Triple Positivity for Anti–Citrullinated Protein Autoantibodies, Rheumatoid Factor, and Anti–Carbamylated Protein Antibodies Conferring High Specificity for Rheumatoid Arthritis Implications for Very Early Identification of At‐Risk Individuals
In rheumatoid arthritis (RA), anti-citrullinated protein antibodies (ACPAs) and rheumatoid factor (RF) are commonly used to aid in the diagnosis. Although these autoantibodies are mainly found in RA, their specificity is not optimal. It is therefore difficult to identify RA patients, especially in v...
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Published in | Arthritis & rheumatology (Hoboken, N.J.) Vol. 70; no. 11; pp. 1721 - 1731 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
01.11.2018
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Abstract | In rheumatoid arthritis (RA), anti-citrullinated protein antibodies (ACPAs) and rheumatoid factor (RF) are commonly used to aid in the diagnosis. Although these autoantibodies are mainly found in RA, their specificity is not optimal. It is therefore difficult to identify RA patients, especially in very early disease, based on the presence of ACPAs and RF alone. In addition, anti-carbamylated protein (anti-CarP) antibodies have diagnostic and prognostic value, since their presence is associated with joint damage in RA patients and also associated with the future development of RA in patients with arthralgia. Therefore, the aim of the present study was to investigate the value of combined antibody testing in relation to prediction and diagnosis of (early) RA.
A literature search resulted in identification of 12 relevant studies, consisting of RA patients, pre-RA individuals, disease controls, healthy first-degree relatives of RA patients, and healthy control subjects, in which data on RF, ACPAs, and anti-CarP antibody status were available. Using these data, random effects meta-analyses were carried out for several antibody combinations.
The individual antibodies were highly prevalent in patients with RA (34-80%) compared to the control groups, but were also present in non-RA controls (0-23%). For the classification of most subjects correctly as having RA or as a non-RA control, the combination of ACPAs and/or RF often performed well (specificity 65-100%, sensitivity 59-88%). However, triple positivity for ACPAs, RF, and anti-CarP antibodies resulted in a higher specificity for RA (98-100%), accompanied by a lower sensitivity (11-39%).
As the rheumatology field is moving toward very early identification of RA and possible screening for individuals at maximum risk of RA in populations with a low pretest probability, an autoantibody profile of triple positivity for ACPAs, RF, and anti-CarP provides interesting information that might help identify individuals at risk of developing RA. |
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AbstractList | In rheumatoid arthritis (RA), anti-citrullinated protein antibodies (ACPAs) and rheumatoid factor (RF) are commonly used to aid in the diagnosis. Although these autoantibodies are mainly found in RA, their specificity is not optimal. It is therefore difficult to identify RA patients, especially in very early disease, based on the presence of ACPAs and RF alone. In addition, anti-carbamylated protein (anti-CarP) antibodies have diagnostic and prognostic value, since their presence is associated with joint damage in RA patients and also associated with the future development of RA in patients with arthralgia. Therefore, the aim of the present study was to investigate the value of combined antibody testing in relation to prediction and diagnosis of (early) RA.OBJECTIVEIn rheumatoid arthritis (RA), anti-citrullinated protein antibodies (ACPAs) and rheumatoid factor (RF) are commonly used to aid in the diagnosis. Although these autoantibodies are mainly found in RA, their specificity is not optimal. It is therefore difficult to identify RA patients, especially in very early disease, based on the presence of ACPAs and RF alone. In addition, anti-carbamylated protein (anti-CarP) antibodies have diagnostic and prognostic value, since their presence is associated with joint damage in RA patients and also associated with the future development of RA in patients with arthralgia. Therefore, the aim of the present study was to investigate the value of combined antibody testing in relation to prediction and diagnosis of (early) RA.A literature search resulted in identification of 12 relevant studies, consisting of RA patients, pre-RA individuals, disease controls, healthy first-degree relatives of RA patients, and healthy control subjects, in which data on RF, ACPAs, and anti-CarP antibody status were available. Using these data, random effects meta-analyses were carried out for several antibody combinations.METHODSA literature search resulted in identification of 12 relevant studies, consisting of RA patients, pre-RA individuals, disease controls, healthy first-degree relatives of RA patients, and healthy control subjects, in which data on RF, ACPAs, and anti-CarP