Etiological Approach to Characterization of Diabetes Type

Author:

Dabelea Dana1,Pihoker Catherine2,Talton Jennifer W.3,D’Agostino Ralph B.3,Fujimoto Wilfred4,Klingensmith Georgeanna J.5,Lawrence Jean M.6,Linder Barbara7,Marcovina Santica M.8,Mayer-Davis Elizabeth J.9,Imperatore Giuseppina10,Dolan Lawrence M.11,

Affiliation:

1. Department of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Aurora, Colorado

2. Department of Washington, University of Washington, Seattle, Washington

3. Department of Biostatistical Sciences, Wake Forest University, School of Medicine, North Carolina

4. Kuakini Medical Center, Honolulu, Hawaii

5. Barbara Davis Center and Department of Pediatrics, University of Colorado Denver, School of Medicine, Aurora, Colorado

6. Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California

7. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland

8. Department of Medicine, University of Washington, Seattle, Washington

9. Departments of Nutrition and Medicine, University of North Carolina, Chapel Hill, North Carolina

10. Division of Diabetes Translation, Centers for Diseases Control and Prevention, Atlanta, Georgia

11. Department of Pediatrics, Cincinnati Children’s Hospital, University of Cincinnati College of Medicine, Cincinnati, Ohio

Abstract

OBJECTIVE To describe an etiologic approach to classification of diabetes types in youth based on the 1997 American Diabetes Association (ADA) framework, using data from the SEARCH for Diabetes in Youth Study. RESEARCH DESIGN AND METHODS SEARCH conducted a comprehensive assessment of 2,291 subjects aged <20 years with recently diagnosed diabetes. Using autoimmunity (at least one of two diabetes autoantibodies) and insulin sensitivity (equation validated against hyperinsulinemic-euglycemic clamps) as the main etiologic markers, we described four categories along a bidimensional spectrum: autoimmune plus insulin-sensitive (IS), autoimmune plus insulin-resistant (IR), nonautoimmune plus IS, and nonautoimmune plus IR. We then explored how characteristics, including genetic susceptibility to autoimmunity (HLA genotypes), insulin deficiency, and clinical factors varied across these four categories. RESULTS Most subjects fell into either the autoimmune plus IS (54.5%) or nonautoimmune plus IR categories (15.9%) and had characteristics that align with traditional descriptions of type 1 or type 2 diabetes. The group classified as autoimmune plus IR (19.5%) had similar prevalence and titers of diabetes autoantibodies and similar distribution of HLA risk genotypes to those in the autoimmune plus IS group, suggesting that it includes individuals with type 1 diabetes who are obese. The group classified as nonautoimmune plus IS (10.1%) likely includes individuals with undetected autoimmunity but may also include those with monogenic diabetes and thus requires further testing. CONCLUSIONS The SEARCH study offers researchers and clinicians a practical application for the etiologic classification of diabetes type and at the same time identifies a group of youths who would benefit from further testing.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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