Evaluation of the new restandardized Abbott Architect 25‐OH Vitamin D assay in vitamin D‐insufficient and vitamin D‐supplemented individuals

Background Recently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical performance of the restandardized Architect 25(OH)D assay and compared its performance with a NIST‐traceable liquid chromatography‐tandem ma...

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Published inJournal of clinical laboratory analysis Vol. 32; no. 4; pp. e22328 - n/a
Main Authors Annema, Wijtske, Nowak, Albina, Eckardstein, Arnold, Saleh, Lanja
Format Journal Article
LanguageEnglish
Published United States John Wiley & Sons, Inc 01.05.2018
John Wiley and Sons Inc
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Online AccessGet full text
ISSN0887-8013
1098-2825
1098-2825
DOI10.1002/jcla.22328

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Abstract Background Recently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical performance of the restandardized Architect 25(OH)D assay and compared its performance with a NIST‐traceable liquid chromatography‐tandem mass spectrometry (LC‐MS/MS) method and the Roche total 25(OH)D assay in vitamin D‐insufficient individuals before and after vitamin D3 supplementation. Methods Frozen serum samples were obtained from 88 healthy subjects with self‐perceived fatigue and vitamin D‐insufficiency <50 nmol L−1 who were randomized to receive a single 100 000 IU dose of vitamin D3 (n = 48) or placebo (n = 40). Total 25(OH)D concentrations were measured before and 4 weeks after supplementation by the restandardized Architect 25(OH)D assay, LC‐MS/MS, and Roche assay. Results The Architect 25(OH)D assay showed an intra‐ and inter‐assay imprecision of <5%. Comparison of the Architect assay with the LC‐MS/MS method showed a good correlation in both vitamin D‐insufficient and vitamin D‐supplemented subjects, however, with a negative mean bias of 17.4% and 8.9%, respectively. As compared to the Roche assay, the Abbott assay underestimated 25(OH)D results in insufficient subjects (<50 nmol L−1) with a mean negative bias of 17.1%, this negative bias turned into a positive bias in supplemented subjects. Overall there was a moderate agreement in classification of vitamin D‐insufficient and ‐supplemented individuals into different vitamin D states between the Architect 25(OH)D method and LC‐MS/MS. Conclusion The routine use of the restandardized Architect 25(OH)D results in a slight underestimation of circulating total 25(OH)D levels at lower concentrations and thus potential misclassification of vitamin D status.
AbstractList Recently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical performance of the restandardized Architect 25(OH)D assay and compared its performance with a NIST-traceable liquid chromatography-tandem mass spectrometry (LC-MS/MS) method and the Roche total 25(OH)D assay in vitamin D-insufficient individuals before and after vitamin D3 supplementation.BACKGROUNDRecently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical performance of the restandardized Architect 25(OH)D assay and compared its performance with a NIST-traceable liquid chromatography-tandem mass spectrometry (LC-MS/MS) method and the Roche total 25(OH)D assay in vitamin D-insufficient individuals before and after vitamin D3 supplementation.Frozen serum samples were obtained from 88 healthy subjects with self-perceived fatigue and vitamin D-insufficiency <50 nmol L-1 who were randomized to receive a single 100 000 IU dose of vitamin D3 (n = 48) or placebo (n = 40). Total 25(OH)D concentrations were measured before and 4 weeks after supplementation by the restandardized Architect 25(OH)D assay, LC-MS/MS, and Roche assay.METHODSFrozen serum samples were obtained from 88 healthy subjects with self-perceived fatigue and vitamin D-insufficiency <50 nmol L-1 who were randomized to receive a single 100 000 IU dose of vitamin D3 (n = 48) or placebo (n = 40). Total 25(OH)D concentrations were measured before and 4 weeks after supplementation by the restandardized Architect 25(OH)D assay, LC-MS/MS, and Roche assay.The Architect 25(OH)D assay showed an intra- and inter-assay imprecision of <5%. Comparison of the Architect assay with the LC-MS/MS method showed a good correlation in both vitamin D-insufficient and vitamin D-supplemented subjects, however, with a negative mean bias of 17.4% and 8.9%, respectively. As compared to the Roche assay, the Abbott assay underestimated 25(OH)D results in insufficient subjects (<50 nmol L-1 ) with a mean negative bias of 17.1%, this negative bias turned into a positive bias in supplemented subjects. Overall there was a moderate agreement