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 inArthritis & rheumatology (Hoboken, N.J.) Vol. 70; no. 11; pp. 1721 - 1731
Main Authors Verheul, Marije K., Böhringer, Stefan, van Delft, Myrthe A. M., Jones, Jonathan D., Rigby, William F. C., Gan, Ryan W., Holers, V. Michael, Edison, Jess D., Deane, Kevin D., Janssen, Koen M. J., Westra, Johanna, Brink, Mikael, Rantapää‐Dahlqvist, Solbritt, Huizinga, Tom W. J., van der Helm‐van Mil, Annette H. M., van der Woude, Diane, Toes, Rene E. M., Trouw, Leendert A.
Format Journal Article
LanguageEnglish
Published 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.
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.
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  organization: Geisel School of Medicine at Dartmouth Lebanon New Hampshire
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  organization: Geisel School of Medicine at Dartmouth Lebanon New Hampshire
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  organization: Colorado School of Public Health Aurora
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  organization: Walter Reed National Military Medical Center Bethesda Maryland
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  surname: Deane
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  organization: University of Colorado Aurora
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  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
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  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
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  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
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  givenname: Rene E. M.
  surname: Toes
  fullname: Toes, Rene E. M.
  organization: Leiden University Medical Center Leiden The Netherlands
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  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
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Cites_doi 10.1186/s13075-016-1001-6
10.1186/s13075-016-1192-x
10.1136/annrheumdis-2013-203650
10.1002/art.37830
10.1136/annrheumdis-2013-205109
10.1186/s13075-016-1173-0
10.1093/rheumatology/kev250
10.3899/jrheum.150179
10.1136/annrheumdis-2016-209991
10.3899/jrheum.130742
10.1111/j.0006-341X.1999.00597.x
10.1073/pnas.1114465108
10.1038/nrrheum.2017.185
10.1136/annrheumdis-2015-208870
10.1016/j.clim.2015.04.005
10.1038/s41598-017-09657-5
10.1002/art.40061
10.1136/annrheumdis-2017-211249
10.1136/annrheumdis-2015-207326
10.1186/s13075-015-0690-6
10.5114/reum.2017.66680
10.1016/j.autrev.2015.08.003
10.1007/s12026-014-8560-x
10.1002/art.27584
10.1136/annrheumdis-2013-204154
10.1136/annrheumdis-2015-207751
10.1186/s13075-016-0940-2
10.1038/nrrheum.2017.15
10.1186/s13075-015-0860-6
10.1016/j.autrev.2012.05.007
10.1136/annrheumdis-2016-209248
10.1371/journal.pone.0180144
10.7326/0003-4819-146-11-200706050-00008
10.1371/journal.pone.0159000
10.1136/annrheumdis-2014-206047
10.3899/jrheum.140767
10.1136/rmdopen-2015-000172
10.1136/ard.2008.105759
10.1002/art.1780310302
10.1093/rheumatology/kex088
10.1172/jci.insight.88912
10.1002/art.39664
10.1186/s13075-014-0515-z
10.1136/annrheumdis-2015-208579
10.1007/s00296-012-2458-5
10.1136/annrheumdis-2014-205227
10.3389/fimmu.2017.00285
10.1186/s13075-015-0536-2
10.1002/acr.22385
10.1016/j.jaut.2017.02.008
10.1371/journal.pone.0161141
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PublicationTitle Arthritis & rheumatology (Hoboken, N.J.)
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References e_1_2_7_5_1
e_1_2_7_3_1
e_1_2_7_9_1
e_1_2_7_7_1
e_1_2_7_19_1
e_1_2_7_17_1
Alessandri C (e_1_2_7_22_1) 2015; 33
e_1_2_7_15_1
e_1_2_7_41_1
e_1_2_7_13_1
e_1_2_7_43_1
e_1_2_7_11_1
e_1_2_7_45_1
e_1_2_7_47_1
e_1_2_7_26_1
e_1_2_7_49_1
e_1_2_7_50_1
e_1_2_7_25_1
e_1_2_7_31_1
e_1_2_7_52_1
e_1_2_7_23_1
e_1_2_7_33_1
e_1_2_7_54_1
e_1_2_7_21_1
e_1_2_7_35_1
e_1_2_7_37_1
e_1_2_7_39_1
e_1_2_7_6_1
e_1_2_7_4_1
