We recently assessed 1st and 2nd phase ß-cell insulin secretion by applying the same model of glucose-induced insulin secretion to plasma glucose and C-peptide curves during both IVGTTs and hyperglicemic clamps. In the present study we have extended the same modeling strategy to standard OGTT (time 0’-120’). We performed in 31 subjects (18 with normal glucose regulation [NGR], 7 with impared glucose regulation [IGR], and 6 with newly diagnosed type 2 diabetes [T2DM]) a standard OGTT (blood samples for plasma glucose/C-peptide were collected every 5’-20’ from 0’ to 120’), and an IVGTT (12 g per m2 of BSA; blood samples collected every 1’-20’ from 0’ to 180’-240’) on 2 separate day. We have applied the same modeling strategy to both tests and obtained a fairly good fit of the data in both the IVGTT and the OGTT. We thus estimated first (1st) and second (2nd) phase insulin secretion during both tests. Results are normalized per m2 of BSA. In the pooled data, OGTT 1st and 2nd (2996±299 e 96.1±7.37, respectively) were significantly higher (p<0.01) than IVGTT 1st and 2nd (467±67 e 43.8±4.3), reflecting the well known potentiating effect of oral glucose on -cell response. Moreover, OGTT 1st and 2nd were positively and significantly correlated to IVGTT 1st and 2nd (r=0.50 e r=0.52, respectively; p<0.01 for both). Finally, in NGR, IGR and T2DM subjects OGTT 1st (3609±430, 2439±437 e 1807±220) and 2nd (112±9.5, 80.8±13 e 66.2± 11.5, respectively) showed a similar declining pattern as the one observed with the IVGTT (624±83, 427±112 and 42.8±27.8 for IVGTT 1st; 44.8±6.5, 48.3±9.1 and 35.5±5 for IVGTT 2nd, respectively). These data demonstrate that is feasible to assess 1st and the 2nd insulin secretion phase during a standard OGTT and provide a physiological tool to measure ß-cell function in states of normal and/or altered glucose regulation.
Assessement of 1th and snd phase of insulin secretion during OGTT and IVGTT
TROMBETTA, Maddalena;BIFARI, Francesco;BONORA, Enzo;
2004-01-01
Abstract
We recently assessed 1st and 2nd phase ß-cell insulin secretion by applying the same model of glucose-induced insulin secretion to plasma glucose and C-peptide curves during both IVGTTs and hyperglicemic clamps. In the present study we have extended the same modeling strategy to standard OGTT (time 0’-120’). We performed in 31 subjects (18 with normal glucose regulation [NGR], 7 with impared glucose regulation [IGR], and 6 with newly diagnosed type 2 diabetes [T2DM]) a standard OGTT (blood samples for plasma glucose/C-peptide were collected every 5’-20’ from 0’ to 120’), and an IVGTT (12 g per m2 of BSA; blood samples collected every 1’-20’ from 0’ to 180’-240’) on 2 separate day. We have applied the same modeling strategy to both tests and obtained a fairly good fit of the data in both the IVGTT and the OGTT. We thus estimated first (1st) and second (2nd) phase insulin secretion during both tests. Results are normalized per m2 of BSA. In the pooled data, OGTT 1st and 2nd (2996±299 e 96.1±7.37, respectively) were significantly higher (p<0.01) than IVGTT 1st and 2nd (467±67 e 43.8±4.3), reflecting the well known potentiating effect of oral glucose on -cell response. Moreover, OGTT 1st and 2nd were positively and significantly correlated to IVGTT 1st and 2nd (r=0.50 e r=0.52, respectively; p<0.01 for both). Finally, in NGR, IGR and T2DM subjects OGTT 1st (3609±430, 2439±437 e 1807±220) and 2nd (112±9.5, 80.8±13 e 66.2± 11.5, respectively) showed a similar declining pattern as the one observed with the IVGTT (624±83, 427±112 and 42.8±27.8 for IVGTT 1st; 44.8±6.5, 48.3±9.1 and 35.5±5 for IVGTT 2nd, respectively). These data demonstrate that is feasible to assess 1st and the 2nd insulin secretion phase during a standard OGTT and provide a physiological tool to measure ß-cell function in states of normal and/or altered glucose regulation.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.