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Gene–diet-related factors of hyperglycaemia in postmenopausal women

As ageing and increased body fat are the signs of insulin resistance, we have studied whether the presence of Pro12Ala and C1431T of peroxisome proliferator-activated receptor gamma 2 gene and Trp64Arg of beta 3-adrenergic receptor gene may predispose to the hyperglycaemia development in postmenopau...

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Autores principales: Grygiel-Górniak, Bogna, Kaczmarek, Elżbieta, Mosor, Maria, Przysławski, Juliusz, Nowak, Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895664/
https://www.ncbi.nlm.nih.gov/pubmed/29464546
http://dx.doi.org/10.1007/s13353-018-0434-9
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author Grygiel-Górniak, Bogna
Kaczmarek, Elżbieta
Mosor, Maria
Przysławski, Juliusz
Nowak, Jerzy
author_facet Grygiel-Górniak, Bogna
Kaczmarek, Elżbieta
Mosor, Maria
Przysławski, Juliusz
Nowak, Jerzy
author_sort Grygiel-Górniak, Bogna
collection PubMed
description As ageing and increased body fat are the signs of insulin resistance, we have studied whether the presence of Pro12Ala and C1431T of peroxisome proliferator-activated receptor gamma 2 gene and Trp64Arg of beta 3-adrenergic receptor gene may predispose to the hyperglycaemia development in postmenopausal women, who have never undergone hypoglycaemic treatment. The distributions of selected allele and genotype frequencies were determined by the PCR–RFLP method in normo- and hyperglycaemic, who have never been diagnosed and treated for diabetes mellitus were measured. The amount of body fat and lean body mass (LBM) were assessed by the bioimpedance method and nutritional habits by 7-day dietary recall. There were no differences between the distribution of genotypes and the allele frequencies of the Pro12Ala, C1431T and Trp64Arg polymorphisms in normo- and hyperglycaemic women. Hyperglycaemic women were characterized by visceral obesity, hypertension, higher serum insulin and triglycerides, higher intake of fat and lower consumption of complex carbohydrates and B vitamins. Normoglycaemic women with Pro12Pro polymorphism acquired higher energy from dietary fat (p < 0.0276) and lower energy from carbohydrates (p < 0.0480) than normoglycaemic Ala12 carriers. Subjects with Pro12Pro polymorphism and LBM > 58% of total body mass or with Trp64Trp and normal triglycerides have higher chance of normoglycaemia. Genotyping for Pro12Ala and Trp64Arg polymorphism in postmenopausal women may have the clinical benefit of predicting hyperglycaemia, thereby contributing to the prevention of diabetes mellitus development in the future. However, not only the genetic background but also the dietary habits (intake of fat, carbohydrates and B vitamins) determine the risk of hyperglycaemia.
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spelling pubmed-58956642018-04-16 Gene–diet-related factors of hyperglycaemia in postmenopausal women Grygiel-Górniak, Bogna Kaczmarek, Elżbieta Mosor, Maria Przysławski, Juliusz Nowak, Jerzy J Appl Genet Human Genetics • Original Paper As ageing and increased body fat are the signs of insulin resistance, we have studied whether the presence of Pro12Ala and C1431T of peroxisome proliferator-activated receptor gamma 2 gene and Trp64Arg of beta 3-adrenergic receptor gene may predispose to the hyperglycaemia development in postmenopausal women, who have never undergone hypoglycaemic treatment. The distributions of selected allele and genotype frequencies were determined by the PCR–RFLP method in normo- and hyperglycaemic, who have never been diagnosed and treated for diabetes mellitus were measured. The amount of body fat and lean body mass (LBM) were assessed by the bioimpedance method and nutritional habits by 7-day dietary recall. There were no differences between the distribution of genotypes and the allele frequencies of the Pro12Ala, C1431T and Trp64Arg polymorphisms in normo- and hyperglycaemic women. Hyperglycaemic women were characterized by visceral obesity, hypertension, higher serum insulin and triglycerides, higher intake of fat and lower consumption of complex carbohydrates and B vitamins. Normoglycaemic women with Pro12Pro polymorphism acquired higher energy from dietary fat (p < 0.0276) and lower energy from carbohydrates (p < 0.0480) than normoglycaemic Ala12 carriers. Subjects with Pro12Pro polymorphism and LBM > 58% of total body mass or with Trp64Trp and normal triglycerides have higher chance of normoglycaemia. Genotyping for Pro12Ala and Trp64Arg polymorphism in postmenopausal women may have the clinical benefit of predicting hyperglycaemia, thereby contributing to the prevention of diabetes mellitus development in the future. However, not only the genetic background but also the dietary habits (intake of fat, carbohydrates and B vitamins) determine the risk of hyperglycaemia. Springer Berlin Heidelberg 2018-02-20 2018 /pmc/articles/PMC5895664/ /pubmed/29464546 http://dx.doi.org/10.1007/s13353-018-0434-9 Text en © The Author(s) 2018 Open Access This 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 Human Genetics • Original Paper
Grygiel-Górniak, Bogna
Kaczmarek, Elżbieta
Mosor, Maria
Przysławski, Juliusz
Nowak, Jerzy
Gene–diet-related factors of hyperglycaemia in postmenopausal women
title Gene–diet-related factors of hyperglycaemia in postmenopausal women
title_full Gene–diet-related factors of hyperglycaemia in postmenopausal women
title_fullStr Gene–diet-related factors of hyperglycaemia in postmenopausal women
title_full_unstemmed Gene–diet-related factors of hyperglycaemia in postmenopausal women
title_short Gene–diet-related factors of hyperglycaemia in postmenopausal women
title_sort gene–diet-related factors of hyperglycaemia in postmenopausal women
topic Human Genetics • Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895664/
https://www.ncbi.nlm.nih.gov/pubmed/29464546
http://dx.doi.org/10.1007/s13353-018-0434-9
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