B. Rakotoambinina et al., INSULIN RESPONSES TO INTRAVENOUS GLUCOSE AND THE HYPERGLYCEMIC CLAMP IN CYSTIC-FIBROSIS PATIENTS WITH DIFFERENT DEGREES OF GLUCOSE-TOLERANCE, Pediatric research, 36(5), 1994, pp. 667-671
The relationship between altered insulin secretion and impaired glucos
e tolerance was studied in 32 cystic fibrosis patients, 16 men and 16
women, aged 8-26 y, using oral and i.v. glucose tolerance tests and a
hyperglycemic glucose clamp (10 mmol/L). Seven of these subjects were
already being treated with insulin; seven had fasting blood glucose le
vels below 7.2 mmol/L but satisfied diabetic criteria at the oral gluc
ose tolerance test; glucose tolerance was impaired in 13 subjects and
normal in five. The insulin responses to the two i.v. glucose stimuli
were inversely correlated with the plasma glucose levels (60 and 120 m
in) and the area under the curve of the oral glucose tolerance test. H
owever, the acute insulin response to i.v. glucose was severely altere
d in patients with impaired glucose tolerance, whereas plasma insulin
levels during the hyperglycemic clamp did not differ from those of hea
lthy subjects. The responses to the two stimuli were dramatically low
in the diabetic patients. These results suggest that cystic fibrosis p
atients with normal or impaired glucose tolerance retain their capacit
y to secrete insulin. Alterations in the acute phase of glucose-stimul
ated insulin secretion seem to be principally responsible for the earl
y impairment in glucose tolerance.