in classification of vitamin D-insufficient and -supplemented individuals into different vitamin D states between the Architect 25(OH)D method and LC-MS/MS.RESULTSThe Architect 25(OH)D assay showed an intra- and inter-assay imprecision of <5%. Comparison of the Architect assay with the LC-MS/MS method showed a good correlation in both vitamin D-insufficient and vitamin D-supplemented subjects, however, with a negative mean bias of 17.4% and 8.9%, respectively. As compared to the Roche assay, the Abbott assay underestimated 25(OH)D results in insufficient subjects (<50 nmol L-1 ) with a mean negative bias of 17.1%, this negative bias turned into a positive bias in supplemented subjects. Overall there was a moderate agreement in classification of vitamin D-insufficient and -supplemented individuals into different vitamin D states between the Architect 25(OH)D method and LC-MS/MS.The routine use of the restandardized Architect 25(OH)D results in a slight underestimation of circulating total 25(OH)D levels at lower concentrations and thus potential misclassification of vitamin D status.CONCLUSIONThe routine use of the restandardized Architect 25(OH)D results in a slight underestimation of circulating total 25(OH)D levels at lower concentrations and thus potential misclassification of vitamin D status.
Recently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical performance of the restandardized Architect 25(OH)D assay and compared its performance with a NIST-traceable liquid chromatography-tandem mass spectrometry (LC-MS/MS) method and the Roche total 25(OH)D assay in vitamin D-insufficient individuals before and after vitamin D supplementation. Frozen serum samples were obtained from 88 healthy subjects with self-perceived fatigue and vitamin D-insufficiency <50 nmol L who were randomized to receive a single 100 000 IU dose of vitamin D (n = 48) or placebo (n = 40). Total 25(OH)D concentrations were measured before and 4 weeks after supplementation by the restandardized Architect 25(OH)D assay, LC-MS/MS, and Roche assay. The Architect 25(OH)D assay showed an intra- and inter-assay imprecision of <5%. Comparison of the Architect assay with the LC-MS/MS method showed a good correlation in both vitamin D-insufficient and vitamin D-supplemented subjects, however, with a negative mean bias of 17.4% and 8.9%, respectively. As compared to the Roche assay, the Abbott assay underestimated 25(OH)D results in insufficient subjects (<50 nmol L ) with a mean negative bias of 17.1%, this negative bias turned into a positive bias in supplemented subjects. Overall there was a moderate agreement in classification of vitamin D-insufficient and -supplemented individuals into different vitamin D states between the Architect 25(OH)D method and LC-MS/MS. The routine use of the restandardized Architect 25(OH)D results in a slight underestimation of circulating total 25(OH)D levels at lower concentrations and thus potential misclassification of vitamin D status.
BackgroundRecently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical performance of the restandardized Architect 25(OH)D assay and compared its performance with a NIST‐traceable liquid chromatography‐tandem mass spectrometry (LC‐MS/MS) method and the Roche total 25(OH)D assay in vitamin D‐insufficient individuals before and after vitamin D3 supplementation.MethodsFrozen serum samples were obtained from 88 healthy subjects with self‐perceived fatigue and vitamin D‐insufficiency <50 nmol L−1 who were randomized to receive a single 100 000 IU dose of vitamin D3 (n = 48) or placebo (n = 40). Total 25(OH)D concentrations were measured before and 4 weeks after supplementation by the restandardized Architect 25(OH)D assay, LC‐MS/MS, and Roche assay.ResultsThe Architect 25(OH)D assay showed an intra‐ and inter‐assay imprecision of <5%. Comparison of the Architect assay with the LC‐MS/MS method showed a good correlation in both vitamin D‐insufficient and vitamin D‐supplemented subjects, however, with a negative mean bias of 17.4% and 8.9%, respectively. As compared to the Roche assay, the Abbott assay underestimated 25(OH)D results in insufficient subjects (<50 nmol L−1) with a mean negative bias of 17.1%, this negative bias turned into a positive bias in supplemented subjects. Overall there was a moderate agreement in classification of vitamin D‐insufficient and ‐supplemented individuals into different vitamin D states between the Architect 25(OH)D method and LC‐MS/MS.ConclusionThe routine use of the restandardized Architect 25(OH)D results in a slight underestimation of circulating total 25(OH)D levels at lower concentrations and thus potential misclassification of vitamin D status.
