AN AUTOMATED ENZYMATIC METHOD ON THE ROCHE COBAS MIRA(TM)-S FOR MONITORING PHENYLALANINE IN DRIED BLOOD SPOTS OF PATIENTS WITH PHENYLKETONURIA

Citation
Ew. Randell et Dc. Lehotay, AN AUTOMATED ENZYMATIC METHOD ON THE ROCHE COBAS MIRA(TM)-S FOR MONITORING PHENYLALANINE IN DRIED BLOOD SPOTS OF PATIENTS WITH PHENYLKETONURIA, Clinical biochemistry, 29(2), 1996, pp. 133-138
Citations number
26
Categorie Soggetti
Biology,"Chemistry Medicinal
Journal title
ISSN journal
00099120
Volume
29
Issue
2
Year of publication
1996
Pages
133 - 138
Database
ISI
SICI code
0009-9120(1996)29:2<133:AAEMOT>2.0.ZU;2-L
Abstract
Objective: To describe and evaluate a phenylalanine dehydrogenase-coup led enzymatic assay for blood-spot phenylalanine (Phe) automated on th e COBAs MIRA(TM) S analyzer for monitoring Phe in phenylketonuria (PKU ) patients, as part of a home testing program. Methods and Results: Th is method required a four-point calibration with each run and the usef ul range was 9.3 to 3500 mu mol/L Phe. The within-run precision (CV%) was 8.8% at a mean of 77 mu mol/L Phe and 5.3% at 787 mu mol/L Phe. Th e between-run precision was 15% and 5.6% for 104 mu mol/L and 748 umol /L Phe, respectively. Blood-spot Phe determinations by this method wer e compared with plasma Phe determined by the Beckman System 7300 HPLC analyzer using 152 samples collected from PKU patients and 56 samples from patients without PKU. Linear regression analysis revealed the equ ation y = 0.933x + 14.9. The standard error of estimate (Sy.x) was 82. 9 and the correlation coefficient (r) was 0.98. A positive bias, obser ved for the blood-spot Phe assay with specimens containing Phe concent rations below 200 mu mol/L, was not due to carryover or tyrosine.Concl usion: The results indicate that this method is acceptable for monitor ing blood Phe levels in PKU patients.