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      Organ-specific autoantibodies and autoimmune diseases in juvenile systemic lupus erythematosus and juvenile dermatomyositis patients

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      Pediatric Rheumatology Online Journal
      BioMed Central
      2011 Pediatric Rheumatology Symposium sponsored by the American College of Rheumatology
      2-5 June 2011

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          Abstract

          Purpose The purpose of this study was to evaluate organ-specific autoantibodies and autoimmune diseases in JSLE and JDM patients. Methods Forty-one JSLE and 41 JDM patients were investigated for serum autoantibodies associated with autoimmune hepatitis, primary biliary cirrhosis, type 1 diabetes mellitus (T1DM), autoimmune thyroiditis, autoimmune gastritis and celiac disease. Patients with positive organ-specific antibodies were assessed for the presence of the respective organ-specific autoimmune diseases. Results Mean age at diagnosis was significantly higher in JSLE compared to JDM patients (10.3±3.4 vs. 7.3±3.1years, p=0.0001), whereas the mean disease duration was similar in both groups. The frequencies of organ-specific autoantibodies were similar between JSLE and JDM (p>0.05). Of note, a high prevalence of autoantibodies related to DM1 and autoimmune thyroiditis was observed in both groups (20% vs. 15%, p=0.77 and 24% vs. 15%, p=0.41; respectively). Higher frequencies of antinuclear antibody - ANA (93% vs. 59%, p=0.0006), anti-dsDNA (61% vs. 2%, p<0.0001), anti-Ro (35% vs. 0%, p<0.0001), anti-Sm (p=0.01), anti-RNP (p=0.02), anti-La (p=0.03) and IgG aCL (p=0.001) were observed in JSLE compared to JDM patients. Organ-specific autoimmune diseases were evidenced only in JSLE patients (24% vs. 0%, p=0.13). Two JSLE patients had T1DM associated with Hashimoto thyroiditis and another had subclinical thyroiditis. Other JSLE patient had celiac disease diagnosis based on iron deficiency anaemia, presence of anti-endomysial antibody, duodenal biopsy compatible to celiac disease and response to a gluten-free diet. Conclusion Organ-specific diseases were observed solely in JSLE patients and required specific therapy. The presence of these antibodies recommends the evaluation of organ-specific diseases and a rigorous follow-up of these patients. Disclosure Nadia E. Aikawa: None; Adriana A. Jesus: None; Bernadete L. Liphaus: None; Bernadete L. Liphaus: None; Clovis A. Silva: None; Magda C. Sampaio: None; Adriana M. Sallum: None.

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          Author and article information

          Conference
          Pediatr Rheumatol Online J
          Pediatr Rheumatol Online J
          Pediatric Rheumatology Online Journal
          BioMed Central
          1546-0096
          2012
          13 July 2012
          : 10
          : Suppl 1
          : A14
          Affiliations
          [1 ]University of São Paulo, Sao Paulo, Brazil
          Article
          1546-0096-10-S1-A14
          10.1186/1546-0096-10-S1-A14
          3403049
          eb4fd519-75a9-468f-8ad9-72c3dbcb5d9d
          Copyright ©2012 Aikawa et al; licensee BioMed Central Ltd.

          This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

          2011 Pediatric Rheumatology Symposium sponsored by the American College of Rheumatology
          Miami, FL, USA
          2-5 June 2011
          History
          Categories
          Poster Presentation

          Pediatrics
          Pediatrics

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