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Repository of intra- and inter-run variations of quantitative autoantibody assays: A European multicenter study

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Autor
Dragon-Durey M.-A., Bizzaro N., Senant M., Andreeva H., Bogdanos D.P., Bonroy C., Bossuyt X., Eriksson C., Fabien N., Heijnen I., Herold M., Musset L., Kuhi L., Lopez-Hoyos M., Berki T., Roozendaal C., Sack U., Sundic T., Taylor L., Kuna A.T., Damoiseaux J.
Fecha
2022
Language
en
DOI
10.1515/cclm-2022-0411
Materia
autoantibody
beta2 glycoprotein 1 antibody
cardiolipin antibody
cyclic citrullinated peptide antibody
double stranded DNA antibody
gliadin antibody
immunoglobulin G
immunoglobulin M
protein glutamine gamma glutamyltransferase antibody
rheumatoid factor
thyroglobulin antibody
thyrotropin receptor antibody
autoantibody
accreditation
addressable laser bead immunoassay
Article
Austria
Belgium
benchmarking
controlled study
Croatia
enzyme linked immunosorbent assay
Estonia
fluorescent enzyme immunoassay
France
Germany
Greece
human
Hungary
immunoassay
Italy
laboratory
multicenter study
nephelometry
Netherlands
Norway
quality control
quantitative assay
Spain
Sweden
Switzerland
turbidimetry
United Kingdom
clinical laboratory service
clinical trial
quality control
standard
Autoantibodies
Clinical Laboratory Services
Humans
Laboratories
Quality Control
Reference Standards
De Gruyter Open Ltd
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Resumen
Objectives: No reference data are available on repositories to measure precision of autoantibody assays. The scope of this study was to document inter- and intra-run variations of quantitative autoantibody assays based on a real-world large international data set. Methods: Members of the European Autoimmunity Standardisation Initiative (EASI) group collected the data of intra- and inter-run variability obtained with assays quantifying 15 different autoantibodies in voluntary participating laboratories from their country. We analyzed the impact on the assay performances of the type of immunoassay, the number of measurements used to calculate the coefficient of variation (CVs), the nature and the autoantibody level of the internal quality control (IQC). Results: Data were obtained from 64 laboratories from 15 European countries between February and October 2021. We analyzed 686 and 1,331 values of intra- and inter-run CVs, respectively. Both CVs were significantly dependent on: the method of immunoassay, the level of IQC with higher imprecision observed when the antibody levels were lower than 2-fold the threshold for positivity, and the nature of the IQC with commercial IQCs having lower CVs than patients-derived IQCs. Our analyses also show that the type of autoantibody has low impact on the assay' performances and that 15 measurements are sufficient to establish reliable intra- and inter-run variations. Conclusions: This study provides for the first time an international repository yielding values of intra- and inter-run variation for quantitative autoantibody assays. These data could be useful for ISO 15189 accreditation requirements and will allow clinical diagnostic laboratories to assure quality of patient results. © 2022 Walter de Gruyter GmbH, Berlin/Boston.
URI
http://hdl.handle.net/11615/73466
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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