Patients and method: Since this has therapeutical implications, ten pa
tients were identified with new-onset type 2 diabetes, defined by fast
ing blood glucose concentrations below 120 mg/dl, no previous history
of diabetes and venous blood glucose concentrations at 120 min of an o
ral glucose tolerance test above 200 mg/dl (x 262 +/- 15 mg/dl) (''dia
betic glucose tolerance''). Ten subjects with normal glucose tolerance
and no familial history olNIDDM, who were matched for gender, age (n:
56 +/- 2 years, D: 61 +/- 5) and BMI (n: 28 +/- 1, D: 28 +/- 1), serv
ed as control group. Serum insulin was measured using a double-antibod
y sandwich-rest (no cross-reaction with proinsulin and C-peptide) at 0
, 30 and 120 min of an oGTT. Result: In the diabetic group, basal insu
lin levels were found to be elevated 1.7-fold (n: 7.9 +/- 1.4 uU/ml, D
: 13.3 +/- 1.4, p = 0.03), 30 min values were the same in both groups
and the 120 min value war 4.6-fold higher in the diabetic group (n: 33
.9 +/- 8.7, D: 156.2 +/- 27.4, p = 0.0008). Conclusion: Thus, in new-o
nset diabetes, in the early phase of an oGTT (30 min) both insulin sec
retion and action are reduced, in the second phase (120 min) severe in
sulin resistance predominates at maximally stimulated secretion. These
findings underline the therapeutical strategy in these patients, to r
educe postprandial blood glucose increments and improve insulin resist
ance by diet and, if necessary, pharmacologically.