Autoantibody “Subspecificity” in Type 1 Diabetes
Risk for organ-specific autoimmunity clusters in distinct groups
- Jennifer M. Barker, MD1,
- Jeesuk Yu, MD2,
- Liping Yu, MD1,
- Jian Wang, MD1,
- Dongmei Miao, MD1,
- Fei Bao, MD3,
- Edward Hoffenberg, MD4,
- Jerald C. Nelson, MD5,
- Peter A. Gottlieb, MD1,
- Marian Rewers, MD, PHD1 and
- George S. Eisenbarth, MD, PHD1
- 1Barbara Davis Center, University of Colorado Health Sciences Center, Denver, Colorado
- 2Department of Pediatrics, Dankook University Hospital, Cheonan, Korea
- 3Department of Pathology, Louisiana State University Health Sciences Center, School of Medicine, Shreveport, Louisiana
- 4The Children’s Hospital, Denver, Colorado
- 5Department of Medicine and Pathology, Loma Linda University School of Medicine, Loma Linda, California
- Address correspondence and reprint requests to Jennifer M. Barker, Barbara Davis Center, University of Colorado Health Sciences Center, 4200 E. 9th Ave., B140, Denver, CO 80262. E-mail: jennifer.barker{at}uchsc.edu
Abstract
OBJECTIVE—Autoimmune thyroid disease (AIT), celiac disease, and Addison’s disease are characterized by the presence of autoantibodies: thyroid peroxidase antibody (TPOAb) and thyroglobulin antibody (TGAb) in AIT, tissue transglutaminase antibody (TTGAb) in celiac disease, and 21-hydroxylase antibody (21-OHAb) in Addison’s disease. The objective of this study was to define the prevalence of these autoantibodies and clinical disease in a population with type 1 diabetes.
RESEARCH DESIGN AND METHODS—We screened 814 individuals with type 1 diabetes for TPOAb, TGAb, TTGAb, and 21-OHAb. Clinical disease was defined by chart review. Factors related to the presence of autoimmunity and clinical disease including age at onset of type 1 diabetes, duration of diabetes, age at screening, sex, and the presence of autoantibodies were reviewed.
RESULTS—The most common autoantibodies expressed were TPOAb and/or TGAb (29%), followed by TTGAb (10.1%) and 21-OHAb (1.6%). Specific HLA DR/DQ genotypes were associated with the highest risk for expression of 21-OHAb (DRB1*0404-DQ8, DR3-DQ2) and TTGAb (DR3-DQ2- DR3-DQ2). The expression of thyroid autoantibodies was related to 21-OHAb but not to TTGAb. The presence of autoantibodies was associated with and predictive of disease.
CONCLUSIONS—In this large cohort of individuals with type 1 diabetes, the expression of organ-specific autoantibodies was very high. The grouping of autoantibody expression suggests common factors contributing to the clustering.
- 21-OHAb, 21-hydroxylase antibody
- AIT, autoimmune thyroid disease
- ICA, islet cell antigen
- ICMA, immunochemiluminometric assay
- mIAA, microinsulin autoantibody assay
- TGAb, thyroglobulin antibody
- TPOAb, thyroid peroxidase antibody
- TSH, thyroid-stimulating hormone
- TTGAb, tissue transglutaminase antibody
Footnotes
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A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.
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- Accepted December 20, 2004.
- Received August 25, 2004.
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