antibody status were available. Using these data, random effects meta-analyses were carried out for several antibody combinations.The individual antibodies were highly prevalent in patients with RA (34-80%) compared to the control groups, but were also present in non-RA controls (0-23%). For the classification of most subjects correctly as having RA or as a non-RA control, the combination of ACPAs and/or RF often performed well (specificity 65-100%, sensitivity 59-88%). However, triple positivity for ACPAs, RF, and anti-CarP antibodies resulted in a higher specificity for RA (98-100%), accompanied by a lower sensitivity (11-39%).RESULTSThe individual antibodies were highly prevalent in patients with RA (34-80%) compared to the control groups, but were also present in non-RA controls (0-23%). For the classification of most subjects correctly as having RA or as a non-RA control, the combination of ACPAs and/or RF often performed well (specificity 65-100%, sensitivity 59-88%). However, triple positivity for ACPAs, RF, and anti-CarP antibodies resulted in a higher specificity for RA (98-100%), accompanied by a lower sensitivity (11-39%).As the rheumatology field is moving toward very early identification of RA and possible screening for individuals at maximum risk of RA in populations with a low pretest probability, an autoantibody profile of triple positivity for ACPAs, RF, and anti-CarP provides interesting information that might help identify individuals at risk of developing RA.CONCLUSIONAs the rheumatology field is moving toward very early identification of RA and possible screening for individuals at maximum risk of RA in populations with a low pretest probability, an autoantibody profile of triple positivity for ACPAs, RF, and anti-CarP provides interesting information that might help identify individuals at risk of developing RA. OBJECTIVE : In rheumatoid arthritis(RA), the autoantibodies anti-citrullinated protein antibodies(ACPA) and rheumatoid factor(RF) are commonly used to aid RA diagnosis. Although these autoantibodies are mainly found in RA, their specificity is not optimal. It is therefore difficult to identify RA patients, especially in very early disease, based on the presence of ACPA and RF alone. Also, anti-carbamylated protein(anti-CarP) antibodies have diagnostic and prognostic value as the presence of anti-CarP antibodies associates with joint damage in RA patients and with future RA development in arthralgia patients. Therefore, we aimed to investigate the value of combined antibody testing in relation to prediction and diagnosis of (early) RA. METHODS : A literature search resulted in twelve studies, consisting of RA patients, pre-RA individuals, disease controls, healthy first-degree relatives of RA patients or healthy controls, in which data on RF, ACPA and anti-CarP antibody-status was available. Random effects meta-analyses were carried out for several antibody combinations. RESULTS : The individual antibodies are highly prevalent in RA(34%-80%) compared to the control groups, but are also present in non-RA controls(0%-23%). To classify most people correctly as RA or non-RA, the combination of ACPA and/or RF often performs well(specificity:65-100, sensitivity:59-88). However, triple positivity for ACPA, RF and anti-CarP antibodies results in a higher specificity(98-100) (accompanied by a lower sensitivity(11-39)). CONCLUSIONS : As the rheumatology field is moving towards very early identification of RA and possible screening for individuals at maximum risk in populations with a low pre-test probability, triple positivity provides interesting information on individuals at risk to develop RA. In rheumatoid arthritis (RA), anti-citrullinated protein antibodies (ACPAs) and rheumatoid factor (RF) are commonly used to aid in the diagnosis. Although these autoantibodies are mainly found in RA, their specificity is not optimal. It is therefore difficult to identify RA patients, especially in very early disease, based on the presence of ACPAs and RF alone. In addition, anti-carbamylated protein (anti-CarP) antibodies have diagnostic and prognostic value, since their presence is associated with joint damage in RA patients and also associated with the future development of RA in patients with arthralgia. Therefore, the aim of the present study was to investigate the value of combined antibody testing in relation to prediction and diagnosis of (early) RA. A literature search resulted in identification of 12 relevant studies, consisting of RA patients, pre-RA individuals, disease controls, healthy first-degree relatives of RA patients, and healthy control subjects, in which data on RF, ACPAs, and anti-CarP antibody status were available. Using these data, random effects meta-analyses were carried out for several antibody combinations. The individual antibodies were highly prevalent in patients with RA (34-80%) compared to the control groups, but were also present in non-RA controls (0-23%). For the classification of most subjects correctly as having RA or as a non-RA control, the combination of ACPAs and/or RF often performed well (specificity 65-100%, sensitivity 59-88%). However, triple positivity for ACPAs, RF, and anti-CarP antibodies resulted in a higher specificity for RA (98-100%), accompanied by a lower sensitivity (11-39%). As the rheumatology field is moving toward very early identification of RA and possible screening for individuals at maximum risk of RA in populations with a low pretest probability, an autoantibody profile of triple positivity for ACPAs, RF, and anti-CarP provides interesting information that might help identify individuals at risk of developing RA. |
