Document Detail


Incretin action maintains insulin secretion, but not hepatic insulin action, in people with impaired fasting glucose.
MedLine Citation:
PMID:  20708814     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
AIMS: To determine whether altered GLP-1 activity contributes to the abnormal endogenous glucose production (EGP) and insulin secretion characteristic of people with impaired fasting glucose (IFG).
METHODS: People with IFG (n=10) and normal glucose tolerance (NGT; n=13) underwent assessment of EGP (via [6,6-(2)H(2)]-glucose infusion). Parameters of whole body insulin action and secretion were estimated by IVGTT and OGTT. Measures of EGP and insulin secretion were made before and after sitagliptin administration.
RESULTS: EGP was not different at baseline (glucose R(a); 1.47+/-0.08 vs. 1.46+/-0.05mg/kg/min, IFG vs. NGT, p=0.93). However, when differences in circulating insulin were accounted for (EGPXSSPI; 20.2+/-2.1 vs. 14.4+/-1.0AU, vs. NGT, p=0.03) the hepatic insulin resistance index was significantly higher in IFG. Baseline insulin action (S(i); 2.3+/-0.1x10(-4)/microU/ml vs. 3.5+/-0.4x10(-4)/microU/ml, p=0.01, IFG vs. NGT) and secretion (DI; 587+/-81x10(-4)/min vs. 1171+/-226x10(-4)/min, p=0.04, IFG vs. NGT) were impaired in IFG when evaluated by the IVGTT, but not by OGTT (insulin sensitivity 4.52+/-1.08x10(-4)dl/kg/min vs. 6.73+/-1.16x10(-4)dl/kg/min, IFG vs. NGT, p=0.16; indices of basal (Phi(b)), static (Phi(s)), dynamic (Phi(d)), and total (Phi(t)) insulin secretion, p>0.07). Sitagliptin did not change EGP or insulin secretion in either group.
CONCLUSIONS: Incretin action maintained insulin secretion, but not hepatic insulin action, in people with IFG.
Authors:
Leigh Perreault; Chiara Dalla Man; Devon M Hunerdosse; Claudio Cobelli; Bryan C Bergman
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Publication Detail:
Type:  Controlled Clinical Trial; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2010-08-13
Journal Detail:
Title:  Diabetes research and clinical practice     Volume:  90     ISSN:  1872-8227     ISO Abbreviation:  Diabetes Res. Clin. Pract.     Publication Date:  2010 Oct 
Date Detail:
Created Date:  2010-09-06     Completed Date:  2011-01-18     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8508335     Medline TA:  Diabetes Res Clin Pract     Country:  Ireland    
Other Details:
Languages:  eng     Pagination:  87-94     Citation Subset:  IM    
Affiliation:
University of Colorado at Denver School of Medicine, Aurora, CO 80045, USA. leigh.perreault@ucdenver.edu
Data Bank Information
Bank Name/Acc. No.:
ClinicalTrials.gov/NCT00795275
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MeSH Terms
Descriptor/Qualifier:
Aged
Blood Glucose / analysis
Body Mass Index
C-Peptide / blood
Dipeptidyl-Peptidase IV Inhibitors / adverse effects,  therapeutic use*
Female
Glucagon-Like Peptide 1 / blood,  physiology
Glucose / chemistry,  pharmacokinetics
Glucose Tolerance Test
Humans
Hyperglycemia / blood,  drug therapy*
Incretins / blood,  physiology*
Insulin / blood,  secretion*
Insulin Resistance
Insulin-Secreting Cells / drug effects*,  secretion
Liver / drug effects*,  physiopathology
Male
Middle Aged
Pyrazines / adverse effects,  therapeutic use*
Severity of Illness Index
Triazoles / adverse effects,  therapeutic use*
Grant Support
ID/Acronym/Agency:
RR-0036/RR/NCRR NIH HHS
Chemical
Reg. No./Substance:
0/Blood Glucose; 0/C-Peptide; 0/Dipeptidyl-Peptidase IV Inhibitors; 0/Incretins; 0/Pyrazines; 0/Triazoles; 0/sitagliptin; 11061-68-0/Insulin; 50-99-7/Glucose; 89750-14-1/Glucagon-Like Peptide 1

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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