Adult-Onset Autoimmune Diabetes in Europe Is Prevalent With a Broad Clinical Phenotype

التفاصيل البيبلوغرافية
العنوان: Adult-Onset Autoimmune Diabetes in Europe Is Prevalent With a Broad Clinical Phenotype
المؤلفون: Rhys Williams, Cinzia Sarti, Paolo Pozzilli, Mohammed I. Hawa, Alberto de Leiva, Raffaella Buzzetti, Charles Thivolet, Nanette C. Schloot, Steven J. Hunter, David R. Hadden, Sinead Brophy, Jaakko Tuomilehto, Huriya Beyan, Knud Bonnet Yderstræde, Didac Mauricio, Richard David Leslie, Guntram Schernthaner, Werner A. Scherbaum, Stavroula A Paschou, Henning Beck-Neilsen, Hubert Kolb
المصدر: Diabetes Care. 36:908-913
بيانات النشر: American Diabetes Association, 2013.
سنة النشر: 2013
مصطلحات موضوعية: Advanced and Specialized Nursing, medicine.medical_specialty, Type 1 diabetes, biology, business.industry, Cross-sectional study, Endocrinology, Diabetes and Metabolism, Insulin, medicine.medical_treatment, Glutamate decarboxylase, Autoantibody, Type 2 diabetes, medicine.disease, Diabetes mellitus, Internal medicine, Immunology, Internal Medicine, biology.protein, Medicine, Antibody, business
الوصف: OBJECTIVE Specific autoantibodies characterize type 1 diabetes in childhood but are also found in adult-onset diabetes, even when initially non–insulin requiring, e.g., with latent autoimmune diabetes (LADA). We aimed to characterize adult-onset autoimmune diabetes. RESEARCH DESIGN AND METHODS We consecutively studied 6,156 European diabetic patients attending clinics within 5 years of diagnosis (age range, 30–70 years) examined cross-sectionally clinically and for GAD antibodies (GADA) and antibodies to insulinoma-associated antigen-2 (IA-2A) and zinc-transporter 8 (ZnT8A). RESULTS Of 6,156 patients, 541 (8.8%) had GADA and only 57 (0.9%) IA-2A or ZnT8A alone. More autoantibody-positive than autoantibody-negative patients were younger, leaner, on insulin (49.5 vs. 13.2%), and female (P < 0.0001 for each), though LADA patients (9.7% of total) did not show categorically distinct clinical features from autoantibody-negative type 2 diabetes. Similarly, more GADA patients with high (>200 World Health Organization IU) (n = 403) compared with low (n = 138) titer were female, lean, and insulin treated (54.6 vs. 39.7%) (P < 0.02 for each). Autoantibody-positive patients usually had GADA (541 of 598; 90.5%) and had LADA more often than type 1 autoimmune diabetes (odds ratio 3.3). CONCLUSIONS Adult-onset autoimmune diabetes emerges as a prevalent form of autoimmune diabetes. Our results indicate that adult-onset autoimmune diabetes in Europe encompasses type 1 diabetes and LADA in the same broad clinical and autoantibody-positive spectrum. At diagnosis, patients with adult-onset autoimmune diabetes are usually non–insulin requiring and clinically indistinguishable from patients with type 2 diabetes, though they tend to be younger and leaner. Only with screening for autoantibodies, especially GADA, can they be identified with certainty.
تدمد: 1935-5548
0149-5992
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::52dcd44cc2ee0dedef423f73e422210bTest
https://doi.org/10.2337/dc12-0931Test
حقوق: OPEN
رقم الانضمام: edsair.doi...........52dcd44cc2ee0dedef423f73e422210b
قاعدة البيانات: OpenAIRE