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Accurate method for value assignment of carcinoembryonic antigen reference materials

BACKGROUND: In this study, we explored the commutability of reference materials (RMs) for carcinoembryonic antigen (CEA), selected the appropriate diluent matrix of the first International Reference Preparation (IRP) 73/601 of the World Health Organization (WHO 73/601) for CEA, and improved the comp...

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Autores principales: Zhang, Rui, Xu, Zhenzhen, Zhao, Rui, Fu, Wenxuan, Song, Yichuan, Wang, Qingtao, Yue, Yuhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10431395/
https://www.ncbi.nlm.nih.gov/pubmed/37395487
http://dx.doi.org/10.1002/jcla.24936
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author Zhang, Rui
Xu, Zhenzhen
Zhao, Rui
Fu, Wenxuan
Song, Yichuan
Wang, Qingtao
Yue, Yuhong
author_facet Zhang, Rui
Xu, Zhenzhen
Zhao, Rui
Fu, Wenxuan
Song, Yichuan
Wang, Qingtao
Yue, Yuhong
author_sort Zhang, Rui
collection PubMed
description BACKGROUND: In this study, we explored the commutability of reference materials (RMs) for carcinoembryonic antigen (CEA), selected the appropriate diluent matrix of the first International Reference Preparation (IRP) 73/601 of the World Health Organization (WHO 73/601) for CEA, and improved the comparability of CEA measurement results among different assay systems. METHODS: Forty serum samples were divided into five aliquots. WHO 73/601 was diluted into nine concentrations using five diluents with different components, and the candidate RMs for CEA at five concentrations (C1–C5) were prepared by the Beijing Clinical Laboratory Center (BCCL). The samples were analyzed via five automated CEA immunoassays. RESULTS: Carcinoembryonic antigen candidate RMs were commutable among all immunoassays based on the CLSI approach and among 7 of 10 assay combinations based on the IFCC approach. WHO 73/601 diluted in phosphate‐buffered saline (PBS) was commutable among all assays based on the CLSI approach and among 5 of 10 pairwise comparisons based on the IFCC approach with correction of bias at diluted concentrations, except for the lowest concentration, which had the smallest variation among systems. The median percentage biases among assays were decreased after calibration. CONCLUSION: The BCCL candidate RMs (C2–C5) for CEA were commutable among all immunoassays. WHO 73/601 RMs diluted in a PBS buffer matrix were selected as common calibrators for five immunoassays, which reduced bias, thereby effectively improving the harmonization of CEA detection; therefore, they could be used to assign values to CEA candidate RMs developed by BCCL. Our findings promote the harmonization of CEA detection in immunoassays.
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spelling pubmed-104313952023-08-17 Accurate method for value assignment of carcinoembryonic antigen reference materials Zhang, Rui Xu, Zhenzhen Zhao, Rui Fu, Wenxuan Song, Yichuan Wang, Qingtao Yue, Yuhong J Clin Lab Anal Research Articles BACKGROUND: In this study, we explored the commutability of reference materials (RMs) for carcinoembryonic antigen (CEA), selected the appropriate diluent matrix of the first International Reference Preparation (IRP) 73/601 of the World Health Organization (WHO 73/601) for CEA, and improved the comparability of CEA measurement results among different assay systems. METHODS: Forty serum samples were divided into five aliquots. WHO 73/601 was diluted into nine concentrations using five diluents with different components, and the candidate RMs for CEA at five concentrations (C1–C5) were prepared by the Beijing Clinical Laboratory Center (BCCL). The samples were analyzed via five automated CEA immunoassays. RESULTS: Carcinoembryonic antigen candidate RMs were commutable among all immunoassays based on the CLSI approach and among 7 of 10 assay combinations based on the IFCC approach. WHO 73/601 diluted in phosphate‐buffered saline (PBS) was commutable among all assays based on the CLSI approach and among 5 of 10 pairwise comparisons based on the IFCC approach with correction of bias at diluted concentrations, except for the lowest concentration, which had the smallest variation among systems. The median percentage biases among assays were decreased after calibration. CONCLUSION: The BCCL candidate RMs (C2–C5) for CEA were commutable among all immunoassays. WHO 73/601 RMs diluted in a PBS buffer matrix were selected as common calibrators for five immunoassays, which reduced bias, thereby effectively improving the harmonization of CEA detection; therefore, they could be used to assign values to CEA candidate RMs developed by BCCL. Our findings promote the harmonization of CEA detection in immunoassays. John Wiley and Sons Inc. 2023-07-03 /pmc/articles/PMC10431395/ /pubmed/37395487 http://dx.doi.org/10.1002/jcla.24936 Text en © 2023 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, 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 Research Articles
Zhang, Rui
Xu, Zhenzhen
Zhao, Rui
Fu, Wenxuan
Song, Yichuan
Wang, Qingtao
Yue, Yuhong
Accurate method for value assignment of carcinoembryonic antigen reference materials
title Accurate method for value assignment of carcinoembryonic antigen reference materials
title_full Accurate method for value assignment of carcinoembryonic antigen reference materials
title_fullStr Accurate method for value assignment of carcinoembryonic antigen reference materials
title_full_unstemmed Accurate method for value assignment of carcinoembryonic antigen reference materials
title_short Accurate method for value assignment of carcinoembryonic antigen reference materials
title_sort accurate method for value assignment of carcinoembryonic antigen reference materials
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10431395/
https://www.ncbi.nlm.nih.gov/pubmed/37395487
http://dx.doi.org/10.1002/jcla.24936
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