Latent Autoimmune Diabetes in Adults
Definition, Prevalence, β-Cell Function, and Treatment
- 1Department of Medicine, Kungsbacka Hospital, Kungsbacka, Göteborg University, Göteborg, Sweden
- 2Division of Vascular Diseases, Department of Clinical Sciences Malmö, Lund University, Malmö University Hospital, Malmö, Sweden
- 3Division of Diabetes Epidemiology and Neuropathy, Department of Clinical Sciences Malmö, Lund University, Malmö University Hospital, Malmö, Sweden
- Address correspondence and reprint requests to Professor Göran Sundkvist, MD, PhD, Department of Endocrinology, Malmö University Hospital, SE 20 501, Malmö, Sweden. E-mail: goran.sundkvist{at}med.lu.se
Abstract
Latent autoimmune diabetes in adults (LADA) is a disorder in which, despite the presence of islet antibodies at diagnosis of diabetes, the progression of autoimmune β-cell failure is slow. LADA patients are therefore not insulin requiring, at least during the first 6 months after diagnosis of diabetes. Among patients with phenotypic type 2 diabetes, LADA occurs in 10% of individuals older than 35 years and in 25% below that age. Prospective studies of β-cell function show that LADA patients with multiple islet antibodies develop β-cell failure within 5 years, whereas those with only GAD antibodies (GADAs) or only islet cell antibodies (ICAs) mostly develop β-cell failure after 5 years. Even though it may take up to 12 years until β-cell failure occurs in some patients, impairments in the β-cell response to intravenous glucose and glucagon can be detected at diagnosis of diabetes. Consequently, LADA is not a latent disease; therefore, autoimmune diabetes in adults with slowly progressive β-cell failure might be a more adequate concept. In agreement with proved impaired β-cell function at diagnosis of diabetes, insulin is the treatment of choice.
- ADA, autoimmune diabetes in adults
- GADA, GAD antibody
- IA-2A
- IA-2 antibody
- ICA, islet cell antibody
- LADA, latent autoimmune diabetes in adults
Footnotes
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This article is based on a presentation at a symposium. The symposium and the publication of this article were made possible by an unrestricted educational grant from Servier.
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- Accepted May 23, 2005.
- Received March 1, 2005.
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