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Metabolite Profiles During 0ral Glucose Challenge.

Authors :
Ho, Jennifer E.
Larson, Martin G.
Vasan, Ramachandran S.
Ghorbani, Anahita
Cheng, Susan
Rhee, Eugene P.
Florez, Jose C.
Clish, Clary B.
Gerszten, Robert E.
Wang, Thomas J.
Source :
Diabetes; Aug2013, Vol. 62 Issue 8, p2689-2698, 10p, 4 Charts, 4 Graphs
Publication Year :
2013

Abstract

To identify distinct biological pathways of glucose metabolism, we conducted a systematic evaluation of biochemical changes after an oral glucose tolerance test (OGTT in a community-based population. Metabolic profiling was performed on 377 nondiabetic Framingham Offspring cohort participants (mean age 57 years, 42%5 women BMI 30 kg/m² before and after OGTT. Changes in metabolite levels were evaluated with paired Student t tests, cluster-based analyses, and multivariable linear regression to examine differences associated with insulin resistance. Of 110 metabolites tested, 91 significantly changed with OGTT (P ≤ 0.0005 for all). Amino acid β-bydroxybutyrate, and tricarboxylic acid cycle intermediates de creased after OGTT, and glycolysis products increased, consistent with physiological insulin actions. Other pathways affected by OGTT included decreases in serotonin derivatives, urea cycle metabolites, and B vitamins. We also observed an increase in conjugated, and a decrease in unconjugated, bile acids. Changes in β-hydroxybutyrate, isoleucine, lactate, and pyridoxate were blunted in those with insulin resistance. Our findings demonstrate changes in 91 metabolites representing distinct biological pathways that are perturbed in response to an OGTT. We also identify metabolite responses that distinguish individuals with and without insulin resistance. These findings suggest that unique metabolic phenotypes can be unmasked by OGTT in the prediabetic state. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00121797
Volume :
62
Issue :
8
Database :
Complementary Index
Journal :
Diabetes
Publication Type :
Academic Journal
Accession number :
89423715
Full Text :
https://doi.org/10.2337/db12-0754