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Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results

BACKGROUND: Rheumatoid factor (RF) and anti-citrullinated protein/peptide antibodies (ACPA) are important biomarkers for diagnosis of rheumatoid arthritis (RA). However, there is poor harmonisation of RF and ACPA assays. The aim of this study was to refine RF and ACPA interpretation across commercia...

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Autores principales: Van Hoovels, Lieve, Vander Cruyssen, Bert, Sieghart, Daniela, Bonroy, Carolien, Nagy, Eszter, Pullerits, Rille, Čučnik, Saša, Dahle, Charlotte, Heijnen, Ingmar, Bernasconi, Luca, Benkhadra, Farid, Bogaert, Laura, Van Den Bremt, Stefanie, Van Liedekerke, Ann, Vanheule, Geert, Robbrecht, Johan, Studholme, Lucy, Wirth, Claudine, Müller, Rüdiger, Kyburz, Diego, Sjöwall, Christopher, Kastbom, Alf, Ješe, Rok, Jovancevic, Boja, Kiss, Emese, Jacques, Peggy, Aletaha, Daniel, Steiner, Guenter, Verschueren, Patrick, Bossuyt, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943733/
https://www.ncbi.nlm.nih.gov/pubmed/35321875
http://dx.doi.org/10.1136/rmdopen-2021-002099
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author Van Hoovels, Lieve
Vander Cruyssen, Bert
Sieghart, Daniela
Bonroy, Carolien
Nagy, Eszter
Pullerits, Rille
Čučnik, Saša
Dahle, Charlotte
Heijnen, Ingmar
Bernasconi, Luca
Benkhadra, Farid
Bogaert, Laura
Van Den Bremt, Stefanie
Van Liedekerke, Ann
Vanheule, Geert
Robbrecht, Johan
Studholme, Lucy
Wirth, Claudine
Müller, Rüdiger
Kyburz, Diego
Sjöwall, Christopher
Kastbom, Alf
Ješe, Rok
Jovancevic, Boja
Kiss, Emese
Jacques, Peggy
Aletaha, Daniel
Steiner, Guenter
Verschueren, Patrick
Bossuyt, Xavier
author_facet Van Hoovels, Lieve
Vander Cruyssen, Bert
Sieghart, Daniela
Bonroy, Carolien
Nagy, Eszter
Pullerits, Rille
Čučnik, Saša
Dahle, Charlotte
Heijnen, Ingmar
Bernasconi, Luca
Benkhadra, Farid
Bogaert, Laura
Van Den Bremt, Stefanie
Van Liedekerke, Ann
Vanheule, Geert
Robbrecht, Johan
Studholme, Lucy
Wirth, Claudine
Müller, Rüdiger
Kyburz, Diego
Sjöwall, Christopher
Kastbom, Alf
Ješe, Rok
Jovancevic, Boja
Kiss, Emese
Jacques, Peggy
Aletaha, Daniel
Steiner, Guenter
Verschueren, Patrick
Bossuyt, Xavier
author_sort Van Hoovels, Lieve
collection PubMed
description BACKGROUND: Rheumatoid factor (RF) and anti-citrullinated protein/peptide antibodies (ACPA) are important biomarkers for diagnosis of rheumatoid arthritis (RA). However, there is poor harmonisation of RF and ACPA assays. The aim of this study was to refine RF and ACPA interpretation across commercial assays. MATERIALS AND METHODS: Six total RF isotype-non-specific assays, 3 RF IgM isotype-specific assays and 9 ACPA immunoglobulin G assays of 13 different companies were evaluated using 398 diagnostic samples from patients with RA and 1073 disease controls. RESULTS: Using cut-offs proposed by the manufacturer, there was a large variability in diagnostic sensitivity and specificity between assays. Thresholds of antibody levels were determined based on predefined specificities and used to define test result intervals. Test result interval-specific likelihood ratios (LRs) were concordant across the different RF and ACPA assays. For all assays, the LR for RA increased with increasing antibody level. Higher LRs were found for ACPA than for RF. ACPA levels associated with LRs >80 were found in a substantial fraction (>22%) of patients with RA. CONCLUSION: Defining thresholds for antibody levels and assigning test result interval-specific LRs allows alignment of clinical interpretation for all RF and ACPA assays.
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spelling pubmed-89437332022-04-08 Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results Van Hoovels, Lieve Vander Cruyssen, Bert Sieghart, Daniela Bonroy, Carolien Nagy, Eszter Pullerits, Rille Čučnik, Saša Dahle, Charlotte Heijnen, Ingmar Bernasconi, Luca Benkhadra, Farid Bogaert, Laura Van Den Bremt, Stefanie Van Liedekerke, Ann Vanheule, Geert Robbrecht, Johan Studholme, Lucy Wirth, Claudine Müller, Rüdiger Kyburz, Diego Sjöwall, Christopher Kastbom, Alf Ješe, Rok Jovancevic, Boja Kiss, Emese Jacques, Peggy Aletaha, Daniel Steiner, Guenter Verschueren, Patrick Bossuyt, Xavier RMD Open Rheumatoid Arthritis BACKGROUND: Rheumatoid factor (RF) and anti-citrullinated protein/peptide antibodies (ACPA) are important biomarkers for diagnosis of rheumatoid arthritis (RA). However, there is poor harmonisation of RF and ACPA assays. The aim of this study was to refine RF and ACPA interpretation across commercial assays. MATERIALS AND METHODS: Six total RF isotype-non-specific assays, 3 RF IgM isotype-specific assays and 9 ACPA immunoglobulin G assays of 13 different companies were evaluated using 398 diagnostic samples from patients with RA and 1073 disease controls. RESULTS: Using cut-offs proposed by the manufacturer, there was a large variability in diagnostic sensitivity and specificity between assays. Thresholds of antibody levels were determined based on predefined specificities and used to define test result intervals. Test result interval-specific likelihood ratios (LRs) were concordant across the different RF and ACPA assays. For all assays, the LR for RA increased with increasing antibody level. Higher LRs were found for ACPA than for RF. ACPA levels associated with LRs >80 were found in a substantial fraction (>22%) of patients with RA. CONCLUSION: Defining thresholds for antibody levels and assigning test result interval-specific LRs allows alignment of clinical interpretation for all RF and ACPA assays. BMJ Publishing Group 2022-03-23 /pmc/articles/PMC8943733/ /pubmed/35321875 http://dx.doi.org/10.1136/rmdopen-2021-002099 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Rheumatoid Arthritis
Van Hoovels, Lieve
Vander Cruyssen, Bert
Sieghart, Daniela
Bonroy, Carolien
Nagy, Eszter
Pullerits, Rille
Čučnik, Saša
Dahle, Charlotte
Heijnen, Ingmar
Bernasconi, Luca
Benkhadra, Farid
Bogaert, Laura
Van Den Bremt, Stefanie
Van Liedekerke, Ann
Vanheule, Geert
Robbrecht, Johan
Studholme, Lucy
Wirth, Claudine
Müller, Rüdiger
Kyburz, Diego
Sjöwall, Christopher
Kastbom, Alf
Ješe, Rok
Jovancevic, Boja
Kiss, Emese
Jacques, Peggy
Aletaha, Daniel
Steiner, Guenter
Verschueren, Patrick
Bossuyt, Xavier
Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results
title Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results
title_full Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results
title_fullStr Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results
title_full_unstemmed Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results
title_short Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results
title_sort multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results
topic Rheumatoid Arthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943733/
https://www.ncbi.nlm.nih.gov/pubmed/35321875
http://dx.doi.org/10.1136/rmdopen-2021-002099
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