Cargando…

The MC4R genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans

PURPOSE: The interactions between lifestyle and genetic factors play an important role in obesity development. Mutations in melanocortin-4-receptor (MC4R) gene are one of the most common cause of monogenic obesity, however, the functional effects of polymorphic variants near MC4R gene in general pop...

Descripción completa

Detalles Bibliográficos
Autores principales: Adamska-Patruno, Edyta, Goscik, Joanna, Czajkowski, Przemyslaw, Maliszewska, Katarzyna, Ciborowski, Michał, Golonko, Anna, Wawrusiewicz-Kurylonek, Natalia, Citko, Anna, Waszczeniuk, Magdalena, Kretowski, Adam, Gorska, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768895/
https://www.ncbi.nlm.nih.gov/pubmed/30945034
http://dx.doi.org/10.1007/s00394-019-01955-0
_version_ 1783455142968819712
author Adamska-Patruno, Edyta
Goscik, Joanna
Czajkowski, Przemyslaw
Maliszewska, Katarzyna
Ciborowski, Michał
Golonko, Anna
Wawrusiewicz-Kurylonek, Natalia
Citko, Anna
Waszczeniuk, Magdalena
Kretowski, Adam
Gorska, Maria
author_facet Adamska-Patruno, Edyta
Goscik, Joanna
Czajkowski, Przemyslaw
Maliszewska, Katarzyna
Ciborowski, Michał
Golonko, Anna
Wawrusiewicz-Kurylonek, Natalia
Citko, Anna
Waszczeniuk, Magdalena
Kretowski, Adam
Gorska, Maria
author_sort Adamska-Patruno, Edyta
collection PubMed
description PURPOSE: The interactions between lifestyle and genetic factors play an important role in obesity development. Mutations in melanocortin-4-receptor (MC4R) gene are one of the most common cause of monogenic obesity, however, the functional effects of polymorphic variants near MC4R gene in general populations remain uncertain. The aim of our study was to analyze whether the common single nucleotide polymorphisms (SNPs) of MC4R gene influence the food preferences, physical activity, body fat content and distribution, as well as fasting and postprandial energy expenditure and substrates utilization. METHODS: We genotyped previously identified MC4R SNPs: rs17782313, rs633265, rs1350341, rs12970134 in 927 subjects, who underwent anthropometric, total body fat content, visceral (VAT) and subcutaneous adipose tissue (SAT) measurements, and daily physical activity and dietary intake analysis. In randomly selected 47 subjects the energy expenditure, carbohydrate and lipid utilizations were evaluated in fasting state and after high-carbohydrate and control meals intake. RESULTS: We found the significant associations between studied SNPs of MC4R gene and VAT and VAT/SAT ratio. Moreover, the GG genotype carriers of rs1350341, who had the lowest VAT accumulation (p = 0.012), presented higher relative increase in postprandial carbohydrate utilization (p = 0.013, p = 0.024). CONCLUSIONS: We have observed that common SNPs of the MC4R gene influence the body fat content and distribution, as well as relative increase in postprandial carbohydrate utilization. We believe that our study may help to understand better the impact of MC4R gene on obesity development, and to help to provide personalized prevention/treatment strategies to fight against obesity and its metabolic consequences.
format Online
Article
Text
id pubmed-6768895
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-67688952019-10-16 The MC4R genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans Adamska-Patruno, Edyta Goscik, Joanna Czajkowski, Przemyslaw Maliszewska, Katarzyna Ciborowski, Michał Golonko, Anna Wawrusiewicz-Kurylonek, Natalia Citko, Anna Waszczeniuk, Magdalena Kretowski, Adam Gorska, Maria Eur J Nutr Original Contribution PURPOSE: The interactions between lifestyle and genetic factors play an important role in obesity development. Mutations in melanocortin-4-receptor (MC4R) gene are one of the most common cause of monogenic obesity, however, the functional effects of polymorphic variants near MC4R gene in general populations remain uncertain. The aim of our study was to analyze whether the common single nucleotide polymorphisms (SNPs) of MC4R gene influence the food preferences, physical activity, body fat content and distribution, as well as fasting and postprandial energy expenditure and substrates utilization. METHODS: We genotyped previously identified MC4R SNPs: rs17782313, rs633265, rs1350341, rs12970134 in 927 subjects, who underwent anthropometric, total body fat content, visceral (VAT) and subcutaneous adipose tissue (SAT) measurements, and daily physical activity and dietary intake analysis. In randomly selected 47 subjects the energy expenditure, carbohydrate and lipid utilizations were evaluated in fasting state and after high-carbohydrate and control meals intake. RESULTS: We found the significant associations between studied SNPs of MC4R gene and VAT and VAT/SAT ratio. Moreover, the GG genotype carriers of rs1350341, who had the lowest VAT accumulation (p = 0.012), presented higher relative increase in postprandial carbohydrate utilization (p = 0.013, p = 0.024). CONCLUSIONS: We have observed that common SNPs of the MC4R gene influence the body fat content and distribution, as well as relative increase in postprandial carbohydrate utilization. We believe that our study may help to understand better the impact of MC4R gene on obesity development, and to help to provide personalized prevention/treatment strategies to fight against obesity and its metabolic consequences. Springer Berlin Heidelberg 2019-04-03 2019 /pmc/articles/PMC6768895/ /pubmed/30945034 http://dx.doi.org/10.1007/s00394-019-01955-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Contribution
Adamska-Patruno, Edyta
Goscik, Joanna
Czajkowski, Przemyslaw
Maliszewska, Katarzyna
Ciborowski, Michał
Golonko, Anna
Wawrusiewicz-Kurylonek, Natalia
Citko, Anna
Waszczeniuk, Magdalena
Kretowski, Adam
Gorska, Maria
The MC4R genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans
title The MC4R genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans
title_full The MC4R genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans
title_fullStr The MC4R genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans
title_full_unstemmed The MC4R genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans
title_short The MC4R genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans
title_sort mc4r genetic variants are associated with lower visceral fat accumulation and higher postprandial relative increase in carbohydrate utilization in humans
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768895/
https://www.ncbi.nlm.nih.gov/pubmed/30945034
http://dx.doi.org/10.1007/s00394-019-01955-0
work_keys_str_mv AT adamskapatrunoedyta themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT goscikjoanna themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT czajkowskiprzemyslaw themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT maliszewskakatarzyna themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT ciborowskimichał themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT golonkoanna themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT wawrusiewiczkuryloneknatalia themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT citkoanna themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT waszczeniukmagdalena themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT kretowskiadam themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT gorskamaria themc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT adamskapatrunoedyta mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT goscikjoanna mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT czajkowskiprzemyslaw mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT maliszewskakatarzyna mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT ciborowskimichał mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT golonkoanna mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT wawrusiewiczkuryloneknatalia mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT citkoanna mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT waszczeniukmagdalena mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT kretowskiadam mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans
AT gorskamaria mc4rgeneticvariantsareassociatedwithlowervisceralfataccumulationandhigherpostprandialrelativeincreaseincarbohydrateutilizationinhumans