, and other features of neurological dysfunction. However, upon prompt treatment with high doses of vitamin B 6 , affected patients can have a normal developmental outcome. Prognosis of these patients is therefore reliant upon a rapid diagnosis. PNPO activity was quantified by measuring pyridoxal 5'-phosphate (PLP) concentrations in a DBS before and after a 30 min incubation with pyridoxine 5'-phosphate (PNP). Samples from 18 PNPO deficient patients (1 day-25 years), 13 children with other seizure disorders receiving B 6 supplementation (1 month-16 years), and 37 child hospital controls (5 days-15 years) were analyzed. DBS from the PNPO-deficient samples showed enzyme activity levels lower than all samples from these two other groups as well as seven adult controls; no false positives or negatives were identified. The method was fully validated and is suitable for translation into the clinical diagnostic arena.

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