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1 IVGTT-derived insulin sensitivity was reduced by (means
3 tion (rate of glucose uptake [Rd]) during an IVGTT is more similar to the dynamics of the interstitia
4 perfectly normal glucose disposal during an IVGTT with no differences when compared with nondiabetic
6 ynamic responses of glucose or insulin to an IVGTT is an important risk factor for type 2 diabetes.
8 etes during the trial returned for OGTTs and IVGTTs 8 months after study medications were stopped.
11 t reduction in the total insulin area during IVGTTs, which was highly significant (P < 0.001), and wi
14 initial values of S(I) and S(G) derived from IVGTT's performed at study entry, there was a 10- to 20-
15 After baseline oral (OGTT) and intravenous (IVGTT) glucose tolerance testing, subjects were assigned
16 SI, calculated by minimal model analysis of IVGTT results, changed by only 4 +/- 14% during 12 weeks
19 d intravenous glucose tolerance tests (OGTT; IVGTT), hyperinsulinemic-euglycemic clamps, and measurem
23 al insulin levels were matched in the paired IVGTTs by adjusting the portal insulin dose in proportio
24 ors of postpartum IGT were a low first-phase IVGTT insulin response (P = 0.0001), a diagnosis of GDM
26 EHC), by intravenous glucose tolerance test (IVGTT) and by oral glucose tolerance test (OGTT) in 3 di
28 from an intravenous glucose tolerance test (IVGTT) and hyperglycemic clamp (HGC) in 17 nondiabetic s
33 (I.V.) glucose (I.V. glucose tolerance test [IVGTT]), arginine and glucose-potentiated arginine (gluc
35 during intravenous glucose tolerance tests (IVGTT) remains critical for stringent evaluation of nove
37 mulated intravenous glucose tolerance tests (IVGTTs) in anesthetized dogs to test the following hypot
38 Ts) and intravenous glucose tolerance tests (IVGTTs) were performed at 15-month intervals for up to 5
40 odified intravenous glucose tolerance tests (IVGTTs) were performed in dogs in which insulin was admi
42 on [via intravenous-glucose-tolerance tests (IVGTTs)].Fifty-four participants completed the study [35
43 on was restored in type 2 diabetic after the IVGTT (Phi1 x 10: 104 +/- 54 vs 228 +/- 88; P < 0.05, pr
45 was correlated with S(i) estimated from the IVGTT and the HGC (r = 0.59 and 0.76, respectively; P <
46 icularly within the first few minutes of the IVGTT, with a significantly lower area under the excursi
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