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Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat

BACKGROUND: Genetic factors that predict responses to diet may ultimately be used to individualize dietary recommendations. We used physiogenomics to explore associations among polymorphisms in candidate genes and changes in relative body fat (Δ%BF) to low fat and low carbohydrate diets. METHODS: We...

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Autores principales: Seip, Richard L, Volek, Jeff S, Windemuth, Andreas, Kocherla, Mohan, Fernandez, Maria Luz, Kraemer, William J, Ruaño, Gualberto
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2270845/
https://www.ncbi.nlm.nih.gov/pubmed/18254975
http://dx.doi.org/10.1186/1743-7075-5-4
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author Seip, Richard L
Volek, Jeff S
Windemuth, Andreas
Kocherla, Mohan
Fernandez, Maria Luz
Kraemer, William J
Ruaño, Gualberto
author_facet Seip, Richard L
Volek, Jeff S
Windemuth, Andreas
Kocherla, Mohan
Fernandez, Maria Luz
Kraemer, William J
Ruaño, Gualberto
author_sort Seip, Richard L
collection PubMed
description BACKGROUND: Genetic factors that predict responses to diet may ultimately be used to individualize dietary recommendations. We used physiogenomics to explore associations among polymorphisms in candidate genes and changes in relative body fat (Δ%BF) to low fat and low carbohydrate diets. METHODS: We assessed Δ%BF using dual energy X-ray absorptiometry (DXA) in 93 healthy adults who consumed a low carbohydrate diet (carbohydrate ~12% total energy) (LC diet) and in 70, a low fat diet (fat ~25% total energy) (LF diet). Fifty-three single nucleotide polymorphisms (SNPs) selected from 28 candidate genes involved in food intake, energy homeostasis, and adipocyte regulation were ranked according to probability of association with the change in %BF using multiple linear regression. RESULTS: Dieting reduced %BF by 3.0 ± 2.6% (absolute units) for LC and 1.9 ± 1.6% for LF (p < 0.01). SNPs in nine genes were significantly associated with Δ%BF, with four significant after correction for multiple statistical testing: rs322695 near the retinoic acid receptor beta (RARB) (p < 0.005), rs2838549 in the hepatic phosphofructokinase (PFKL), and rs3100722 in the histamine N-methyl transferase (HNMT) genes (both p < 0.041) due to LF; and the rs5950584 SNP in the angiotensin receptor Type II (AGTR2) gene due to LC (p < 0.021). CONCLUSION: Fat loss under LC and LF diet regimes appears to have distinct mechanisms, with PFKL and HNMT and RARB involved in fat restriction; and AGTR2 involved in carbohydrate restriction. These discoveries could provide clues to important physiologic mechanisms underlying the Δ%BF to low carbohydrate and low fat diets.
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spelling pubmed-22708452008-03-21 Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat Seip, Richard L Volek, Jeff S Windemuth, Andreas Kocherla, Mohan Fernandez, Maria Luz Kraemer, William J Ruaño, Gualberto Nutr Metab (Lond) Research BACKGROUND: Genetic factors that predict responses to diet may ultimately be used to individualize dietary recommendations. We used physiogenomics to explore associations among polymorphisms in candidate genes and changes in relative body fat (Δ%BF) to low fat and low carbohydrate diets. METHODS: We assessed Δ%BF using dual energy X-ray absorptiometry (DXA) in 93 healthy adults who consumed a low carbohydrate diet (carbohydrate ~12% total energy) (LC diet) and in 70, a low fat diet (fat ~25% total energy) (LF diet). Fifty-three single nucleotide polymorphisms (SNPs) selected from 28 candidate genes involved in food intake, energy homeostasis, and adipocyte regulation were ranked according to probability of association with the change in %BF using multiple linear regression. RESULTS: Dieting reduced %BF by 3.0 ± 2.6% (absolute units) for LC and 1.9 ± 1.6% for LF (p < 0.01). SNPs in nine genes were significantly associated with Δ%BF, with four significant after correction for multiple statistical testing: rs322695 near the retinoic acid receptor beta (RARB) (p < 0.005), rs2838549 in the hepatic phosphofructokinase (PFKL), and rs3100722 in the histamine N-methyl transferase (HNMT) genes (both p < 0.041) due to LF; and the rs5950584 SNP in the angiotensin receptor Type II (AGTR2) gene due to LC (p < 0.021). CONCLUSION: Fat loss under LC and LF diet regimes appears to have distinct mechanisms, with PFKL and HNMT and RARB involved in fat restriction; and AGTR2 involved in carbohydrate restriction. These discoveries could provide clues to important physiologic mechanisms underlying the Δ%BF to low carbohydrate and low fat diets. BioMed Central 2008-02-06 /pmc/articles/PMC2270845/ /pubmed/18254975 http://dx.doi.org/10.1186/1743-7075-5-4 Text en Copyright © 2008 Seip et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Seip, Richard L
Volek, Jeff S
Windemuth, Andreas
Kocherla, Mohan
Fernandez, Maria Luz
Kraemer, William J
Ruaño, Gualberto
Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat
title Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat
title_full Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat
title_fullStr Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat
title_full_unstemmed Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat
title_short Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat
title_sort physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2270845/
https://www.ncbi.nlm.nih.gov/pubmed/18254975
http://dx.doi.org/10.1186/1743-7075-5-4
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