e_1_2_7_8_1
e_1_2_7_18_1
e_1_2_7_16_1
e_1_2_7_40_1
e_1_2_7_2_1
e_1_2_7_14_1
e_1_2_7_42_1
e_1_2_7_12_1
e_1_2_7_44_1
e_1_2_7_10_1
e_1_2_7_46_1
e_1_2_7_48_1
e_1_2_7_27_1
e_1_2_7_29_1
Kumar S (e_1_2_7_28_1) 2017; 55
e_1_2_7_51_1
e_1_2_7_30_1
e_1_2_7_53_1
e_1_2_7_24_1
e_1_2_7_32_1
e_1_2_7_34_1
e_1_2_7_20_1
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References_xml – ident: e_1_2_7_46_1
  doi: 10.1186/s13075-016-1001-6
– ident: e_1_2_7_41_1
  doi: 10.1186/s13075-016-1192-x
– ident: e_1_2_7_39_1
  doi: 10.1136/annrheumdis-2013-203650
– ident: e_1_2_7_18_1
  doi: 10.1002/art.37830
– ident: e_1_2_7_26_1
  doi: 10.1136/annrheumdis-2013-205109
– ident: e_1_2_7_30_1
  doi: 10.1186/s13075-016-1173-0
– ident: e_1_2_7_54_1
  doi: 10.1093/rheumatology/kev250
– ident: e_1_2_7_24_1
  doi: 10.3899/jrheum.150179
– ident: e_1_2_7_3_1
  doi: 10.1136/annrheumdis-2016-209991
– ident: e_1_2_7_34_1
  doi: 10.3899/jrheum.130742
– ident: e_1_2_7_44_1
  doi: 10.1111/j.0006-341X.1999.00597.x
– ident: e_1_2_7_14_1
  doi: 10.1073/pnas.1114465108
– ident: e_1_2_7_51_1
  doi: 10.1038/nrrheum.2017.185
– ident: e_1_2_7_20_1
  doi: 10.1136/annrheumdis-2015-208870
– ident: e_1_2_7_13_1
  doi: 10.1016/j.clim.2015.04.005
– ident: e_1_2_7_50_1
  doi: 10.1038/s41598-017-09657-5
– ident: e_1_2_7_53_1
  doi: 10.1002/art.40061
– ident: e_1_2_7_52_1
  doi: 10.1136/annrheumdis-2017-211249
– ident: e_1_2_7_25_1
  doi: 10.1136/annrheumdis-2015-207326
– ident: e_1_2_7_35_1
  doi: 10.1186/s13075-015-0690-6
– volume: 55
  start-page: 4
  year: 2017
  ident: e_1_2_7_28_1
  article-title: Assessment of anti‐CarP antibodies, disease activity and quality of life in rheumatoid arthritis patients on conventional and biological disease‐modifying antirheumatic drugs
  publication-title: Reumatologia
  doi: 10.5114/reum.2017.66680
– ident: e_1_2_7_38_1
  doi: 10.1016/j.autrev.2015.08.003
– ident: e_1_2_7_33_1
  doi: 10.1007/s12026-014-8560-x
– ident: e_1_2_7_43_1
– ident: e_1_2_7_2_1
  doi: 10.1002/art.27584
– ident: e_1_2_7_17_1
  doi: 10.1136/annrheumdis-2013-204154
– ident: e_1_2_7_40_1
  doi: 10.1136/annrheumdis-2015-207751
– ident: e_1_2_7_8_1
  doi: 10.1186/s13075-016-0940-2
– ident: e_1_2_7_12_1
  doi: 10.1038/nrrheum.2017.15
– ident: e_1_2_7_42_1
  doi: 10.1186/s13075-015-0860-6
– ident: e_1_2_7_7_1
  doi: 10.1016/j.autrev.2012.05.007
– ident: e_1_2_7_36_1
  doi: 10.1136/annrheumdis-2016-209248
– ident: e_1_2_7_32_1
  doi: 10.1371/journal.pone.0180144
– ident: e_1_2_7_6_1
  doi: 10.7326/0003-4819-146-11-200706050-00008
– ident: e_1_2_7_48_1
  doi: 10.1371/journal.pone.0159000
– ident: e_1_2_7_11_1
  doi: 10.1136/annrheumdis-2014-206047
– ident: e_1_2_7_15_1
  doi: 10.3899/jrheum.140767
– ident: e_1_2_7_21_1
  doi: 10.1136/rmdopen-2015-000172
– ident: e_1_2_7_10_1
  doi: 10.1136/ard.2008.105759
– ident: e_1_2_7_47_1
  doi: 10.1002/art.1780310302
– ident: e_1_2_7_29_1
  doi: 10.1093/rheumatology/kex088
– ident: e_1_2_7_49_1
  doi: 10.1172/jci.insight.88912
– ident: e_1_2_7_27_1
  doi: 10.1002/art.39664
– ident: e_1_2_7_45_1
  doi: 10.1186/s13075-014-0515-z
– ident: e_1_2_7_19_1
  doi: 10.1136/annrheumdis-2015-208579
– ident: e_1_2_7_4_1
  doi: 10.1007/s00296-012-2458-5
– ident: e_1_2_7_9_1
  doi: 10.1136/annrheumdis-2014-205227
– ident: e_1_2_7_23_1
  doi: 10.3389/fimmu.2017.00285
– volume: 33
  start-page: 824
  year: 2015
  ident: e_1_2_7_22_1
  article-title: Anti‐carbamylated protein antibodies in unaffected first‐degree relatives of rheumatoid arthritis patients: lack of correlation with anti‐cyclic citrullinated protein antibodies and rheumatoid factor
  publication-title: Clin Exp Rheumatol
– ident: e_1_2_7_16_1
  doi: 10.1186/s13075-015-0536-2
– ident: e_1_2_7_5_1
  doi: 10.1002/acr.22385
– ident: e_1_2_7_31_1
  doi: 10.1016/j.jaut.2017.02.008
– ident: e_1_2_7_37_1
  doi: 10.1371/journal.pone.0161141
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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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