Exp Clin Endocrinol Diabetes 1990; 95(1): 123-128
DOI: 10.1055/s-0029-1210944
Original

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Autoantibodies against Insulin (IAA), C-peptide (CAA), and Glucagon (GAA) in New-Onset Type 1 Diabetic Patients*)

H. Keilacker, I. Rjasanowski, K. P. Woltanski, B. Ziegler, K. D. Kohnert, D. Michaelis, M. Ziegler
  • Central Institute of Diabetes “Gerhardt Katsch” (Director: OMR Prof. Dr. sc. med. H. Bibergeil), Karlsburg/GDR
*) Dedicated to Professor H. Bibergeil on the occasion of his 65th birthday
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Publikationsverlauf

1989

Publikationsdatum:
16. Juli 2009 (online)

Summary

Autoantibodies against insulin, C-peptide, and glucagon were determined by radio -binding assay in 63 new-onset Type 1 (insulin-dependent) diabetic patients as well as in 70 controls. Plasma peptide binding was determined by means of 125I-labeled peptides and charcoal-dextrane separation technique. Binding values exceeding the mean plus three standard deviations of the controls were considered as antibody-positive. Sixteen patients (25%) were positive for IAA, as 6 (10%) were positive for CAA and 2 (3%) for GAA. Of all control subjects, none were positive for either IAA or CAA, whereas 2 (2%) had GAA. The mean 125I-glucagon binding in the patients' group was, however, slightly enhanced and could be suppressed to normal values by excess unlabeled glucagon. The presence of IAA and/or CAA was significantly associated with more severe symptoms at diabetes manifestation. These results indicate that in new-onset Type 1 diabetics autoimmunity arises against all the insular peptides tested but is predominantly directed against those antigens secreted from the beta cells. Nevertheless, extremely low-binding GAA seem to be common in these patients. The determination of IAA/CAA might be useful in detecting a possible heterogeneity of Type 1 diabetes with regard to its clinical mode of manifestation.