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Abstract Number: 1319

Diagnostic Value Of Anti-Citrullinated Proteins Antibodies In Rheumatoid Arthritis

Claudia L. Giraldo1, Rafael Chaparro del Moral2, Mercedes Ciancio3,4, Oscar L. Rillo5, Emilia Saint Martin6, Emilce Schneeberger7, Gustavo Citera7, Federico Zazzetti8, Amalia Schiel9 and Juan C. Barreira10, 1Rheumatology, Hospital Gral. de Agudos Dr. E. Tornú, Buenos Aires, Argentina, 2Rheumatology Section, Hospital General de Agudos Dr. E. Tornú, Buenos Aires, Argentina, 3Hospital General de Agudos "Dr. E. Tornú", Buenos Aires, Argentina, 4Biochemestry, Buenos Aires, Argentina, 5Rheumatology, Hospital General de Agudos "Dr. E. Tornú", Buenos Aires, Argentina, 6Rheumatology, Instituto de Rehabilitacion Psicofisica, Buenos Aires, Argentina, 7Rheumatology, Instituto de Rehabilitación Psicofísica, Buenos Aires, Argentina, 8Rheumatology, Buenos Aires Hospital Britanico, Buenos Aires, Argentina, 9Central Laboratory, British Hospital, Buenos Aires, Argentina, 10Rheumatology, Buenos Aires British Hospital, Buenos Aires, Argentina

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: ACPA, anti-CCP antibodies and anti-mutated citrullinated vimentin

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Session Information

Title: Rheumatoid Arthritis - Clinical Aspects II: Predictors of Disease Course in Rheumatoid Arthritis - Treatment Approaches

Session Type: Abstract Submissions (ACR)

Background/Purpose: Citrulline and vimentin are some of the proteins used as antigens for anti-citrullinated proteins antibodies (ACPAs) detection for the diagnosis of rheumatoid arthritis (RA). In our country, anti-mutated citrullinated vimentin (anti-MCV) kit is 50% cheaper than the anti-cyclic citrullinated peptide (anti-CCP3) kit. The aim of our study was to evaluate the diagnostic value of anti-MCV compared to anti-CCP3 and rheumatoid factor (RF) and to explore the relationship between them and disease activity

Methods: Consecutive patients ≥ 18 years with RA (ACR 1987 and ACR/EULAR 2010 criteria) were included. The control group consisted of 73 subjects with undifferentiated arthritis, SLE, Psoriatic Arthritis, Sjögren’s Syndrome and Erosive Osteoarthritis (non RA arthritis). Anti-MCV and anti-CCP3 were determined by ELISA and RF by immunoturbidimetry. The cutoff value for the three methods was ≥ 20 IU/ml. Sensitivity (S), Specificity (E), Positive and Negative Predictive Values (PPV, NPV) and Likelihood Ratio (LR) of the RF, anti-CCP3 and anti-MCV were assessed using a two way table (Table). Binary logistic regression analyses were performed, using high disease activity (DAS28>5.1) as dependent variable. According to the RF, anti-CCP3 and anti-MCV concentrations, three groups of patients were obtained: low concentrations (under 25 percentile); intermediate concentrations (between 25 and 75 percentile) and high concentrations (above 75 percentile).The values of DAS28 for these three groups were compared by ANOVA and post-hoc tests

Results: 234 patients were evaluated (161 RA and 73 controls). In the RA group, 85% were female, the mean age was 53 (18-91) years, the median symptoms duration was 120 months (IQR 39-180) and 31(19%) were early RA patients (<2 years). Mean DAS28 was 3.6 (±1.5); and the median HAQ 0.75 (IQR 0.25-1.25). The median of RF was 104 IU/ml (IQR 35-225); anti-CCP3 180 IU/ml (IQR 95-210) and anti-MCV 300 IU (IQR 55-1000). Higher values of DAS28 were observed in the group of patients with RF > 225 IU/ml (mean DAS28 4.3 p = 0.006) and also in patients with anti-MCV > 1000 IU (DAS28 4.2 p=0.01). There were no differences for anti-CCP3. In early RA patients, a multivariate analysis (adjusted by symptom duration) showed that anti-MCV levels were associated with high disease activity. The OR estimated for the association between high disease activity and anti-MCV ≥ 1000 IU in early RA patients was 11.8 (CI 95%1.049-132.9). There was not significant association between RF, anti- MCV nor anti-CCP3 and DAS28 > 5.1 in established RA patients.                                                                           

Table.

 

         S

          E

       PPV

      NPV     

          LR

Anti-MCV

       93.4

       83.6

         93

        85

        5.69

Anti-CCP3

       83.7

       84.9

         93

        69

        5.54

RF

       84.9

       84.9

         93

        71

        5.62

Conclusion: In our study, anti-MCV compared to anti-CCP3 and RF had a higher sensitivity with equal specificity. We found increased RA activity in patients with higher titers of RF and anti-MCV


Disclosure:

C. L. Giraldo,
None;

R. Chaparro del Moral,
None;

M. Ciancio,
None;

O. L. Rillo,
None;

E. Saint Martin,
None;

E. Schneeberger,
None;

G. Citera,
None;

F. Zazzetti,
None;

A. Schiel,
None;

J. C. Barreira,
None.

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