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Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents

The type and the amount of dietary fat have a significant influence on the metabolic pathways involved in the development of obesity, metabolic syndrome, diabetes type 2 and cardiovascular diseases. However, it is unknown to what extent this modulation is achieved through DNA methylation. We assesse...

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Autores principales: Voisin, Sarah, Almén, Markus S, Moschonis, George, Chrousos, George P, Manios, Yannis, Schiöth, Helgi B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402618/
https://www.ncbi.nlm.nih.gov/pubmed/25074463
http://dx.doi.org/10.1038/ejhg.2014.139
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author Voisin, Sarah
Almén, Markus S
Moschonis, George
Chrousos, George P
Manios, Yannis
Schiöth, Helgi B
author_facet Voisin, Sarah
Almén, Markus S
Moschonis, George
Chrousos, George P
Manios, Yannis
Schiöth, Helgi B
author_sort Voisin, Sarah
collection PubMed
description The type and the amount of dietary fat have a significant influence on the metabolic pathways involved in the development of obesity, metabolic syndrome, diabetes type 2 and cardiovascular diseases. However, it is unknown to what extent this modulation is achieved through DNA methylation. We assessed the effects of cholesterol intake, the proportion of energy intake derived from fat, the ratio of polyunsaturated fatty acids (PUFA) to saturated fatty acids (SFA), the ratio of monounsaturated fatty acids (MUFA) to SFA, and the ratio of MUFA+PUFA to SFA on genome-wide DNA methylation patterns in normal-weight and obese children. We determined the genome-wide methylation profile in the blood of 69 Greek preadolescents (∼10 years old) as well as their dietary intake for two consecutive weekdays and one weekend day. The methylation levels of one CpG island shore and four sites were significantly correlated with total fat intake. The methylation levels of 2 islands, 11 island shores and 16 sites were significantly correlated with PUFA/SFA; of 9 islands, 26 island shores and 158 sites with MUFA/SFA; and of 10 islands, 40 island shores and 130 sites with (MUFA+PUFA)/SFA. We found significant gene enrichment in 34 pathways for PUFA/SFA, including the leptin pathway, and a significant enrichment in 5 pathways for (MUFA+PUFA)/SFA. Our results suggest that specific changes in DNA methylation may have an important role in the mechanisms involved in the physiological responses to different types of dietary fat.
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spelling pubmed-44026182015-05-01 Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents Voisin, Sarah Almén, Markus S Moschonis, George Chrousos, George P Manios, Yannis Schiöth, Helgi B Eur J Hum Genet Article The type and the amount of dietary fat have a significant influence on the metabolic pathways involved in the development of obesity, metabolic syndrome, diabetes type 2 and cardiovascular diseases. However, it is unknown to what extent this modulation is achieved through DNA methylation. We assessed the effects of cholesterol intake, the proportion of energy intake derived from fat, the ratio of polyunsaturated fatty acids (PUFA) to saturated fatty acids (SFA), the ratio of monounsaturated fatty acids (MUFA) to SFA, and the ratio of MUFA+PUFA to SFA on genome-wide DNA methylation patterns in normal-weight and obese children. We determined the genome-wide methylation profile in the blood of 69 Greek preadolescents (∼10 years old) as well as their dietary intake for two consecutive weekdays and one weekend day. The methylation levels of one CpG island shore and four sites were significantly correlated with total fat intake. The methylation levels of 2 islands, 11 island shores and 16 sites were significantly correlated with PUFA/SFA; of 9 islands, 26 island shores and 158 sites with MUFA/SFA; and of 10 islands, 40 island shores and 130 sites with (MUFA+PUFA)/SFA. We found significant gene enrichment in 34 pathways for PUFA/SFA, including the leptin pathway, and a significant enrichment in 5 pathways for (MUFA+PUFA)/SFA. Our results suggest that specific changes in DNA methylation may have an important role in the mechanisms involved in the physiological responses to different types of dietary fat. Nature Publishing Group 2015-05 2014-07-30 /pmc/articles/PMC4402618/ /pubmed/25074463 http://dx.doi.org/10.1038/ejhg.2014.139 Text en Copyright © 2015 Macmillan Publishers Limited http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Article
Voisin, Sarah
Almén, Markus S
Moschonis, George
Chrousos, George P
Manios, Yannis
Schiöth, Helgi B
Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents
title Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents
title_full Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents
title_fullStr Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents
title_full_unstemmed Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents
title_short Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents
title_sort dietary fat quality impacts genome-wide dna methylation patterns in a cross-sectional study of greek preadolescents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402618/
https://www.ncbi.nlm.nih.gov/pubmed/25074463
http://dx.doi.org/10.1038/ejhg.2014.139
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