Autoimmune diseases and autoantibodies in the first degree relatives of patients with systemic sclerosis

被引:53
作者
Arora-Singh, Rajpreet K. [1 ]
Assassi, Shervin [1 ]
del Junco, Deborah J. [2 ]
Arnett, Frank C. [1 ]
Perry, Marilyn [1 ]
Irfan, Uzma [1 ]
Sharif, Roozbeh [1 ]
Mattar, Tony [3 ]
Mayes, Maureen D. [1 ]
机构
[1] Univ Texas Houston, Hlth Sci Ctr, Div Rheumatol & Immunogenet, Houston, TX 77030 USA
[2] Univ Texas Houston, Hlth Sci Ctr, Ctr Clin & Translat Sci, Houston, TX 77030 USA
[3] Comp Task Force Inc, Troy, MI USA
关键词
Systemic sclerosis; Scleroderma; First degree relatives; ANA; Autoimmune disease; SINGLE-NUCLEOTIDE POLYMORPHISM; TYROSINE-PHOSPHATASE PTPN22; PERIPHERAL-BLOOD CELLS; LUPUS-ERYTHEMATOSUS; FUNCTIONAL POLYMORPHISM; ANTINUCLEAR ANTIBODIES; RHEUMATOID-ARTHRITIS; FAMILIAL OCCURRENCE; R620W POLYMORPHISM; GENE-EXPRESSION;
D O I
10.1016/j.jaut.2010.02.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Objective: To determine aggregation of autoimmune diseases in the first degree relatives (FDR) of patients with systemic sclerosis (SSc) and to investigate frequencies of antinuclear antibodies (ANA) and other autoantibodies in the FDRs and spouses of patients with SSc. Methods: Information on FDRs including history of autoimmune disease was obtained from unrelated SSc probands in the Scleroderma Family Registry and DNA Repository. FDRs were contacted to verify any reported autoimmune diseases. The prevalence of autoimmune disease in probands' families was compared with the corresponding prevalence in controls' families as reported in the literature. Furthermore, sera from probands' FDRs and spouses in addition to unrelated controls were investigated for the presence of autoantibodies (ANA). Results: We investigated 4612 FDRs of 1071 SSc probands. SSc probands with anti-centromere antibodies (ACA) and limited disease type were more likely to report familial autoimmunity (p = 0.022 and p = 0.041, respectively). The four most prevalent autoimmune diseases among SSc probands' FDRs were hypothyroidism (4%), Rheumatoid arthritis (1.5%), hyperthyroidism (1.3%) and systemic lupus erythematosus-SLE (0.4%). Compared to control families, SLE, hypothyroidism and hyperthyroidism were more common in SSc probands' families. The most striking increase for familial prevalence was observed in SLE (OR = 16.98, 95% CI = 1.02-227.82, p = 0.004). ANA was present in 14.2% of probands' FDR's and 8.6% of spouses and did not differ from the prevalence of ANA among controls (p = 0.124 and p = 0.477, respectively). Only two FDRs of probands had ACA while none had anti-topoisomerase antibodies. Conclusion: Our study implies varying degrees of risk for familial autoimmunity among subtypes of SSc and provides further support for common genetic and potentially environmental factors leading to SSc and SLE. (C) 2010 Published by Elsevier Ltd.
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收藏
页码:52 / 57
页数:6
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