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Wiley InterScience | |||||||||
![]() Diabetic MedicineVolume 25 Issue 2, Pages 117 - 125 Published Online: 19 Nov 2007 Journal compilation © 2010 Diabetes UK
Abstract | References | Full Text: HTML, PDF (Size: 489K) | Related Articles | Citation Tracking Review Article The islet autoantibody titres: their clinical relevance in latent autoimmune diabetes in adults (LADA) and the classification of diabetes mellitus Copyright Journal compilation © 2007 Blackwell Publishing Ltd. KEYWORDS glutamic acid decarboxylase • islet cell cytoplasmic autoantibodies • latent autoimmune diabetes in adults • Type 1 diabetes • Type 2 diabetes Diabet. Med. 25, 117–125 (2008) ABSTRACT
Latent autoimmune diabetes in the adult (LADA) is a slowly progressive form of autoimmune diabetes, characterized by diabetes-associated autoantibody positivity. A recent hypothesis proposes that LADA consists of a heterogeneous population, wherein several subgroups can be identified based on their autoimmune status. A systematic review of the literature was carried out to appraise whether the clinical characteristics of LADA patients correlate with the titre and numbers of diabetes-associated autoantibodies. We found that the simultaneous presence of multiple autoantibodies and/or a high-titre anti-glutamic acid decarboxylase (GAD)—compared with single and low-titre autoantibody—is associated with an early age of onset, low fasting C-peptide values as a marker of reduced pancreatic B-cell function, a high predictive value for future insulin requirement, the presence of other autoimmune disorders, a low prevalence of markers of the metabolic syndrome including high body mass index, hypertension and dyslipidaemia, and a high prevalence of the genotype known to increase the risk of Type 1 diabetes. We propose a more continuous classification of diabetes mellitus, based on the finding that the clinical characteristics gradually change from classic Type 1 diabetes to LADA and finally to Type 2 diabetes. Future studies should focus on determining optimal cut-off points of anti-GAD for differentiating clinically relevant diabetes mellitus subgroups. Accepted 16 June 2007 |