Author | Holers, V. Michael Huizinga, Tom W. J. van der Helm‐van Mil, Annette H. M. Trouw, Leendert A. Böhringer, Stefan Rantapää‐Dahlqvist, Solbritt van der Woude, Diane Rigby, William F. C. Jones, Jonathan D. Toes, Rene E. M. Janssen, Koen M. J. Westra, Johanna Brink, Mikael Edison, Jess D. Deane, Kevin D. Verheul, Marije K. van Delft, Myrthe A. M. Gan, Ryan W. |
Author_xml | – sequence: 1 givenname: Marije K. surname: Verheul fullname: Verheul, Marije K. organization: Leiden University Medical Center Leiden The Netherlands – sequence: 2 givenname: Stefan surname: Böhringer fullname: Böhringer, Stefan organization: Leiden University Medical Center Leiden The Netherlands – sequence: 3 givenname: Myrthe A. M. surname: van Delft fullname: van Delft, Myrthe A. M. organization: Leiden University Medical Center Leiden The Netherlands – sequence: 4 givenname: Jonathan D. surname: Jones fullname: Jones, Jonathan D. organization: Geisel School of Medicine at Dartmouth Lebanon New Hampshire – sequence: 5 givenname: William F. C. surname: Rigby fullname: Rigby, William F. C. organization: Geisel School of Medicine at Dartmouth Lebanon New Hampshire – sequence: 6 givenname: Ryan W. surname: Gan fullname: Gan, Ryan W. organization: Colorado School of Public Health Aurora – sequence: 7 givenname: V. Michael surname: Holers fullname: Holers, V. Michael organization: University of Colorado Aurora – sequence: 8 givenname: Jess D. surname: Edison fullname: Edison, Jess D. organization: Walter Reed National Military Medical Center Bethesda Maryland – sequence: 9 givenname: Kevin D. surname: Deane fullname: Deane, Kevin D. organization: University of Colorado Aurora – sequence: 10 givenname: Koen M. J. surname: Janssen fullname: Janssen, Koen M. J. organization: University of Groningen and University Medical Center Groningen Groningen The Netherlands – sequence: 11 givenname: Johanna surname: Westra fullname: Westra, Johanna organization: University of Groningen and University Medical Center Groningen Groningen The Netherlands – sequence: 12 givenname: Mikael surname: Brink fullname: Brink, Mikael organization: Umeå University Umeå Sweden – sequence: 13 givenname: Solbritt surname: Rantapää‐Dahlqvist fullname: Rantapää‐Dahlqvist, Solbritt organization: Umeå University Umeå Sweden – sequence: 14 givenname: Tom W. J. surname: Huizinga fullname: Huizinga, Tom W. J. organization: Leiden University Medical Center Leiden The Netherlands – sequence: 15 givenname: Annette H. M. surname: van der Helm‐van Mil fullname: van der Helm‐van Mil, Annette H. M. organization: Leiden University Medical Center Leiden The Netherlands – sequence: 16 givenname: Diane surname: van der Woude fullname: van der Woude, Diane organization: Leiden University Medical Center Leiden The Netherlands – sequence: 17 givenname: Rene E. M. surname: Toes fullname: Toes, Rene E. M. organization: Leiden University Medical Center Leiden The Netherlands – sequence: 18 givenname: Leendert A. surname: Trouw fullname: Trouw, Leendert A. organization: Leiden University Medical Center Leiden The Netherlands |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29781231$$D View this record in MEDLINE/PubMed https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-150999$$DView record from Swedish Publication Index |
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Snippet | In rheumatoid arthritis (RA), anti-citrullinated protein antibodies (ACPAs) and rheumatoid factor (RF) are commonly used to aid in the diagnosis. Although... OBJECTIVE : In rheumatoid arthritis(RA), the autoantibodies anti-citrullinated protein antibodies(ACPA) and rheumatoid factor(RF) are commonly used to aid RA... |
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SubjectTerms | anti-carbamylated protein antibodies anti-citrullinated protein antibodies Anti-Citrullinated Protein Antibodies - immunology Arthritis, Rheumatoid - diagnosis Arthritis, Rheumatoid - immunology autoantibodies Autoantibodies - immunology Early Diagnosis Humans Protein Carbamylation - immunology Rheumatoid arthritis rheumatoid factor Rheumatoid Factor - immunology Sensitivity and Specificity |
Subtitle | Implications for Very Early Identification of At‐Risk Individuals |
Title | Triple Positivity for Anti–Citrullinated Protein Autoantibodies, Rheumatoid Factor, and Anti–Carbamylated Protein Antibodies Conferring High Specificity for Rheumatoid Arthritis |
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