Glutamic Acid Decarboxylase (GAD65) Autoantibodies in Prediction of  -Cell Function and Remission in Recent-Onset IDDM After Cyclosporin Treatment

Diabetes ◽  
1994 ◽  
Vol 43 (11) ◽  
pp. 1291-1296 ◽  
Author(s):  
J. S. Petersen ◽  
T. Dyrberg ◽  
A. E. Karlsen ◽  
J. Molvig ◽  
B. Michelsen ◽  
...  
Diabetologia ◽  
1996 ◽  
Vol 39 (9) ◽  
pp. 1091-1098 ◽  
Author(s):  
A. Falorni ◽  
M. Ackefors ◽  
C. Carlberg ◽  
T. Daniels ◽  
B. Persson ◽  
...  

Diabetes ◽  
2014 ◽  
Vol 63 (8) ◽  
pp. 2876-2887 ◽  
Author(s):  
S. Robert ◽  
C. Gysemans ◽  
T. Takiishi ◽  
H. Korf ◽  
I. Spagnuolo ◽  
...  

The Lancet ◽  
2011 ◽  
Vol 378 (9788) ◽  
pp. 319-327 ◽  
Author(s):  
Diane K Wherrett ◽  
Brian Bundy ◽  
Dorothy J Becker ◽  
Linda A DiMeglio ◽  
Stephen E Gitelman ◽  
...  

1997 ◽  
Vol 43 (5) ◽  
pp. 779-785 ◽  
Author(s):  
Henrik Borg ◽  
Per Fernlund ◽  
Göran Sundkvist

Abstract Recently, 65-kDa glutamic acid decarboxylase (GAD 65) antibodies (GADA) have been introduced as autoimmune markers in blood to confirm the diagnosis of insulin-dependent diabetes mellitus (IDDM). In this study, to evaluate two new assays that use 125I-labeled GAD 65, we assayed samples from 100 children with recent onset of diabetes and 100 control children; the results were compared with those of a [35S]GADA assay and with results for islet cell antibodies (ICA), the conventional autoimmune marker. Receiver operating characteristic (ROC) curve analysis showed one of the new assays (from RSR) to be more sensitive (P = 0.01) than the comparison ([35S]GADA) assay, whereas the second new assay (from Elias) was less sensitive (P <0.001). The GADA frequency at 97.5% specificity was greatest in the comparison assay: 63 of 100 vs 41 of 100 (P < 0.01) and 53 of 100 (P = 0.16) in the RSR and Elias assays, respectively. Almost all GADA-positive patients had ICA, but one-third of the ICA-positive patients was GADA-negative. Accordingly, adding GADA analysis results to ICA testing increased the frequency of detection of autoimmune markers only slightly (from 81% to 85%). In conclusion, at 97.5% specificity the [35S]GADA assay seemed to be more efficient than the 125I assays, although the difference was significant only for the Elias 125I assay. Antigen-specific antibodies other than GADA may explain the difference in GADA and ICA frequencies.


2005 ◽  
Vol 153 (6) ◽  
pp. 901-906 ◽  
Author(s):  
Matti S Ronkainen ◽  
Taina Härkönen ◽  
Jaakko Perheentupa ◽  
Mikael Knip

Objective: A humoral autoimmune response to glutamic acid decarboxylase (GAD65) is common both in patients with type 1 diabetes and in those with the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) syndrome, while overt type 1 diabetes is relatively rarely diagnosed in APECED patients. The aim of this study was to assess whether this difference in the incidence of type 1 diabetes is associated with variability in the humoral immune response to GAD65, one of the major autoantigens in type 1 diabetes. Methods: Epitope- and isotype-specific GAD65 autoantibodies were analysed in 20 patients with APECED and 20 patients with newly diagnosed type 1 diabetes alone by radiobinding assays. Results: GAD65 autoantibodies targeted the middle and carboxy-terminal regions of GAD65 and occasionally the amino-terminal region in the APECED patients and comprised mainly the IgG1 subclass and less frequently the IgG2 and IgG4 subclasses. The profile of epitope- and isotype-specific GAD65 autoantibodies was similar in type 1 diabetes and APECED, except that IgG2 subclass antibodies were observed more often and at higher levels in the patients with type 1 diabetes alone (P < 0.05). None of the measured parameters separated APECED patients with type 1 diabetes from those without type 1 diabetes. Conclusion: APECED-associated humoral autoimmunity to GAD65 does not differ markedly from that observed in type 1 diabetes; only IgG2-GAD65 antibodies may be more closely associated with the latter entity.


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