High-dose IGF-I increased glucose disappearance more than insulin in fasted normal subjects.
In plain wordsIn fasted normal subjects, high-dose IGF-I increased glucose uptake more than insulin.
- Peptide
- IGF-1 (mecasermin)
- Outcome
- IncreaseGlucose disappearance
- Study
n: not reported in source
- Comparator
- Insulin
- Outcome group
- Glycemic control · Metabolic and weight
- Studied dose
- 30 micrograms/kg per h · infusion · 8 hAs given in this study (human).
Measurements
- Glucose rate of disappearance, increase from baseline
- 239%
- High dose IGF-I
- Glucose rate of disappearance, increase from baseline
- 197%
- High dose insulin
- Reported +/- term for Glucose rate of disappearance, increase from baseline
- 16%
- High dose IGF-I; uncertainty type not stated in the summary
- Reported +/- term for Glucose rate of disappearance, increase from baseline
- 18%
- High dose insulin; uncertainty type not stated in the summary
- P value for Glucose rate of disappearance, increase from baseline
- 0.021 dimensionless
- High dose IGF-I versus high dose insulin
Source sentences
Glucose rate of disappearance (measured by [6,6-D2]-glucose infusions) increased from baseline by 239 +/- 16% during high dose IGF-I vs 197 +/- 18% during insulin (P = 0.021 vs IGF-I).
2 context sentences(design, population, supporting numbers)
To compare the metabolic effects of elevated plasma concentrations of IGF-I and insulin, overnight-fasted normal subjects were studied twice, once receiving IGF-I and once insulin at doses that resulted in identical increases in glucose uptake during 8-h euglycemic clamping.
Recombinant human IGF-I or insulin were infused in one group at high doses (30 micrograms/kg per h IGF-I or 0.23 nmol/kg per h insulin) and in another group at low doses (5 micrograms/kg per h IGF-I or 0.04 nmol/kg per h insulin).