Guest guest Posted January 18, 2011 Report Share Posted January 18, 2011 Rheumatology (2011) 50 (2): 248-249. Which elements of the criteria for RA are stable over time? Leendert A. Trouw1 and Tom W. J. Huizinga1 1Department of Rheumatology, C1-R, Leiden University Medical Center, Leiden, The Netherlands Accepted July 12, 2010. Low seroconversion rate of anti-CCP2 and RF in early inflammatory arthritis This editorial refers to ‘Lack of seroconversion of rheumatoid factor and anti-cyclic citrullinated peptide in patients with early inflammatory arthritis: a systematic literature review’, by Lillian Barra et al., doi:10.1093/rheumatology/keq190, on page 311. Early diagnosis of RA is increasingly recognized as an essential step towards better patient care. Detection of autoantibodies such as RF and especially ACPA have proved valuable for early identification of patients with early arthritis at risk of developing RA [1]. The presence of ACPA has been shown to be predictive of development of RA [2] and associates with more severe diseases [3], suggesting a possible pathogenic role for these autoantibodies. Functional studies also implicate such a role as ACPA can trigger Fc receptors on inflammatory cells [4] and can activate the complement system [5]. Data derived from mouse studies confirm the hypothesis that ACPA may be pathogenic [6, 7]. Prediction rules and new criteria have been developed to diagnose RA earlier [8, 9]. These prediction rules are based on the 1987 RA criteria [10], which define a phenotype on which most of our pathophysiological studies are based. It has now become clear that this phenotype consists of two syndromes: ACPA-positive and ACPA-negative disease that differ by genetic risk factors, histology, clinical course and response to treatment [11–15]. The new criteria are partly based on the decision to start MTX therapy, which allows the inclusion of a much more heterogeneous phenotype [8]. ****************************************** Read the full editorial here: http://rheumatology.oxfordjournals.org/content/50/2/248.full?etoc Not an MD Quote Link to comment Share on other sites More sharing options...
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