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Diabetes, Vol 37, Issue 1 81-88, Copyright © 1988 by American Diabetes Association
Correlation between minimal secretory capacity of pancreatic beta-cells and stability of diabetic control
M Fukuda, A Tanaka, Y Tahara, H Ikegami, Y Yamamoto, Y Kumahara and K Shima
Department of Medicine and Geriatrics, Osaka University Medical School, Japan.
The significance of the minimal secretory capacity of pancreatic beta-cells
for the stability of the plasma glucose level was studied in 20 patients
with insulin-dependent diabetes mellitus. Changes in plasma concentrations
of major counterregulatory hormones in response to hypoglycemia were also
investigated in these patients to clarify their contribution to diabetic
brittleness. beta-Cell function was evaluated on the basis of elevation of
plasma C-peptide immunoreactivity (CPR) during the intravenous glucagon
test with a highly sensitive assay for plasma CPR that could detect as
little as 0.03 ng/ml. After stimulation with glucagon, a significant
increase in plasma CPR was observed in 10 of the patients whose beta-cell
function had been evaluated as completely depleted by a conventional assay
for plasma CPR. A clear inverse correlation was found between the secretory
capacity of pancreatic beta-cells measured in this way and the degree of
glycemic instability (r = -.74, P less than .01). Infusion of insulin at a
rate of 0.15 U.kg-1.h-1 for 60 min caused a continuous decrease in the
plasma glucose level, resulting in neuroglycopenia in 7 of the 10 CPR
nonresponders but only 2 of the CPR responders. During insulin-induced
hypoglycemia, plasma glucagon immunoreactivity did not increase in the CPR
nonresponders but increased significantly in the CPR responders. A positive
correlation was found between the minimal residual beta-cell capacity and
the responsiveness of alpha-cells to hypoglycemia (r = .65, P less than
.01).(ABSTRACT TRUNCATED AT 250 WORDS)

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Copyright © 1988 by the American Diabetes Association.
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