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Allelic Variants of Melanocortin 3 Receptor Gene (MC3R) and Weight Loss in Obesity: A Randomised Trial of Hypo-Energetic High- versus Low-Fat Diets

INTRODUCTION: The melanocortin system plays an important role in energy homeostasis. Mice genetically deficient in the melanocortin-3 receptor gene have a normal body weight with increased body fat, mild hypophagia compared to wild-type mice. In humans, Thr6Lys and Val81Ile variants of the melanocor...

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Autores principales: Santos, José L., De la Cruz, Rolando, Holst, Claus, Grau, Katrine, Naranjo, Carolina, Maiz, Alberto, Astrup, Arne, Saris, Wim H. M., MacDonald, Ian, Oppert, Jean-Michel, Hansen, Torben, Pedersen, Oluf, Sorensen, Thorkild I. A., Martinez, J. Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114803/
https://www.ncbi.nlm.nih.gov/pubmed/21695122
http://dx.doi.org/10.1371/journal.pone.0019934
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author Santos, José L.
De la Cruz, Rolando
Holst, Claus
Grau, Katrine
Naranjo, Carolina
Maiz, Alberto
Astrup, Arne
Saris, Wim H. M.
MacDonald, Ian
Oppert, Jean-Michel
Hansen, Torben
Pedersen, Oluf
Sorensen, Thorkild I. A.
Martinez, J. Alfredo
author_facet Santos, José L.
De la Cruz, Rolando
Holst, Claus
Grau, Katrine
Naranjo, Carolina
Maiz, Alberto
Astrup, Arne
Saris, Wim H. M.
MacDonald, Ian
Oppert, Jean-Michel
Hansen, Torben
Pedersen, Oluf
Sorensen, Thorkild I. A.
Martinez, J. Alfredo
author_sort Santos, José L.
collection PubMed
description INTRODUCTION: The melanocortin system plays an important role in energy homeostasis. Mice genetically deficient in the melanocortin-3 receptor gene have a normal body weight with increased body fat, mild hypophagia compared to wild-type mice. In humans, Thr6Lys and Val81Ile variants of the melanocortin-3 receptor gene (MC3R) have been associated with childhood obesity, higher BMI Z-score and elevated body fat percentage compared to non-carriers. The aim of this study is to assess the association in adults between allelic variants of MC3R with weight loss induced by energy-restricted diets. SUBJECTS AND METHODS: This research is based on the NUGENOB study, a trial conducted to assess weight loss during a 10-week dietary intervention involving two different hypo-energetic (high-fat and low-fat) diets. A total of 760 obese patients were genotyped for 10 single nucleotide polymorphisms covering the single exon of MC3R gene and its flanking regions, including the missense variants Thr6Lys and Val81Ile. Linear mixed models and haplotype-based analysis were carried out to assess the potential association between genetic polymorphisms and differential weight loss, fat mass loss, waist change and resting energy expenditure changes. RESULTS: No differences in drop-out rate were found by MC3R genotypes. The rs6014646 polymorphism was significantly associated with weight loss using co-dominant (p = 0.04) and dominant models (p = 0.03). These p-values were not statistically significant after strict control for multiple testing. Haplotype-based multivariate analysis using permutations showed that rs3827103–rs1543873 (p = 0.06), rs6014646–rs6024730 (p = 0.05) and rs3746619–rs3827103 (p = 0.10) displayed near-statistical significant results in relation to weight loss. No other significant associations or gene*diet interactions were detected for weight loss, fat mass loss, waist change and resting energy expenditure changes. CONCLUSION: The study provided overall sufficient evidence to support that there is no major effect of genetic variants of MC3R and differential weight loss after a 10-week dietary intervention with hypo-energetic diets in obese Europeans.
