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Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance.

Citation
Nowak, C., et al. “Glucose Challenge Metabolomics Implicates Medium-Chain Acylcarnitines In Insulin Resistance.”. Scientific Reports, p. 8691.
Center Stanford University
Author Christoph Nowak, Susanne Hetty, Samira Salihovic, Casimiro Castillejo-López, Andrea Ganna, Naomi L Cook, Corey D Broeckling, Jessica E Prenni, Xia Shen, Vilmantas Giedraitis, Johan Ärnlöv, Lars Lind, Christian Berne, Johan Sundström, Tove Fall, Erik Ingelsson
Abstract

Insulin resistance (IR) predisposes to type 2 diabetes and cardiovascular disease but its causes are incompletely understood. Metabolic challenges like the oral glucose tolerance test (OGTT) can reveal pathogenic mechanisms. We aimed to discover associations of IR with metabolite trajectories during OGTT. In 470 non-diabetic men (age 70.6 ± 0.6 years), plasma samples obtained at 0, 30 and 120 minutes during an OGTT were analyzed by untargeted liquid chromatography-mass spectrometry metabolomics. IR was assessed with the hyperinsulinemic-euglycemic clamp method. We applied age-adjusted linear regression to identify metabolites whose concentration change was related to IR. Nine trajectories, including monounsaturated fatty acids, lysophosphatidylethanolamines and a bile acid, were significantly associated with IR, with the strongest associations observed for medium-chain acylcarnitines C10 and C12, and no associations with L-carnitine or C2-, C8-, C14- or C16-carnitine. Concentrations of C10- and C12-carnitine decreased during OGTT with a blunted decline in participants with worse insulin resistance. Associations persisted after adjustment for obesity, fasting insulin and fasting glucose. In mouse 3T3-L1 adipocytes exposed to different acylcarnitines, we observed blunted insulin-stimulated glucose uptake after treatment with C10- or C12-carnitine. In conclusion, our results identify medium-chain acylcarnitines as possible contributors to IR.

Year of Publication
2018
Journal
Scientific reports
Volume
8
Issue
1
Number of Pages
8691
Date Published
12/2018
ISSN Number
2045-2322
DOI
10.1038/s41598-018-26701-0
Alternate Journal
Sci Rep
PMID
29875472
PMCID
PMC5989236
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