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Clinical and metabolic characteristics of patients with latent autoimmune diabetes in adults (LADA): absence of rapid beta-cell loss in patients with tight metabolic control.

Authors :
Chaillous L
Bouhanick B
Kerlan V
Mathieu E
Lecomte P
Ducluzeau PH
Delamaire M
Sonnet E
Maugendre D
Maréchaud R
Rohmer V
Saï P
Charbonnel B
Source :
Diabetes & metabolism [Diabetes Metab] 2010 Feb; Vol. 36 (1), pp. 64-70. Date of Electronic Publication: 2010 Jan 08.
Publication Year :
2010

Abstract

Aim and Methods: The present study compared the clinical and metabolic characteristics of latent autoimmune diabetes in adults (LADA) with type 2 diabetes, as well as the residual beta-cell function and progression to insulin treatment, over a 2-year follow-up period, of antibody (Ab)-positive and Ab-negative patients who achieved tight glycaemic control (HbA(1c) 7.0+/-0.8% and 6.5+/-0.9%, respectively, at the time of entry into the study).<br />Results: Glutamic acid decarboxylase antibodies (GADA) and/or islet cell antibodies (ICA) were detected in 10% of patients presenting with non-insulin-dependent diabetes. Around half of Ab-positive patients required insulin treatment during the follow-up. Ab-positive patients displayed lower stimulated C-peptide levels both at entry and during the follow-up compared with Ab-negative patients, although no significant decline in C-peptide levels was observed in either subgroup over two years. Nevertheless, Ab-positive patients progressed more frequently to insulin treatment, and stimulated C-peptide tended to decrease in LADA patients who subsequently required insulin, whereas it remained stable in those who were non-insulin-dependent. In those who progressed, the trend towards C-peptide decline persisted even after starting insulin treatment.<br />Conclusion: LADA patients demonstrate lower residual beta-cell function than do type 2 diabetes patients. However, those who achieve tight metabolic control do not present with a rapid decline in beta-cell function. Further studies are needed to determine the optimal treatment strategy in such patients.<br /> (Copyright (c) 2009 Elsevier Masson SAS. All rights reserved.)

Details

Language :
English
ISSN :
1878-1780
Volume :
36
Issue :
1
Database :
MEDLINE
Journal :
Diabetes & metabolism
Publication Type :
Academic Journal
Accession number :
20060765
Full Text :
https://doi.org/10.1016/j.diabet.2009.07.004