Skip Navigation


Rheumatology Advance Access originally published online on April 16, 2003
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
42/8/972    most recent
keg268v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (21)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Salvador, G.
Right arrow Articles by Sanmarti, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Salvador, G.
Right arrow Articles by Sanmarti, R.
Related Collections
Right arrow Rheumatoid Arthritis
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Rheumatology 2003; 42: 972-975
© 2003 British Society for Rheumatology

Prevalence and clinical significance of anti-cyclic citrullinated peptide and antikeratin antibodies in palindromic rheumatism. An abortive form of rheumatoid arthritis?

G. Salvador, A. Gomez, O. Viñas1, G. Ercilla1, J. D. Cañete, J. Muñoz-Gomez and R. Sanmarti

Hospital Clínic, Rheumatology and
1 Hospital Clínic, Immunology, Barcelona, Barcelona, Spain

Objective. To analyse the prevalence and clinical significance of anti-cyclic citrullinated peptide antibodies (anti-CCP) and antikeratin antibodies (AKA) in patients with palindromic rheumatism (PR).

Method. Sixty-three patients with PR were included: 33 were defined as pure or persistent PR at the time of serum test measurement, and 30 as associated PR, defined as patients with past history of PR who had developed persistent arthritis at the time of serum test: [21 with rheumatoid arthritis (RA)]. Sixty patients with early RA, and 80 with seronegative spondyloarthropathy were included as control groups. Anti-CCP were determined by a standardized ELISA test and AKA by indirect immunofluorescence in rat oesophagus. Clinical characteristics of these pure PR patients were compared according to the presence or absence of anti-CCP antibodies. A follow-up study was also performed.

Results. Anti-CCP were detected in 18 out of 32 (56.3%) patients with pure PR and 10 out of 30 (33.3%) with associated PR (38.1% in RA-associated PR patients). AKA were detected in 12 patients out of 33, with pure PR (36.4%), and in 9 out of 30 with associated PR (30%) (33.3% in RA-associated PR patients). The prevalence of anti-CCP and AKA in the RA control group was 55% (not significantly different from the pure PR group) and 61.7% (with respect to pure PR patients, P=0.02), respectively. In the spondyloarthropathy group, the prevalence of anti-CCP and AKA was 2.5 and 3.8%, respectively (P<0.001 compared with pure PR patients). No significant clinical differences were observed between pure PR patients with and without CCP antibodies.

Conclusions. Anti-CCP and, to a lesser extent, AKA, were found in a high proportion of patients with PR, suggesting that this syndrome is an abortive form of RA. The predictive value of these antibodies in PR, as markers of progression to an established RA, remains uncertain.

KEY WORDS: Palindromic rheumatism, Anti-CCP antibodies, Antikeratin antibodies, AKA, Rheumatoid arthritis.

Correspondence to: R. Sanmarti, Hospital Clínic, Rheumatology, Barcelona, Barcelona, Spain. E-mail: sanmarti{at}clinic.ub.es


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Rheumatology (Oxford)Home page
G. Orozco, D. Pascual-Salcedo, M. A. Lopez-Nevot, T. Cobo, A. Cabezon, E. Martin-Mola, A. Balsa, and J. Martin
Auto-antibodies, HLA and PTPN22: susceptibility markers for rheumatoid arthritis
Rheumatology, February 1, 2008; 47(2): 138 - 141.
[Abstract] [Full Text] [PDF]


Home page
Ann Rheum DisHome page
F. Dubois-Galopin, C. Beauvillain, D. Dubois, A. Pillet, G. Renier, P. Jeannin, C. Masson, and A. Chevailler
New markers and an old phenomenon: prozone effect disturbing detection of filaggrin (keratin) autoantibodies
Ann Rheum Dis, August 1, 2007; 66(8): 1121 - 1122.
[Full Text] [PDF]


Home page
Rheumatology (Oxford)Home page
A. J. W. Zendman, W. J. van Venrooij, and G. J. M. Pruijn
Use and significance of anti-CCP autoantibodies in rheumatoid arthritis
Rheumatology, January 1, 2006; 45(1): 20 - 25.
[Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.