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Circulating Metabolites Associated with Body Fat and Lean Mass in Adults with Overweight/Obesity

The interplay between fat mass and lean mass within human metabolism is not completely understood. We aimed to identify specific circulating metabolomic profiles associated with these body composition compartments. Cross-sectional analyses were conducted over 236 adults with overweight/obesity from...

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Autores principales: Papandreou, Christopher, García-Gavilán, Jesús, Camacho-Barcia, Lucía, Hansen, Thea T., Sjödin, Anders, Harrold, Joanne A., Halford, Jason C. G., Bulló, Mònica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153621/
https://www.ncbi.nlm.nih.gov/pubmed/34068443
http://dx.doi.org/10.3390/metabo11050317
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author Papandreou, Christopher
García-Gavilán, Jesús
Camacho-Barcia, Lucía
Hansen, Thea T.
Sjödin, Anders
Harrold, Joanne A.
Halford, Jason C. G.
Bulló, Mònica
author_facet Papandreou, Christopher
García-Gavilán, Jesús
Camacho-Barcia, Lucía
Hansen, Thea T.
Sjödin, Anders
Harrold, Joanne A.
Halford, Jason C. G.
Bulló, Mònica
author_sort Papandreou, Christopher
collection PubMed
description The interplay between fat mass and lean mass within human metabolism is not completely understood. We aimed to identify specific circulating metabolomic profiles associated with these body composition compartments. Cross-sectional analyses were conducted over 236 adults with overweight/obesity from the Satiety Innovation (SATIN) study. Body composition was assessed by dual-energy X-ray absorptiometry. A targeted multiplatform metabolite profiling approach was applied. Associations between 168 circulating metabolites and the body composition measures were assessed using elastic net regression analyses. The accuracy of the multimetabolite weighted models was evaluated using a 10-fold cross-validation approach and the Pearson’s correlation coefficients between metabolomic profiles and body compartments were estimated. Two different profiles including 86 and 65 metabolites were selected for % body fat and lean mass. These metabolites mainly consisted of lipids (sphingomyelins, phosphatidylcholines, lysophosphatidylcholines), acylcarnitines, and amino acids. Several metabolites overlapped between these body composition measures but none of them towards the same direction. The Pearson correlation coefficients between the metabolomic profiles and % body fat or lean mass were 0.80 and 0.79, respectively. Our findings suggest alterations in lipid metabolism, fatty acid oxidation, and protein degradation with increased adiposity and decreased lean body mass. These findings could help us to better understand the interplay between body composition compartments with human metabolic processes.
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spelling pubmed-81536212021-05-27 Circulating Metabolites Associated with Body Fat and Lean Mass in Adults with Overweight/Obesity Papandreou, Christopher García-Gavilán, Jesús Camacho-Barcia, Lucía Hansen, Thea T. Sjödin, Anders Harrold, Joanne A. Halford, Jason C. G. Bulló, Mònica Metabolites Article The interplay between fat mass and lean mass within human metabolism is not completely understood. We aimed to identify specific circulating metabolomic profiles associated with these body composition compartments. Cross-sectional analyses were conducted over 236 adults with overweight/obesity from the Satiety Innovation (SATIN) study. Body composition was assessed by dual-energy X-ray absorptiometry. A targeted multiplatform metabolite profiling approach was applied. Associations between 168 circulating metabolites and the body composition measures were assessed using elastic net regression analyses. The accuracy of the multimetabolite weighted models was evaluated using a 10-fold cross-validation approach and the Pearson’s correlation coefficients between metabolomic profiles and body compartments were estimated. Two different profiles including 86 and 65 metabolites were selected for % body fat and lean mass. These metabolites mainly consisted of lipids (sphingomyelins, phosphatidylcholines, lysophosphatidylcholines), acylcarnitines, and amino acids. Several metabolites overlapped between these body composition measures but none of them towards the same direction. The Pearson correlation coefficients between the metabolomic profiles and % body fat or lean mass were 0.80 and 0.79, respectively. Our findings suggest alterations in lipid metabolism, fatty acid oxidation, and protein degradation with increased adiposity and decreased lean body mass. These findings could help us to better understand the interplay between body composition compartments with human metabolic processes. MDPI 2021-05-13 /pmc/articles/PMC8153621/ /pubmed/34068443 http://dx.doi.org/10.3390/metabo11050317 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Papandreou, Christopher
García-Gavilán, Jesús
Camacho-Barcia, Lucía
Hansen, Thea T.
Sjödin, Anders
Harrold, Joanne A.
Halford, Jason C. G.
Bulló, Mònica
Circulating Metabolites Associated with Body Fat and Lean Mass in Adults with Overweight/Obesity
title Circulating Metabolites Associated with Body Fat and Lean Mass in Adults with Overweight/Obesity
title_full Circulating Metabolites Associated with Body Fat and Lean Mass in Adults with Overweight/Obesity
title_fullStr Circulating Metabolites Associated with Body Fat and Lean Mass in Adults with Overweight/Obesity
title_full_unstemmed Circulating Metabolites Associated with Body Fat and Lean Mass in Adults with Overweight/Obesity
title_short Circulating Metabolites Associated with Body Fat and Lean Mass in Adults with Overweight/Obesity
title_sort circulating metabolites associated with body fat and lean mass in adults with overweight/obesity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153621/
https://www.ncbi.nlm.nih.gov/pubmed/34068443
http://dx.doi.org/10.3390/metabo11050317
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