Specific Association of Type 1 Diabetes Mellitus With Anti-Cyclic Citrullinated Peptide-Positive Rheumatoid Arthritis

被引:64
作者
Liao, Katherine P. [1 ]
Gunnarsson, Marie [2 ]
Kallberg, Henrik [2 ]
Ding, Bo
Plenge, Robert M. [3 ,4 ]
Padyukov, Leonid [2 ,5 ]
Karlson, Elizabeth W.
Klareskog, Lars [2 ,5 ,6 ]
Askling, Johan [2 ,5 ]
Alfredsson, Lars [2 ]
机构
[1] Brigham & Womens Hosp, Div Rheumatol Allergy & Immunol, Boston, MA 02115 USA
[2] Karolinska Inst, Stockholm, Sweden
[3] MIT, Cambridge, MA 02139 USA
[4] Harvard Univ, Cambridge, MA 02138 USA
[5] Karolinska Hosp, S-10401 Stockholm, Sweden
[6] Stockholm Cty Council, Stockholm Ctr Publ Hlth, Stockholm, Sweden
来源
ARTHRITIS AND RHEUMATISM | 2009年 / 60卷 / 03期
基金
英国医学研究理事会;
关键词
SHARED EPITOPE ALLELES; AUTOIMMUNE-DISEASES; RISK LOCUS; GENE; PTPN22; SUSCEPTIBILITY; SMOKING; POPULATION; PADI4; CLASSIFICATION;
D O I
10.1002/art.24362
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. The co-occurrence of autoimmune diseases such as rheumatoid arthritis (RA) and type I 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 I 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 I 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 I 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 I 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.
引用
收藏
页码:653 / 660
页数:8
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