Regulation of endogenous glucose production (EGP) and insulin secretion are major actions of glucagon-like peptide-1 (GLP-1). Determining whether alterations in GLP-1 may contribute to abnormal EGP and insulin secretion in people with impaired fasting glucose (IFG) was the objective of the current study. The investigators hypothesized that defects in GLP-1 may explain the inappropriate basal EGP and diminished insulin secretion in IFG, and, furthermore, that by increasing circulating GLP-1 levels (using a new medicine called "sitagliptin") the investigators could reverse these defects.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
26
Januvia 100 mg po qd x 28 days for all subjects after baseline measures made
University of Colorado Denver
Aurora, Colorado, United States
Change in Endogenous Glucose Production
Time frame: Baseline and 28 days
Change in Insulin Secretion
Time frame: Baseline and 28 days
Insulin Secretion in Response to Oral vs. IV Glucose
Time frame: Baseline
Baseline and Change in Hormones, Substrates and Insulin Action: C-peptide
Time frame: Baseline and 28 days
Baseline and Change in Hormones, Substrates and Insulin Action: Glucagon
Time frame: Baseline and 28 days
Baseline and Change in Hormones, Substrates and Insulin Action: GLP-1
Time frame: Baseline and 28 days
Baseline and Change in Hormones, Substrates and Insulin Action: Lactate
Time frame: Baseline and 28 days
Baseline and Change in Hormones, Substrates and Insulin Action: FFA
Time frame: Baseline and 28 days
Baseline and Change in Hormones, Substrates and Insulin Action: Glycerol
Time frame: Baseline and 28 days
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