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The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population

Authors :
Maha Saber-Ayad
Rifat Hamoudi
Rahaf Wardeh
Ahmed Ashraf
Sarah Hammoudeh
Shaista Manzoor
Alsamman M. Alsamman
Peter T. Habib
Hadia Radwan
Hussein Jabbar
Source :
Journal of Advanced Research, Vol 24, Iss, Pp 485-494 (2020), Journal of Advanced Research
Publication Year :
2020
Publisher :
Elsevier, 2020.

Abstract

Graphical abstract<br />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.

Details

Language :
English
ISSN :
20901232
Volume :
24
Database :
OpenAIRE
Journal :
Journal of Advanced Research
Accession number :
edsair.doi.dedup.....0ac0b3357c963b95bfb9eabccca205db