Literature DB >> 16435191

External quality assurance programme for enzymatic analysis of lysosomal storage diseases: a pilot study.

G J G Ruijter1, M Boer, C W Weykamp, R de Vries, I van den Berg, J Janssens-Puister, K Niezen-Koning, R A Wevers, B J H M Poorthuis, O P van Diggelen.   

Abstract

Inborn errors of metabolism are rare and laboratories performing diagnostic tests in this field must participate in external quality assurance (EQA) schemes to demonstrate their competence and also to maintain sufficient experience with patient material. EQA schemes for metabolite analyses are available (ERNDIM), but corresponding EQA schemes for enzyme analyses are nonexistent. In this paper we describe a pilot study on lysosomal enzyme testing by four centres in The Netherlands. Quantitative aspects of EQA were studied by interlaboratory comparison of activities of six lysosomal enzymes in a series of buffy coat samples. Interlaboratory variance was enormous. To reduce variance caused by methodological differences, participants reported enzyme activities relative to mean normal values. Beta-D-Galactosidase activities compared well between the participating laboratories (average interlaboratory CV 13%), but for other enzymes large differences were observed, e.g. sphingomyelinase (average CV 38%). Diagnostic proficiency was tested with cultured fibroblasts. In 45 out of a total of 48 tests (12 cell lines, 4 participants) the correct diagnosis was accomplished on the basis of merely biochemical investigations, i.e. without clinical data of the patients. In a survey using blood of a late-onset Pompe disease patient, less conclusive results were obtained. A stable enzyme source was developed for easy distribution. Most lysosomal enzymes were stable upon lyophilization of leukocyte homogenates and during subsequent storage of the freeze-dried material at room temperature, in particular when cryolyoprotectant was added. Shipment of such lyophilized samples is simple and cheap and ideal for an EQA scheme. Our study shows that an EQA programme for enzymatic testing of lysosomal storage diseases is necessary to accomplish reliable diagnostic procedures for lysosomal storage diseases. We recommend that EQA for lysosomal enzymes be implemented through ERNDIM.

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Year:  2005        PMID: 16435191     DOI: 10.1007/s10545-005-0201-z

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


  31 in total

1.  Problems in the detection of fatty acid oxidation defects: experience of a quality assurance programme for qualitative urinary organic acid analysis.

Authors:  M Downing; J C Allen; J R Bonham; R G Edwards; N J Manning; S E Olpin; R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1999-05       Impact factor: 4.982

2.  Hurler-like phenotype: enzymatic diagnosis in dried blood spots on filter paper.

Authors:  N A Chamoles; M B Blanco; D Gaggioli; C Casentini
Journal:  Clin Chem       Date:  2001-12       Impact factor: 8.327

3.  Towards quality assurance in the determination of lysosomal enzymes: a two-centre study.

Authors:  Z Lukacs; A Keil; V Peters; A Kohlschütter; G F Hoffmann; M Cantz; J Kopitz
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

4.  A fluorimetric enzyme assay for the diagnosis of Morquio disease type A (MPS IV A).

Authors:  O P van Diggelen; H Zhao; W J Kleijer; H C Janse; B J Poorthuis; J van Pelt; J P Kamerling; H Galjaard
Journal:  Clin Chim Acta       Date:  1990-02-28       Impact factor: 3.786

5.  Stimulation of acid beta-galactosidase activity by chloride ions.

Authors:  M W Ho; J S O'Brien
Journal:  Clin Chim Acta       Date:  1970-11       Impact factor: 3.786

6.  Changes in the carbohydrate metabolism of mitogenically stimulated human peripheral lymphocytes. I. Stimulation by phytohaemagglutinin.

Authors:  D Roos; J A Loos
Journal:  Biochim Biophys Acta       Date:  1970-12-29

7.  A rapid fluorogenic palmitoyl-protein thioesterase assay: pre- and postnatal diagnosis of INCL.

Authors:  O P van Diggelen; J L Keulemans; B Winchester; I L Hofman; S L Vanhanen; P Santavuori; Y V Voznyi
Journal:  Mol Genet Metab       Date:  1999-04       Impact factor: 4.797

8.  Beta-mannosidosis: prenatal biochemical and morphological characteristics.

Authors:  M Z Jones; E J Rathke; K Cavanagh; L W Hancock
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

9.  A simple chromogenic assay for arylsulfatase A.

Authors:  M Lee-Vaupel; E Conzelmann
Journal:  Clin Chim Acta       Date:  1987-04-30       Impact factor: 3.786

10.  Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype.

Authors:  J L Keulemans; A J Reuser; M A Kroos; R Willemsen; M M Hermans; A M van den Ouweland; J G de Jong; R A Wevers; W O Renier; D Schindler; M J Coll; A Chabas; H Sakuraba; Y Suzuki; O P van Diggelen
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

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  1 in total

1.  Optimization of Enzyme Essays to Enhance Reliability of Activity Measurements in Leukocyte Lysates for the Diagnosis of Metachromatic Leukodystrophy and Gangliosidoses.

Authors:  Sebastian Strobel; Naomi Hesse; Vidiyaah Santhanakumaran; Samuel Groeschel; Gernot Bruchelt; Ingeborg Krägeloh-Mann; Judith Böhringer
Journal:  Cells       Date:  2020-11-28       Impact factor: 6.600

  1 in total

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