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Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation

Both gut microbiota and diet have been shown to impact visceral fat mass (VFM), a major risk factor for cardiometabolic disease, but their relative contribution has not been well characterised. We aimed to estimate and separate the effect of gut microbiota composition from that of nutrient intake on...

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Autores principales: Le Roy, Caroline I., Bowyer, Ruth C. E., Castillo-Fernandez, Juan E., Pallister, Tess, Menni, Cristina, Steves, Claire J., Berry, Sarah E., Spector, Tim D., Bell, Jordana T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611773/
https://www.ncbi.nlm.nih.gov/pubmed/31278309
http://dx.doi.org/10.1038/s41598-019-46193-w
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author Le Roy, Caroline I.
Bowyer, Ruth C. E.
Castillo-Fernandez, Juan E.
Pallister, Tess
Menni, Cristina
Steves, Claire J.
Berry, Sarah E.
Spector, Tim D.
Bell, Jordana T.
author_facet Le Roy, Caroline I.
Bowyer, Ruth C. E.
Castillo-Fernandez, Juan E.
Pallister, Tess
Menni, Cristina
Steves, Claire J.
Berry, Sarah E.
Spector, Tim D.
Bell, Jordana T.
author_sort Le Roy, Caroline I.
collection PubMed
description Both gut microbiota and diet have been shown to impact visceral fat mass (VFM), a major risk factor for cardiometabolic disease, but their relative contribution has not been well characterised. We aimed to estimate and separate the effect of gut microbiota composition from that of nutrient intake on VFM in 1760 older female twins. Through pairwise association analyses, we identified 93 operational taxonomic units (OTUs) and 10 nutrients independently linked to VFM (FDR < 5%). Conditional analyses revealed that the majority (87%) of the 93 VFM-associated OTUs remained significantly associated with VFM irrespective of nutrient intake correction. In contrast, we observed that the effect of fibre, magnesium, biotin and vitamin E on VFM was partially mediated by OTUs. Moreover, we estimated that OTUs were more accurate predictors of VFM than nutrients and accounted for a larger percentage of its variance. Our results suggest that while the role of certain nutrients on VFM appears to depend on gut microbiota composition, specific gut microbes may affect host adiposity regardless of dietary intake. The findings imply that the gut microbiota may have a greater contribution towards shaping host VFM than diet alone. Thus, microbial-based therapy should be prioritised for VFM reduction in overweight and obese subjects.
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spelling pubmed-66117732019-07-15 Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation Le Roy, Caroline I. Bowyer, Ruth C. E. Castillo-Fernandez, Juan E. Pallister, Tess Menni, Cristina Steves, Claire J. Berry, Sarah E. Spector, Tim D. Bell, Jordana T. Sci Rep Article Both gut microbiota and diet have been shown to impact visceral fat mass (VFM), a major risk factor for cardiometabolic disease, but their relative contribution has not been well characterised. We aimed to estimate and separate the effect of gut microbiota composition from that of nutrient intake on VFM in 1760 older female twins. Through pairwise association analyses, we identified 93 operational taxonomic units (OTUs) and 10 nutrients independently linked to VFM (FDR < 5%). Conditional analyses revealed that the majority (87%) of the 93 VFM-associated OTUs remained significantly associated with VFM irrespective of nutrient intake correction. In contrast, we observed that the effect of fibre, magnesium, biotin and vitamin E on VFM was partially mediated by OTUs. Moreover, we estimated that OTUs were more accurate predictors of VFM than nutrients and accounted for a larger percentage of its variance. Our results suggest that while the role of certain nutrients on VFM appears to depend on gut microbiota composition, specific gut microbes may affect host adiposity regardless of dietary intake. The findings imply that the gut microbiota may have a greater contribution towards shaping host VFM than diet alone. Thus, microbial-based therapy should be prioritised for VFM reduction in overweight and obese subjects. Nature Publishing Group UK 2019-07-05 /pmc/articles/PMC6611773/ /pubmed/31278309 http://dx.doi.org/10.1038/s41598-019-46193-w Text en © The Author(s) 2019 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
Le Roy, Caroline I.
Bowyer, Ruth C. E.
Castillo-Fernandez, Juan E.
Pallister, Tess
Menni, Cristina
Steves, Claire J.
Berry, Sarah E.
Spector, Tim D.
Bell, Jordana T.
Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation
title Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation
title_full Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation
title_fullStr Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation
title_full_unstemmed Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation
title_short Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation
title_sort dissecting the role of the gut microbiota and diet on visceral fat mass accumulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611773/
https://www.ncbi.nlm.nih.gov/pubmed/31278309
http://dx.doi.org/10.1038/s41598-019-46193-w
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