Metabolite Profiles During Oral Glucose Challenge

Author:

Ho Jennifer E.12,Larson Martin G.13,Vasan Ramachandran S.14,Ghorbani Anahita5,Cheng Susan16,Rhee Eugene P.789,Florez Jose C.101112,Clish Clary B.9,Gerszten Robert E.579,Wang Thomas J.157

Affiliation:

1. Framingham Heart Study of the National Heart, Lung, and Blood Institute and Boston University School of Medicine, Framingham, Massachusetts

2. Cardiovascular Medicine Section, Department of Medicine, Boston University Medical Center, Boston, Massachusetts

3. Department of Mathematics and Statistics, Boston University, Boston, Massachusetts

4. Division of Cardiology and Preventive Medicine, Department of Medicine, Boston University, Boston, Massachusetts

5. Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts

6. Division of Cardiology, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts

7. Cardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts

8. Renal Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts

9. Broad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts

10. Center for Human Genetic Research and Diabetes Research Center (Diabetes Unit), Massachusetts General Hospital, Boston, Massachusetts

11. Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts

12. Department of Medicine, Harvard Medical School, Boston, Massachusetts.

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% 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 acids, β-hydroxybutyrate, and tricarboxylic acid cycle intermediates decreased 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.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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