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Diabetes, Vol 29, Issue 8 589-592, Copyright © 1980 by American Diabetes Association
Islet cell and other organ-specific antibodies in U.S. Caucasians and Blacks with insulin-dependent diabetes mellitus
M Neufeld, NK Maclaren, WJ Riley, D Lezotte, JV McLaughlin, J Silverstein and AL Rosenbloom
Islet cell antibodies (ICA) were detected in 168 (33%) of 504 patients with
insulin-dependent diabetes mellitus (IDDM). Mean age of onset of IDDM was
8.6 +/- 0.2 yr and mean age at testing was 13.4 +/- 0.3 yr. None of 162
controls without diabetes (mean age 21.8 +/- 0.9 yr) had ICA. Caucasian
patients (404) had a 74% frequency of ICA within 3 mo of diagnosis and an
overall ICA frequency of 36%. These results were similar to those reported
from Europe. Black patients (100) had lower frequencies of ICA (P <
0.01) and thyroid antibodies (P < 0.05). Caucasian patients with onset
of IDDM before 5 yr of age (107) had a lower frequency (P < 0.01) of ICA
(21%) than those (297) with a later age of onset (42%). Patients with
persistent ICA beyond 5 yr of IDDM had increased frequencies of gastric
parietal and adrenal cortex cell antibodies. Thyroid microsomal antibodies
were less frequent (P < 0.05) in blacks (4%) than in Caucasians (20%).
The former did not have adrenal antibodies. Similar ICA frequencies among
Caucasians with IDDM in the U.S. and in Europe suggest that etiologic
factors are similar in the two geographic regions. The lower frequencies of
ICA in patients with IDDM onset before 5 yr of age suggest that some of
these patients may have a different etiology and/or a more rapid
disappearance of islet cell antigens than patients with a later onset.l The
lower ICA frequencies in black patients can be explained by heterogeneity
of IDDM in this group and by admixture of IDDM susceptibility genes from
the Caucasian genome to the black genome.

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Copyright © 1980 by the American Diabetes Association.
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