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Automated Competitive Protein‐Binding Assay for Total 25‐OH Vitamin D, Multicenter Evaluation and Practical Performance
BACKGROUND: The Roche Elecsys Vitamin D Total competitive protein‐binding assay uses recombinant vitamin D binding protein for measuring 25‐hydroxyvitamin D (25‐OHD), which is different from commonly used antibody assays. METHODS: The assay, standardized against LC‐MS/MS, was tested at four sites. E...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6807057/ https://www.ncbi.nlm.nih.gov/pubmed/25132191 http://dx.doi.org/10.1002/jcla.21793 |
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author | Wielders, Jos PM Carter, Graeme F. Eberl, Heike Morris, Gary Jürgen Roth, Heinz Vogl, Christian |
author_facet | Wielders, Jos PM Carter, Graeme F. Eberl, Heike Morris, Gary Jürgen Roth, Heinz Vogl, Christian |
author_sort | Wielders, Jos PM |
collection | PubMed |
description | BACKGROUND: The Roche Elecsys Vitamin D Total competitive protein‐binding assay uses recombinant vitamin D binding protein for measuring 25‐hydroxyvitamin D (25‐OHD), which is different from commonly used antibody assays. METHODS: The assay, standardized against LC‐MS/MS, was tested at four sites. Evaluation included precision; between‐laboratory variability; functional sensitivity; correlation to LC‐MS/MS, HPLC, and immunoassays; as well as robustness, traceability, and EQAS performance. RESULTS: Precision testing showed within‐run coefficient of variations (CVs) of ≤7%, within‐laboratory CVs of <9.5%, between‐laboratory precision CVs of ≤10.1%, and a functional sensitivity below 9.8 nmol/l (at CV 12.9%). The assay showed equivalent 25‐OHD levels for matched serum and plasma samples, good reagent lot‐to‐lot consistency in pooled sera over time, and good agreement with HPLC (relative bias −8.8%). Comparison with LC‐MS/MS methods yielded relative biases of −15.4, −13.5, −10.2, and 3.2%. Comparison against immunoassays showed a relative bias of 14.5% (DiaSorin Liaison) and −58.2% (IDS‐iSYS). The overall mean results in 2 years DEQAS was 102% of the ALTM. In a certified reference patient panel, the average bias was <4% for the sum of 25‐OHD2 and 25‐OHD3. CONCLUSION: The Elecsys Vitamin D Total assay demonstrated good overall performance and is, according to present standards, very suitable for automated measurement of 25‐OHD. |
format | Online Article Text |
id | pubmed-6807057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68070572019-11-12 Automated Competitive Protein‐Binding Assay for Total 25‐OH Vitamin D, Multicenter Evaluation and Practical Performance Wielders, Jos PM Carter, Graeme F. Eberl, Heike Morris, Gary Jürgen Roth, Heinz Vogl, Christian J Clin Lab Anal Original Articles BACKGROUND: The Roche Elecsys Vitamin D Total competitive protein‐binding assay uses recombinant vitamin D binding protein for measuring 25‐hydroxyvitamin D (25‐OHD), which is different from commonly used antibody assays. METHODS: The assay, standardized against LC‐MS/MS, was tested at four sites. Evaluation included precision; between‐laboratory variability; functional sensitivity; correlation to LC‐MS/MS, HPLC, and immunoassays; as well as robustness, traceability, and EQAS performance. RESULTS: Precision testing showed within‐run coefficient of variations (CVs) of ≤7%, within‐laboratory CVs of <9.5%, between‐laboratory precision CVs of ≤10.1%, and a functional sensitivity below 9.8 nmol/l (at CV 12.9%). The assay showed equivalent 25‐OHD levels for matched serum and plasma samples, good reagent lot‐to‐lot consistency in pooled sera over time, and good agreement with HPLC (relative bias −8.8%). Comparison with LC‐MS/MS methods yielded relative biases of −15.4, −13.5, −10.2, and 3.2%. Comparison against immunoassays showed a relative bias of 14.5% (DiaSorin Liaison) and −58.2% (IDS‐iSYS). The overall mean results in 2 years DEQAS was 102% of the ALTM. In a certified reference patient panel, the average bias was <4% for the sum of 25‐OHD2 and 25‐OHD3. CONCLUSION: The Elecsys Vitamin D Total assay demonstrated good overall performance and is, according to present standards, very suitable for automated measurement of 25‐OHD. John Wiley and Sons Inc. 2014-08-17 /pmc/articles/PMC6807057/ /pubmed/25132191 http://dx.doi.org/10.1002/jcla.21793 Text en © 2014 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Wielders, Jos PM Carter, Graeme F. Eberl, Heike Morris, Gary Jürgen Roth, Heinz Vogl, Christian Automated Competitive Protein‐Binding Assay for Total 25‐OH Vitamin D, Multicenter Evaluation and Practical Performance |
title | Automated Competitive Protein‐Binding Assay for Total 25‐OH Vitamin D, Multicenter Evaluation and Practical Performance |
title_full | Automated Competitive Protein‐Binding Assay for Total 25‐OH Vitamin D, Multicenter Evaluation and Practical Performance |
title_fullStr | Automated Competitive Protein‐Binding Assay for Total 25‐OH Vitamin D, Multicenter Evaluation and Practical Performance |
title_full_unstemmed | Automated Competitive Protein‐Binding Assay for Total 25‐OH Vitamin D, Multicenter Evaluation and Practical Performance |
title_short | Automated Competitive Protein‐Binding Assay for Total 25‐OH Vitamin D, Multicenter Evaluation and Practical Performance |
title_sort | automated competitive protein‐binding assay for total 25‐oh vitamin d, multicenter evaluation and practical performance |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6807057/ https://www.ncbi.nlm.nih.gov/pubmed/25132191 http://dx.doi.org/10.1002/jcla.21793 |
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