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Specific association of type 1 diabetes mellitus with anti-cyclic citrullinated peptide-positive rheumatoid arthritis

Authors :
Robert M. Plenge
Johan Askling
Bo Ding
Lars Klareskog
Lars Alfredsson
Henrik Källberg
Elizabeth W. Karlson
Katherine P. Liao
Marie Gunnarsson
Leonid Padyukov
Source :
Arthritis and rheumatism. 60(3)
Publication Year :
2009

Abstract

Objective The co-occurrence of autoimmune diseases such as rheumatoid arthritis (RA) and type 1 diabetes mellitus (DM) has been reported in individuals and families. In this study, the strength and nature of this association were investigated at the population level in a Swedish case–control cohort. Methods For this case–control study, 1,419 patients with incident RA diagnosed between 1996 and 2003 were recruited from university, public, and private rheumatology units throughout Sweden; 1,674 matched control subjects were recruited from the Swedish national population registry. Sera from the subjects were tested for the presence of antibodies to cyclic citrullinated peptide (anti-CCP), rheumatoid factor (RF), and the 620W PTPN22 allele. Information on a history of diabetes was obtained by questionnaire, telephone interview, and/or medical record review. The prevalence of type 1 DM and type 2 DM was compared between patients with incident RA and control subjects and further stratified for the presence of anti-CCP, RF, and the PTPN22 risk allele. Results Type 1 DM was associated with an increased risk of RA (odds ratio [OR] 4.9, 95% confidence interval [95% CI] 1.8–13.1), and this association was specific for anti-CCP–positive RA (OR 7.3, 95% CI 2.7–20.0), but not anti-CCP–negative RA. Further adjustment for the presence of PTPN22 attenuated the risk of anti-CCP–positive RA in patients with type 1 DM to an OR of 5.3 (95% CI 1.5–18.7). No association between RA and type 2 DM was observed. Conclusion The association between type 1 DM and RA is specific for a particular RA subset, anti-CCP–positive RA. The risk of developing RA later in life in patients with type 1 DM may be attributed, in part, to the presence of the 620W PTPN22 allele, suggesting that this risk factor may represent a common pathway for the pathogenesis of these 2 diseases.

Details

ISSN :
00043591
Volume :
60
Issue :
3
Database :
OpenAIRE
Journal :
Arthritis and rheumatism
Accession number :
edsair.doi.dedup.....34808806aec850145c174b20685854e7