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Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance
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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989236/ https://www.ncbi.nlm.nih.gov/pubmed/29875472 http://dx.doi.org/10.1038/s41598-018-26701-0 |
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author | Nowak, Christoph Hetty, Susanne Salihovic, Samira Castillejo-Lopez, Casimiro Ganna, Andrea Cook, Naomi L. Broeckling, Corey D. Prenni, Jessica E. Shen, Xia Giedraitis, Vilmantas Ärnlöv, Johan Lind, Lars Berne, Christian Sundström, Johan Fall, Tove Ingelsson, Erik |
author_facet | Nowak, Christoph Hetty, Susanne Salihovic, Samira Castillejo-Lopez, Casimiro Ganna, Andrea Cook, Naomi L. Broeckling, Corey D. Prenni, Jessica E. Shen, Xia Giedraitis, Vilmantas Ärnlöv, Johan Lind, Lars Berne, Christian Sundström, Johan Fall, Tove Ingelsson, Erik |
author_sort | Nowak, Christoph |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5989236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59892362018-06-20 Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance Nowak, Christoph Hetty, Susanne Salihovic, Samira Castillejo-Lopez, Casimiro Ganna, Andrea Cook, Naomi L. Broeckling, Corey D. Prenni, Jessica E. Shen, Xia Giedraitis, Vilmantas Ärnlöv, Johan Lind, Lars Berne, Christian Sundström, Johan Fall, Tove Ingelsson, Erik Sci Rep Article 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. Nature Publishing Group UK 2018-06-06 /pmc/articles/PMC5989236/ /pubmed/29875472 http://dx.doi.org/10.1038/s41598-018-26701-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nowak, Christoph Hetty, Susanne Salihovic, Samira Castillejo-Lopez, Casimiro Ganna, Andrea Cook, Naomi L. Broeckling, Corey D. Prenni, Jessica E. Shen, Xia Giedraitis, Vilmantas Ärnlöv, Johan Lind, Lars Berne, Christian Sundström, Johan Fall, Tove Ingelsson, Erik Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance |
title | Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance |
title_full | Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance |
title_fullStr | Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance |
title_full_unstemmed | Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance |
title_short | Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance |
title_sort | glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989236/ https://www.ncbi.nlm.nih.gov/pubmed/29875472 http://dx.doi.org/10.1038/s41598-018-26701-0 |
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