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CLINICAL REVIEW |
Institute of Cell and Molecular Science (R.D.G.L., P.P.), Queen Mary College, University of London, London E1 4NS, United Kingdom; University of Wales School of Medicine (R.W.), Swansea SA2 8PP, United Kingdom; and Department of Endocrinology and Diabetes (P.P.), University Campus Bio-Medico, 83-00155 Rome, Italy
Address all correspondence and requests for reprints to: Professor David Leslie, Department of Diabetes, St. Bartholomews Hospital, West Smithfield, London EC1A 7BE, United Kingdom. E-mail: r.d.g.leslie{at}qmul.ac.uk.
Context: The aim of this review was to explore the pathogenic and clinical spectrum of type 1 diabetes, which includes a form of adult onset autoimmune diabetes usually referred to as latent autoimmune diabetes in adults (LADA). We looked at this entire range of forms of autoimmune diabetes as a spectrum of genetic and nongenetic environmental influences, diabetes-associated immune responses, and metabolic changes.
Evidence Acquisition: We assessed epidemiological, genetic, immunological, and clinical data from major articles on autoimmune diabetes, including LADA and type 1 diabetes, published since 1992.
Evidence Synthesis: Data analysis of autoimmune diabetes indi-cates that type 1 diabetes and LADA occupy different poles of the same spectrum.
Conclusion: Evidence is presented that LADA represents one end of a rainbow encompassing type 1 diabetes. The clinical nature and management of autoimmune diabetes poses important therapeutic questions regarding conventional therapy for hyperglycemia as well as therapy aiming to protect residual ß-cell function. Limiting loss of endogenous insulin secretion using immunomodulation could be valuable, not only for LADA but also for type 1 diabetes.
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