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Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes

Metabolic profiling of individuals with type 2 diabetes mellitus (T2DM) has previously been limited to single-time-point samples, ignoring time-of-day variation. Here, we tested our hypothesis that body mass and T2DM affect daily rhythmicity and concentrations of circulating metabolites across a 24-...

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Autores principales: Isherwood, Cheryl M., Van der Veen, Daan R., Johnston, Jonathan D., Skene, Debra J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Federation of American Societies for Experimental Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690388/
https://www.ncbi.nlm.nih.gov/pubmed/28821636
http://dx.doi.org/10.1096/fj.201700323R
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author Isherwood, Cheryl M.
Van der Veen, Daan R.
Johnston, Jonathan D.
Skene, Debra J.
author_facet Isherwood, Cheryl M.
Van der Veen, Daan R.
Johnston, Jonathan D.
Skene, Debra J.
author_sort Isherwood, Cheryl M.
collection PubMed
description Metabolic profiling of individuals with type 2 diabetes mellitus (T2DM) has previously been limited to single-time-point samples, ignoring time-of-day variation. Here, we tested our hypothesis that body mass and T2DM affect daily rhythmicity and concentrations of circulating metabolites across a 24-h day in 3 age-matched, male groups—lean, overweight/obese (OW/OB), and OW/OB with T2DM—in controlled laboratory conditions, which were not confounded by large meals. By using targeted liquid chromatography/mass spectrometry metabolomics, we quantified 130 plasma metabolites every 2 h over 24 h, and we show that average metabolite concentrations were significantly altered by increased body mass (90 of 130) and T2DM (56 of 130). Thirty-eight percent of metabolites exhibited daily rhythms in at least 1 study group, and where a metabolite was rhythmic in >1 group, its peak time was comparable. The optimal time of day was assessed to provide discriminating biomarkers. This differed between metabolite classes and study groups—for example, phospholipids showed maximal difference at 5:00 AM (lean vs. OW/OB) and at 5:00 PM (OW/OB vs. T2DM). Metabolites that were identified with both robust 24-h rhythms and significant concentration differences between study groups emphasize the importance of controlling the time of day for diagnosis and biomarker discovery, offering a significant improvement over current single sampling.—Isherwood, C. M., Van der Veen, D. R., Johnston, J. D., Skene, D. J. Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes.
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spelling pubmed-56903882017-11-22 Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes Isherwood, Cheryl M. Van der Veen, Daan R. Johnston, Jonathan D. Skene, Debra J. FASEB J Research Metabolic profiling of individuals with type 2 diabetes mellitus (T2DM) has previously been limited to single-time-point samples, ignoring time-of-day variation. Here, we tested our hypothesis that body mass and T2DM affect daily rhythmicity and concentrations of circulating metabolites across a 24-h day in 3 age-matched, male groups—lean, overweight/obese (OW/OB), and OW/OB with T2DM—in controlled laboratory conditions, which were not confounded by large meals. By using targeted liquid chromatography/mass spectrometry metabolomics, we quantified 130 plasma metabolites every 2 h over 24 h, and we show that average metabolite concentrations were significantly altered by increased body mass (90 of 130) and T2DM (56 of 130). Thirty-eight percent of metabolites exhibited daily rhythms in at least 1 study group, and where a metabolite was rhythmic in >1 group, its peak time was comparable. The optimal time of day was assessed to provide discriminating biomarkers. This differed between metabolite classes and study groups—for example, phospholipids showed maximal difference at 5:00 AM (lean vs. OW/OB) and at 5:00 PM (OW/OB vs. T2DM). Metabolites that were identified with both robust 24-h rhythms and significant concentration differences between study groups emphasize the importance of controlling the time of day for diagnosis and biomarker discovery, offering a significant improvement over current single sampling.—Isherwood, C. M., Van der Veen, D. R., Johnston, J. D., Skene, D. J. Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes. Federation of American Societies for Experimental Biology 2017-12 2017-08-18 /pmc/articles/PMC5690388/ /pubmed/28821636 http://dx.doi.org/10.1096/fj.201700323R Text en © The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Isherwood, Cheryl M.
Van der Veen, Daan R.
Johnston, Jonathan D.
Skene, Debra J.
Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes
title Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes
title_full Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes
title_fullStr Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes
title_full_unstemmed Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes
title_short Twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes
title_sort twenty-four-hour rhythmicity of circulating metabolites: effect of body mass and type 2 diabetes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690388/
https://www.ncbi.nlm.nih.gov/pubmed/28821636
http://dx.doi.org/10.1096/fj.201700323R
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