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


Journal

RMD open
ISSN: 2056-5933
Titre abrégé: RMD Open
Pays: England
ID NLM: 101662038

Informations de publication

Date de publication:
03 2022
Historique:
received: 13 11 2021
accepted: 21 02 2022
entrez: 24 3 2022
pubmed: 25 3 2022
medline: 7 4 2022
Statut: ppublish

Résumé

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. 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. 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. Defining thresholds for antibody levels and assigning test result interval-specific LRs allows alignment of clinical interpretation for all RF and ACPA assays.

Sections du résumé

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.

Identifiants

pubmed: 35321875
pii: rmdopen-2021-002099
doi: 10.1136/rmdopen-2021-002099
pmc: PMC8943733
pii:
doi:

Substances chimiques

Anti-Citrullinated Protein Antibodies 0
Peptides 0
Rheumatoid Factor 9009-79-4

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 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.

Déclaration de conflit d'intérêts

Competing interests: XB, LVH, GS and DS have received speaker fees from and have been a consultant for Thermo Fisher Scientific. LBernasconi and IH have received speaker fees from Thermo Fisher Scientific. DA and PJ are editorial board members of RMD Open. All participating diagnostic companies in-kind supported with RF/ACPA assays and technical training: Thermo Fisher Scientific, Uppsala, Sweden; Cambridge Life Science, Ely, UK; Ortho-Clinical Diagnostics, Raritan, New Jersey, USA; Diagam, Ghislenghien, Belgium; Roche Diagnostics, Mannheim, Germany; Svar Life Science, Malmö, Sweden; Immunodiagnostic Systems, Tyne and Wear, UK; Orgentec, Mainz, Germany; Abbott, Wiesbaden, Germany; Euroimmun, Lübeck, Germany; Bio-Rad Laboratories, Hercules, California, USA; and Siemens Healthineers, Sudbury, UK.

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Auteurs

Lieve Van Hoovels (L)

Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium Lieve.Van.Hoovels@olvz-aalst.be.
Department of Laboratory Medicine, OLV Ziekenhuis, Aalst, Belgium.

Bert Vander Cruyssen (B)

Department of Rheumatology, OLV Ziekenhuis, Aalst, Belgium.

Daniela Sieghart (D)

Division of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.

Carolien Bonroy (C)

Department of Internal Medicine, Ghent University, Ghent, Belgium.
Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.

Eszter Nagy (E)

Department of Laboratory Medicine, National Institute of Locomotor Diseases and Disabilities, Budapest, Hungary.

Rille Pullerits (R)

Department of Clinical Immunology and Transfusion Medicine, Sahlgrenska University Hospital, Gotheburg, Sweden.
Department of Rheumatology, Sahlgrenska Academy, Gothenburg, Sweden.

Saša Čučnik (S)

Department of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.

Charlotte Dahle (C)

Division of Inflammation and Infection, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.

Ingmar Heijnen (I)

Department of Laboratory Medicine, University Hospital Basel, Basel, Switzerland.

Luca Bernasconi (L)

Department of Laboratory Medicine, Kantonsspital Aarau AG, Aarau, Switzerland.

Farid Benkhadra (F)

Department of Laboratory Medicine, Centre Hospitalier de Luxembourg, Luxembourg, Luxembourg.

Laura Bogaert (L)

Department of Laboratory Medicine, OLV Ziekenhuis, Aalst, Belgium.

Stefanie Van Den Bremt (S)

Department of Laboratory Medicine, OLV Ziekenhuis, Aalst, Belgium.

Ann Van Liedekerke (A)

Department of Laboratory Medicine, AZ Sint-Elisabeth Ziekenhuis Zottegem, Zottegem, Belgium.

Geert Vanheule (G)

Department of Laboratory Medicine, AZ Rivierenland Campus Bornem, Bornem, Belgium.

Johan Robbrecht (J)

Department of Laboratory Medicine, AZ Sint-Lucas Brugge, Brugge, Belgium.

Lucy Studholme (L)

National Institute for Biological Standards and Control, Hertfordshire, UK.

Claudine Wirth (C)

Department of Rheumatology, Centre Hospitalier de Luxembourg, Luxembourg, Luxembourg.

Rüdiger Müller (R)

Department of Rheumatology, Rheumazentrum Ostschweiz, St. Gallen, Switzerland.

Diego Kyburz (D)

Department of Rheumatology, University Hospital Basel, Basel, Switzerland.

Christopher Sjöwall (C)

Division of Inflammation and Infection, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.

Alf Kastbom (A)

Division of Inflammation and Infection, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.

Rok Ješe (R)

Department of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.

Boja Jovancevic (B)

Department of Rheumatology, Sahlgrenska Academy, Gothenburg, Sweden.

Emese Kiss (E)

Department of Clinical Immunology, Adult and Pediatric Rheumatology, National Institute of Locomotor Diseases and Disabilities, Budapest, Hungary.

Peggy Jacques (P)

Department of Rheumatology, University Hospital Ghent and VIB Inflammation Research Center, Ghent, Belgium.

Daniel Aletaha (D)

Division of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.

Guenter Steiner (G)

Division of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
Ludwig Boltzmann Institute for Arthritis and Rehabilitation, Vienna, Austria.

Patrick Verschueren (P)

Department of Rheumatology, KU Leuven University Hospitals Leuven, Leuven, Belgium.
Department of Development and Regeneration, Skeletal Biology and Engineering Research Centre, KU Leuven Biomedical Sciences Group, Leuven, Belgium.

Xavier Bossuyt (X)

Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Department of Laboratory Medicine, KU Leuven University Hospitals Leuven, Leuven, Belgium.

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