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

Author:

Hawa Mohammed I.1,Kolb Hubert2,Schloot Nanette2,Beyan Huriya1,Paschou Stavroula A.1,Buzzetti Raffaella3,Mauricio Didac4,De Leiva Alberto4,Yderstraede Knud5,Beck-Neilsen Henning5,Tuomilehto Jaakko6,Sarti Cinzia6,Thivolet Charles7,Hadden David8,Hunter Steven8,Schernthaner Guntram9,Scherbaum Werner A.2,Williams Rhys10,Brophy Sinead10,Pozzilli Paolo111,Leslie Richard David1,

Affiliation:

1. Blizard Institute, Queen Mary University of London, London, U.K.

2. Heinrich-Heine University Düsseldorf, Düsseldorf, Germany

3. University “La Sapienza,” Rome, Italy

4. Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; Centro de Investigación Biomédica en Red en Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN)

5. Odense University Hospital, Odense, Denmark

6. National Institute for Health and Welfare, Helsinki, Finland the

7. Hospital Edouard Herriot, Lyon, France

8. Royal Victoria Hospital, Belfast, U.K. the

9. Rudolfstiftung Hospital, Vienna, Austria

10. Swansea University, Swansea, U.K.

11. University Campus Bio-Medico, Rome, Italy

Abstract

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.

Publisher

American Diabetes Association

Subject

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

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