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spelling pubmed-31148032011-06-21 Allelic Variants of Melanocortin 3 Receptor Gene (MC3R) and Weight Loss in Obesity: A Randomised Trial of Hypo-Energetic High- versus Low-Fat Diets Santos, José L. De la Cruz, Rolando Holst, Claus Grau, Katrine Naranjo, Carolina Maiz, Alberto Astrup, Arne Saris, Wim H. M. MacDonald, Ian Oppert, Jean-Michel Hansen, Torben Pedersen, Oluf Sorensen, Thorkild I. A. Martinez, J. Alfredo PLoS One Research Article INTRODUCTION: The melanocortin system plays an important role in energy homeostasis. Mice genetically deficient in the melanocortin-3 receptor gene have a normal body weight with increased body fat, mild hypophagia compared to wild-type mice. In humans, Thr6Lys and Val81Ile variants of the melanocortin-3 receptor gene (MC3R) have been associated with childhood obesity, higher BMI Z-score and elevated body fat percentage compared to non-carriers. The aim of this study is to assess the association in adults between allelic variants of MC3R with weight loss induced by energy-restricted diets. SUBJECTS AND METHODS: This research is based on the NUGENOB study, a trial conducted to assess weight loss during a 10-week dietary intervention involving two different hypo-energetic (high-fat and low-fat) diets. A total of 760 obese patients were genotyped for 10 single nucleotide polymorphisms covering the single exon of MC3R gene and its flanking regions, including the missense variants Thr6Lys and Val81Ile. Linear mixed models and haplotype-based analysis were carried out to assess the potential association between genetic polymorphisms and differential weight loss, fat mass loss, waist change and resting energy expenditure changes. RESULTS: No differences in drop-out rate were found by MC3R genotypes. The rs6014646 polymorphism was significantly associated with weight loss using co-dominant (p = 0.04) and dominant models (p = 0.03). These p-values were not statistically significant after strict control for multiple testing. Haplotype-based multivariate analysis using permutations showed that rs3827103–rs1543873 (p = 0.06), rs6014646–rs6024730 (p = 0.05) and rs3746619–rs3827103 (p = 0.10) displayed near-statistical significant results in relation to weight loss. No other significant associations or gene*diet interactions were detected for weight loss, fat mass loss, waist change and resting energy expenditure changes. CONCLUSION: The study provided overall sufficient evidence to support that there is no major effect of genetic variants of MC3R and differential weight loss after a 10-week dietary intervention with hypo-energetic diets in obese Europeans. Public Library of Science 2011-06-14 /pmc/articles/PMC3114803/ /pubmed/21695122 http://dx.doi.org/10.1371/journal.pone.0019934 Text en Santos et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Santos, José L.
De la Cruz, Rolando
Holst, Claus
Grau, Katrine
Naranjo, Carolina
Maiz, Alberto
Astrup, Arne
Saris, Wim H. M.
MacDonald, Ian
Oppert, Jean-Michel
Hansen, Torben
Pedersen, Oluf
Sorensen, Thorkild I. A.
Martinez, J. Alfredo
Allelic Variants of Melanocortin 3 Receptor Gene (MC3R) and Weight Loss in Obesity: A Randomised Trial of Hypo-Energetic High- versus Low-Fat Diets
title Allelic Variants of Melanocortin 3 Receptor Gene (MC3R) and Weight Loss in Obesity: A Randomised Trial of Hypo-Energetic High- versus Low-Fat Diets
title_full Allelic Variants of Melanocortin 3 Receptor Gene (MC3R) and Weight Loss in Obesity: A Randomised Trial of Hypo-Energetic High- versus Low-Fat Diets
title_fullStr Allelic Variants of Melanocortin 3 Receptor Gene (MC3R) and Weight Loss in Obesity: A Randomised Trial of Hypo-Energetic High- versus Low-Fat Diets
title_full_unstemmed Allelic Variants of Melanocortin 3 Receptor Gene (MC3R) and Weight Loss in Obesity: A Randomised Trial of Hypo-Energetic High- versus Low-Fat Diets
title_short Allelic Variants of Melanocortin 3 Receptor Gene (MC3R) and Weight Loss in Obesity: A Randomised Trial of Hypo-Energetic High- versus Low-Fat Diets
title_sort allelic variants of melanocortin 3 receptor gene (mc3r) and weight loss in obesity: a randomised trial of hypo-energetic high- versus low-fat diets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114803/
https://www.ncbi.nlm.nih.gov/pubmed/21695122
http://dx.doi.org/10.1371/journal.pone.0019934
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