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Published online May 16, 2008
Diabetes Care 31:1602-1607, 2008
DOI: 10.2337/dc08-0235
© 2008 by the American Diabetes Association
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Pathophysiology/Complications
Original Research

GAD65 Autoantibody Responses in Japanese Latent Autoimmune Diabetes in Adult Patients

Taro Maruyama, MD, PHD1, Shilpa Oak, PHD2, Akira Shimada, MD, PHD3 and Christiane S. Hampe, PHD2

1 Department of Internal Medicine, Saitama Social Insurance Hospital, Saitama, Japan
2 Department of Medicine, University of Washington, Seattle, Washington
3 Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan

Corresponding author: Christiane S. Hampe, champe{at}u.washington.edu

OBJECTIVE—To determine whether development of insulin requirement in patients with latent autoimmune diabetes in adults (LADA) is accompanied with the emergence of a type 1 diabetes–like autoimmune response.

RESEARCH DESIGN AND METHODS—We correlated β-cell–specific autoimmunity reflected in autoantibodies to the 65-kDa isoform of GAD (GAD65) with insulin requirement. We determined GAD65Ab epitope specificities in type 1 diabetic patients, LADA patients without insulin requirement (nonprogressed), and LADA patients that had developed insulin requirement (progressed).

RESULTS—Recognition of a type 1 diabetes–specific GAD65Ab epitope was more pronounced in type 1 diabetic patients than in nonprogressed (P < 0.001) or progressed (P < 0.01) LADA patients, with no significant differences between the two LADA cohorts. These differences were particularly pronounced in samples with GAD65Ab titers <1,000 units/ml, with no differences in epitope specificities in samples with higher GAD65Ab titers. Disease duration (initial diabetes diagnosis until sample collection or development of insulin requirement) in nonprogressed and progressed LADA patients, respectively, was not correlated with epitope specificity, suggesting lack of epitope maturation. This was supported by epitope analyses of longitudinal samples from LADA patients during progression to insulin requirement.

CONCLUSIONS—First, the GAD65Ab-specific autoimmune reaction in type 1 diabetic patients with low and moderate GAD65Ab titers differs from that in LADA patients, irrespective of insulin requirement. Second, the GAD65Ab-specific autoimmune response in LADA patients does not change after their initial diabetes diagnosis. Finally, LADA patients with high GAD65Ab titers resemble type 1 diabetic patients in their GAD65Ab epitope specificity.


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