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SAT0003 Relationship Between Anticitrullinated Protein Antibodies and Clinical Remission in Arthritis
  1. R. Hernandez1,
  2. P. Gonzalez2,
  3. A. Muñoz1,
  4. J. L. Marenco1
  1. 1Rheumatology, Valme University Hospital
  2. 2Rheumatology, Valme Hospital, Seville, Spain


Background The relationship between anticitrullinated protein antibodies (ACPA) and the clinical outcome of rheumatoid arthritis (RA) under treatment has been evaluated in clinical trials with conflicting results. Thus, an analysis of the BeSt study(1) indicated that response to treatment was similar in ACPA-positive and ACPA-negative patients However, ACPA-positive patients showed more frequently radiological damage progression. On the contrary, in the IMPROVED study(2), ACPA-negative patients achieved less remissions on treatment than ACPA-positive patients

Objectives We evaluated the clinical response of patients with RA receiving treatment according to ACPA titers.

Methods This was a retrospective longitudinal observational study. We included all patients seen at our Unit who fulfilled the following criteria: 1) Diagnosis of RA by a rheumatologist meeting the 1987 criteria for RA; 2) Available determinations of ACPA; 3) Treatment for AR (whether or not biological therapy) with a minimum follow up of 6 months. The outcome variable was clinical regression defined as reaching DAS28 <=2.6. Predictors of the outcome variable were evaluated using logistic regression models adjusted by gender and age.

Results 71 patients were included, 79% of them women. Clinical regression was observed in 42 (59%) patients during the first 12 months of follow-up. Baseline median (IQR) ACPA levels were 363 (27.7-500) for individuals without clinical regression and 91.7 (7-458) for those with regression (p=0.045). 19 (66%) patients without regression vs. 15 (36%) with regression showed ACPA levels ≥200 (p=0.013). 6 (20%) patients without clinical response vs. 18 (42%) individuals with response showed negative ACPA titers (p= 0.050). Factors independently associated with clinical regression were: Recent onset RA [adjusted odds ratio (AOR) 5; 95% confidence interval (95%CI) 1.01-25; p=0.049], baseline ACPA levels ≥200 [AOR 0.13; 95%CI 0.03-0.5; p=0.004], baseline CRP levels [per unit increase; AOR 0.94; 95%CI 0.91-0.99; p=0.024], baseline DAS28 [per unit increase; AOR 0.47; 95%CI 0.25-0.89; p=0.021].

Conclusions ACPA levels can predict clinical regression of patients with RA receiving treatment in real life conditions. Individuals with high ACPA levels may benefit from a more aggressive treatment approach. ACPA titers may be useful to monitor the clinical activity of RA.


  1. The association of treatment response and joint damage with ACPA-status in recent-onset RA: a subanalysis of the 8-year follow-up of the BeSt study. M van den Broek,1 L Dirven,1 NB Klarenbeek,1 THE Molenaar,2 Ann Rehum Dis 2012;71:245-248.

  2. Remission induction therapy with MTX and predinisone in patients with early rheumatoid and indifferentiated arthritis (yhe IMPROVED study)Ann Rheum Rheum Dis 2012 ;March 8

Disclosure of Interest None Declared

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