4.7 Article

Zinc Transporter 8 Antibodies Complement GAD and IA-2 Antibodies in the Identification and Characterization of Adult-Onset Autoimmune Diabetes Non Insulin Requiring Autoimmune Diabetes (NIRAD) 4

Journal

DIABETES CARE
Volume 33, Issue 1, Pages 104-108

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dc08-2305

Keywords

-

Funding

  1. European Union [FP7-HEALTH-2007, N202013]
  2. Research Foundation of Societa Italiana di Diabetologia
  3. Novo Nordisk, Italy

Ask authors/readers for more resources

OBJECTIVE - Zinc transporter 8 (ZnT8) is an islet beta-cell secretory granule membrane protein recently identified as an autoantibody antigen in type 1 diabetes. The aim of this Study was to determine the prevalence and role of antibodies to ZnT8 (ZnT8As) in adult-onset diabetes. RESEARCH DESIGN AND METHODS - ZnT8As were measured by a radioimmuno-precipitation assay using recombinant ZnT8 COOH-terminal or NH2-terminal proteins in 193 patients with adult-onset autoimmune diabetes having antibodies to either GAD (GADAs) or IA-2 (IA-2As) and in 1,056 antibody-negative patients with type 2 diabetes from the Non Insulin Requiring Autoimmune Diabetes (NIRAD) study. RESULTS - ZnT8As-COOH were detected in 18.6% patients with autoimmune diabetes and 1.4% with type 2 diabetes. ZnT8As-NH2 were rare. ZnT8As were associated with younger age and a high GADA titer. The use of GADAs, IA-2As, and ZnT8As in combination allowed a stratification of clinical phenotype, with younger age of onset of diabetes and characteristics of more severe insulin deficiency (higher fasting glucose and A1C, lower BMI, total cholesterol, and triglycerides) in patients with all three markers, with progressive attenuation in patients With two, one, and no antibodies (all P-trend < 0.001). Autoantibody titers, association with high-risk HLA genotypes and prevalence of, thyroid peroxidase antibodies followed the same trend (all P < 0.001). CONCLUSIONS - ZnT8As are detectable in a proportion of patients With adult-onset autoimmune diabetes and seem to be a valuable marker to differentiate clinical phenotypes.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available