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Interaction between Metabolic Genetic Risk Score and Dietary Fatty Acid Intake on Central Obesity in a Ghanaian Population
Obesity is a multifactorial condition arising from the interaction between genetic and lifestyle factors. We aimed to assess the impact of lifestyle and genetic factors on obesity-related traits in 302 healthy Ghanaian adults. Dietary intake and physical activity were assessed using a 3 day repeated...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400498/ https://www.ncbi.nlm.nih.gov/pubmed/32605047 http://dx.doi.org/10.3390/nu12071906 |
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author | Alsulami, Sooad Nyakotey, David A. Dudek, Kamila Bawah, Abdul-Malik Lovegrove, Julie A. Annan, Reginald A. Ellahi, Basma Vimaleswaran, Karani Santhanakrishnan |
author_facet | Alsulami, Sooad Nyakotey, David A. Dudek, Kamila Bawah, Abdul-Malik Lovegrove, Julie A. Annan, Reginald A. Ellahi, Basma Vimaleswaran, Karani Santhanakrishnan |
author_sort | Alsulami, Sooad |
collection | PubMed |
description | Obesity is a multifactorial condition arising from the interaction between genetic and lifestyle factors. We aimed to assess the impact of lifestyle and genetic factors on obesity-related traits in 302 healthy Ghanaian adults. Dietary intake and physical activity were assessed using a 3 day repeated 24 h dietary recall and global physical activity questionnaire, respectively. Twelve single nucleotide polymorphisms (SNPs) were used to construct 4-SNP, 8-SNP and 12-SNP genetic risk scores (GRSs). The 4-SNP GRS showed significant interactions with dietary fat intakes on waist circumference (WC) (Total fat, P(interaction) = 0.01; saturated fatty acids (SFA), P(interaction) = 0.02; polyunsaturated fatty acids (PUFA), P(interaction) = 0.01 and monounsaturated fatty acids (MUFA), P(interaction) = 0.01). Among individuals with higher intakes of total fat (>47 g/d), SFA (>14 g/d), PUFA (>16 g/d) and MUFA (>16 g/d), individuals with ≥3 risk alleles had a significantly higher WC compared to those with <3 risk alleles. This is the first study of its kind in this population, suggesting that a higher consumption of dietary fatty acid may have the potential to increase the genetic susceptibility of becoming centrally obese. These results support the general dietary recommendations to decrease the intakes of total fat and SFA, to reduce the risk of obesity, particularly in individuals with a higher genetic predisposition to central obesity. |
format | Online Article Text |
id | pubmed-7400498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74004982020-08-07 Interaction between Metabolic Genetic Risk Score and Dietary Fatty Acid Intake on Central Obesity in a Ghanaian Population Alsulami, Sooad Nyakotey, David A. Dudek, Kamila Bawah, Abdul-Malik Lovegrove, Julie A. Annan, Reginald A. Ellahi, Basma Vimaleswaran, Karani Santhanakrishnan Nutrients Article Obesity is a multifactorial condition arising from the interaction between genetic and lifestyle factors. We aimed to assess the impact of lifestyle and genetic factors on obesity-related traits in 302 healthy Ghanaian adults. Dietary intake and physical activity were assessed using a 3 day repeated 24 h dietary recall and global physical activity questionnaire, respectively. Twelve single nucleotide polymorphisms (SNPs) were used to construct 4-SNP, 8-SNP and 12-SNP genetic risk scores (GRSs). The 4-SNP GRS showed significant interactions with dietary fat intakes on waist circumference (WC) (Total fat, P(interaction) = 0.01; saturated fatty acids (SFA), P(interaction) = 0.02; polyunsaturated fatty acids (PUFA), P(interaction) = 0.01 and monounsaturated fatty acids (MUFA), P(interaction) = 0.01). Among individuals with higher intakes of total fat (>47 g/d), SFA (>14 g/d), PUFA (>16 g/d) and MUFA (>16 g/d), individuals with ≥3 risk alleles had a significantly higher WC compared to those with <3 risk alleles. This is the first study of its kind in this population, suggesting that a higher consumption of dietary fatty acid may have the potential to increase the genetic susceptibility of becoming centrally obese. These results support the general dietary recommendations to decrease the intakes of total fat and SFA, to reduce the risk of obesity, particularly in individuals with a higher genetic predisposition to central obesity. MDPI 2020-06-27 /pmc/articles/PMC7400498/ /pubmed/32605047 http://dx.doi.org/10.3390/nu12071906 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Alsulami, Sooad Nyakotey, David A. Dudek, Kamila Bawah, Abdul-Malik Lovegrove, Julie A. Annan, Reginald A. Ellahi, Basma Vimaleswaran, Karani Santhanakrishnan Interaction between Metabolic Genetic Risk Score and Dietary Fatty Acid Intake on Central Obesity in a Ghanaian Population |
title | Interaction between Metabolic Genetic Risk Score and Dietary Fatty Acid Intake on Central Obesity in a Ghanaian Population |
title_full | Interaction between Metabolic Genetic Risk Score and Dietary Fatty Acid Intake on Central Obesity in a Ghanaian Population |
title_fullStr | Interaction between Metabolic Genetic Risk Score and Dietary Fatty Acid Intake on Central Obesity in a Ghanaian Population |
title_full_unstemmed | Interaction between Metabolic Genetic Risk Score and Dietary Fatty Acid Intake on Central Obesity in a Ghanaian Population |
title_short | Interaction between Metabolic Genetic Risk Score and Dietary Fatty Acid Intake on Central Obesity in a Ghanaian Population |
title_sort | interaction between metabolic genetic risk score and dietary fatty acid intake on central obesity in a ghanaian population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400498/ https://www.ncbi.nlm.nih.gov/pubmed/32605047 http://dx.doi.org/10.3390/nu12071906 |
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