Background Recently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical performance of the restandardized Architect 25(OH)D assay and compared its performance with a NIST‐traceable liquid chromatography‐tandem mass spectrometry (LC‐MS/MS) method and the Roche total 25(OH)D assay in vitamin D‐insufficient individuals before and after vitamin D3 supplementation. Methods Frozen serum samples were obtained from 88 healthy subjects with self‐perceived fatigue and vitamin D‐insufficiency <50 nmol L−1 who were randomized to receive a single 100 000 IU dose of vitamin D3 (n = 48) or placebo (n = 40). Total 25(OH)D concentrations were measured before and 4 weeks after supplementation by the restandardized Architect 25(OH)D assay, LC‐MS/MS, and Roche assay. Results The Architect 25(OH)D assay showed an intra‐ and inter‐assay imprecision of <5%. Comparison of the Architect assay with the LC‐MS/MS method showed a good correlation in both vitamin D‐insufficient and vitamin D‐supplemented subjects, however, with a negative mean bias of 17.4% and 8.9%, respectively. As compared to the Roche assay, the Abbott assay underestimated 25(OH)D results in insufficient subjects (<50 nmol L−1) with a mean negative bias of 17.1%, this negative bias turned into a positive bias in supplemented subjects. Overall there was a moderate agreement in classification of vitamin D‐insufficient and ‐supplemented individuals into different vitamin D states between the Architect 25(OH)D method and LC‐MS/MS. Conclusion The routine use of the restandardized Architect 25(OH)D results in a slight underestimation of circulating total 25(OH)D levels at lower concentrations and thus potential misclassification of vitamin D status.
Author Eckardstein, Arnold
Saleh, Lanja
Annema, Wijtske
Nowak, Albina
AuthorAffiliation 1 Institute of Clinical Chemistry University Hospital of Zurich and University of Zurich Zurich Switzerland
2 Division of Internal Medicine University Hospital of Zurich and University of Zurich Zurich Switzerland
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Issue 4
Keywords vitamin D assays
immunoassays
25-hydroxy vitamin D
liquid chromatography-tandem mass spectrometry (LC-MS/MS)
Language English
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  article-title: Analytical and clinical evaluation of the new Fujirebio Lumipulse(R)G non‐competitive assay for 25(OH)‐vitamin D and three immunoassays for 25(OH)D in healthy subjects, osteoporotic patients, third trimester pregnant women, healthy African subjects, hemodialyzed and intensive care patients
  publication-title: Clin Chem Lab Med
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  doi: 10.1515/cclm-2016-1129
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Snippet Background Recently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical...
Recently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical...
BackgroundRecently, Abbott Diagnostics has restandardized the Architect 25(OH)D assay against the NIST SRM 2972. We have evaluated the analytical and clinical...
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StartPage e22328
SubjectTerms 25‐hydroxy vitamin D
Architects
Bias
Fatigue
immunoassays
Liquid chromatography
liquid chromatography‐tandem mass spectrometry (LC‐MS/MS)
Mass spectroscopy
Supplements
Vitamin D
vitamin D assays
Vitamin D3
Title Evaluation of the new restandardized Abbott Architect 25‐OH Vitamin D assay in vitamin D‐insufficient and vitamin D‐supplemented individuals
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjcla.22328
https://www.ncbi.nlm.nih.gov/pubmed/28926129
https://www.proquest.com/docview/2047322588
https://www.proquest.com/docview/1940597857
https://pubmed.ncbi.nlm.nih.gov/PMC6817053
Volume 32
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