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. 2024 Apr 10;10(2):e003927.
doi: 10.1136/rmdopen-2023-003927.

Utility of testing for third-generation anticyclic citrullinated peptide (anti-CCP3) antibodies in individuals who present with new musculoskeletal symptoms but have a negative second-generation anticyclic citrullinated peptide (anti-CCP2) antibody test

Andrea Di Matteo  1   2 , Kulveer Mankia  1   2 , Leticia Garcia-Montoya  1   2 , Sana Sharrack  3 , Laurence Duquenne  1   2 , Jacqueline L Nam  4 , Michael Mahler  5 , Paul Emery  6   2
Affiliations

Utility of testing for third-generation anticyclic citrullinated peptide (anti-CCP3) antibodies in individuals who present with new musculoskeletal symptoms but have a negative second-generation anticyclic citrullinated peptide (anti-CCP2) antibody test

Andrea Di Matteo et al. RMD Open. .

Abstract

Objectives: To investigate the role of third-generation anticyclic citrullinated peptide (anti-CCP3) antibodies in predicting progression to inflammatory arthritis (IA) in individuals with new musculoskeletal (MSK) symptoms and a negative second-generation anti-CCP antibody test (anti-CCP2-).

Methods: 469 anti-CCP2- individuals underwent baseline anti-CCP3 testing (QUANTA Lite CCP3; Inova Diagnostics) and received a post enrolment 12-month questionnaire. A rheumatologist confirmed or excluded diagnosis of IA. Univariable/multivariable analyses were performed to assess the value of anti-CCP3 in predicting IA development in these anti-CCP2- individuals.

Results: Only 16/469 (3.4%) anti-CCP2- individuals had a positive anti-CCP3 test. Of these 16 individuals, 4 developed IA. In addition, 61/469 (13.0%) anti-CCP2- individuals self-reported, to have developed, IA. Progression was confirmed in 43/61 of them (70.5%); of whom 30/43 (69.8%) and 13/43 (30.2%) were given a diagnosis of IA and rheumatoid arthritis (RA), respectively. In qualitative univariable analysis, anti-CCP3 positivity was associated with self-reported progression (p<0.01) and IA (p=0.03), but not with RA. Anti-CCP3 levels differed significantly between progressors and non-progressors (p<0.01) for all three categories. At the manufacturer's cut-off, OR for progression ranged from 2.4 (95% CI 0.5 to 18.6; RA) to 7.5 (95% CI 2.3 to 24.0; self-reported progression). Interestingly, when cut-offs for anti-CCP3 were optimised, lower values (≥5 units) significantly increased the OR for progression in all three categories. In multivariable analysis, anti-CCP3 positivity at the manufacturer's cut-off did not remain associated with IA progression, while this lower cut-off value (≥5 units) was associated with diagnosis of RA (p=0.02).

Conclusions: Anti-CCP3 testing could improve the prediction of IA development in anti-CCP2- individuals with new MSK symptoms.

Keywords: Anti-Citrullinated Protein Antibodies; Antibodies; Arthritis, Rheumatoid.

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Conflict of interest statement

Competing interests: ADM has received speaking fees from Janssen. KM reports personal fees from Abbvie, Lilly, Galapagos, UCB and Serac Healthcare outside the submitted work and research grants from Gilead, Serac Healthcare and Lilly. MM is employed at Werfen, a diagnostic company that commercialises the CCP3 assay. He does not have stocks or shares of the company or other incentives for the product. Testing was done at the University of Leeds and MM was not involved. PE reports providing expert advice to Abbvie, Astra-Zeneca, BMS, Boehringer Ingelheim, Galapagos, Gilead, Lilly, Novartis, Pfizer, Roche, Samsung outside the submitted work. He also reports research grants from AbbVie, BMS, Lilly and Samsung. The remaining authors have declared no conflicts of interest.

Figures

Figure 1
Figure 1
Schematic representation of the study design. *Refers to reference n=21; **refers to reference n=25. +ve, positive; −ve, negative; Ab, antibodies; CCP, cyclic citrullinated peptide; IA, inflammatory arthritis.
Figure 2
Figure 2
Impact of anti-CCP3 antibody levels in predicting progression to inflammatory arthritis (IA). Anti-CCP3 antibody levels were significantly higher in individuals who progressed. (A–C) The titre differences in individuals who progressed (1; orange dots) to the non-progressors (0; blue dots). The blue and orange shaded areas indicate the distribution of anti-CCP3 results in progressors (orange) and non-progressors (blue). (A) Self-reported progression (B) IA/rheumatoid arthritis (RA) confirmed by a rheumatologist and (C) RA confirmed by a rheumatologist. (D–F) The ROC curves of anti-CCP3 antibodies in the three categories (self-reported progression, rheumatologist-confirmed diagnosis of IA or rheumatologist-confirmed diagnosis of RA). Lastly, (G–L) the corresponding pre-test and post-test probability curves at the optimised cut-off. IA includes patients with RA. CCP3, third-generation anticyclic citrullinated peptide antibodies; C/O, cut-off; ROC, receiver operating characteristic.
Figure 3
Figure 3
Ability of anti-CCP3 antibody status (qualitative) in predicting progression to inflammatory arthritis (IA). (A–C) Using the manufacturer’s cut-off values, anti-CCP3 antibody positivity was significantly higher in individuals who progressed by self-reported progression and IA diagnosis confirmed by a rheumatologist. (D–F) At optimised cut-off values (≥5 units), the difference in anti-CCP3 antibody positivity became more pronounced and also reached significance for RA diagnosis confirmed by a rheumatologist. IA includes patients with RA. CCP3, third-generation anticyclic citrullinated peptide antibodies; RA, rheumatoid arthritis; 1, positive; 0, negative.
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References

    1. Kolfenbach JR, Deane KD, Derber LA, et al. . Autoimmunity to Peptidyl arginine Deiminase type 4 precedes clinical onset of rheumatoid arthritis. Arthritis Rheum 2010;62:2633–9. 10.1002/art.27570 - DOI - PMC - PubMed
    1. Sokolove J, Bromberg R, Deane KD, et al. . Autoantibody EPITOPE spreading in the pre-clinical phase predicts progression to rheumatoid arthritis. PLoS One 2012;7:e35296. 10.1371/journal.pone.0035296 - DOI - PMC - PubMed
    1. Verheul MK, Böhringer S, van Delft MAM, et al. . 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. Arthritis Rheumatol 2018;70:1721–31. 10.1002/art.40562 - DOI - PubMed
    1. Kelmenson LB, Wagner BD, McNair BK, et al. . Timing of elevations of autoantibody isotypes prior to diagnosis of rheumatoid arthritis. Arthritis Rheumatol 2020;72:251–61. 10.1002/art.41091 - DOI - PMC - PubMed
    1. van Steenbergen HW, Aletaha D, Beaart-van de Voorde LJJ, et al. . EULAR definition of arthralgia suspicious for progression to rheumatoid arthritis. Ann Rheum Dis 2017;76:491–6. 10.1136/annrheumdis-2016-209846 - DOI - PubMed

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