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The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population
Food predilection is linked to variants in the hepatokine “Fibroblast Growth Factor-21” gene (FGF21); with rs838133 linked to the sweet tooth in Caucasians. The effect of FGF21 variants on food intake is still unclear in other populations. A cohort of 196 healthy Emirati subjects was investigated [a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296188/ https://www.ncbi.nlm.nih.gov/pubmed/32566284 http://dx.doi.org/10.1016/j.jare.2020.05.020 |
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author | Saber-Ayad, Maha Hammoudeh, Sarah Radwan, Hadia Manzoor, Shaista Jabbar, Hussein Wardeh, Rahaf Ashraf, Ahmed Habib, Peter Alsamman, Alsamman M. Hamoudi, Rifat |
author_facet | Saber-Ayad, Maha Hammoudeh, Sarah Radwan, Hadia Manzoor, Shaista Jabbar, Hussein Wardeh, Rahaf Ashraf, Ahmed Habib, Peter Alsamman, Alsamman M. Hamoudi, Rifat |
author_sort | Saber-Ayad, Maha |
collection | PubMed |
description | Food predilection is linked to variants in the hepatokine “Fibroblast Growth Factor-21” gene (FGF21); with rs838133 linked to the sweet tooth in Caucasians. The effect of FGF21 variants on food intake is still unclear in other populations. A cohort of 196 healthy Emirati subjects was investigated [age: 30.34 ± 9.75yrs (44.4% males)]. The FGF21 rs838133 and rs838145 were genotyped. The daily intake was calculated based on a 61-item food frequency questionnaire. Multivariate analysis was performed using in house R script that implements two-way unsupervised hierarchical clustering to detect the association of the studied single-nucleotide polymorphisms (SNPs) and related SNPs in linkage disequilibrium, using data from the 1000 genome project. Both SNPs were in Hardy-Weinberg Equilaribium (HWE). BMI positively correlated with age (p = 0.002), but not with caloric intake. Salt intake was significantly higher in subjects homozygous (A: rs838133) and (G:rs838145),(p = 0.03 and 0.01, respectively). An interaction was observed between both SNPs; significantly associated with high salt intake. Using publicly available data, both SNPs fall within a region transmitted in Iberians which has a profile closely similar to Caucasians, but far from Chinese population. In conclusion, the minor alleles of FGF21 rs838145 and rs838133 are associated with high salt intake in Emiratis and may suggest neuro-metabolic link to dietary preference across different populations. |
format | Online Article Text |
id | pubmed-7296188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-72961882020-06-18 The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population Saber-Ayad, Maha Hammoudeh, Sarah Radwan, Hadia Manzoor, Shaista Jabbar, Hussein Wardeh, Rahaf Ashraf, Ahmed Habib, Peter Alsamman, Alsamman M. Hamoudi, Rifat J Adv Res Article Food predilection is linked to variants in the hepatokine “Fibroblast Growth Factor-21” gene (FGF21); with rs838133 linked to the sweet tooth in Caucasians. The effect of FGF21 variants on food intake is still unclear in other populations. A cohort of 196 healthy Emirati subjects was investigated [age: 30.34 ± 9.75yrs (44.4% males)]. The FGF21 rs838133 and rs838145 were genotyped. The daily intake was calculated based on a 61-item food frequency questionnaire. Multivariate analysis was performed using in house R script that implements two-way unsupervised hierarchical clustering to detect the association of the studied single-nucleotide polymorphisms (SNPs) and related SNPs in linkage disequilibrium, using data from the 1000 genome project. Both SNPs were in Hardy-Weinberg Equilaribium (HWE). BMI positively correlated with age (p = 0.002), but not with caloric intake. Salt intake was significantly higher in subjects homozygous (A: rs838133) and (G:rs838145),(p = 0.03 and 0.01, respectively). An interaction was observed between both SNPs; significantly associated with high salt intake. Using publicly available data, both SNPs fall within a region transmitted in Iberians which has a profile closely similar to Caucasians, but far from Chinese population. In conclusion, the minor alleles of FGF21 rs838145 and rs838133 are associated with high salt intake in Emiratis and may suggest neuro-metabolic link to dietary preference across different populations. Elsevier 2020-05-21 /pmc/articles/PMC7296188/ /pubmed/32566284 http://dx.doi.org/10.1016/j.jare.2020.05.020 Text en © 2020 THE AUTHORS. Published by Elsevier BV on behalf of Cairo University. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Saber-Ayad, Maha Hammoudeh, Sarah Radwan, Hadia Manzoor, Shaista Jabbar, Hussein Wardeh, Rahaf Ashraf, Ahmed Habib, Peter Alsamman, Alsamman M. Hamoudi, Rifat The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population |
title | The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population |
title_full | The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population |
title_fullStr | The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population |
title_full_unstemmed | The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population |
title_short | The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population |
title_sort | fgf-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the emirati population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296188/ https://www.ncbi.nlm.nih.gov/pubmed/32566284 http://dx.doi.org/10.1016/j.jare.2020.05.020 |
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