Abstract

Hereditary mechanisms are partially responsible for individual differences in sensitivity to and the preference for sweet taste. The primary aim of this study was to examine the associations between 10 genetic variants and the intake of total sugar, added sugar, and sugars with sweet taste (i.e., monosaccharides and sucrose) in a middle-aged Swedish population. Two single nucleotide polymorphisms (SNPs) within the Fibroblast grow factor 21 (FGF21) gene, seven top hits from a genome-wide association study (GWAS) on total sugar intake, and one SNP within the fat mass and obesity associated (FTO) gene (the only SNP reaching GWAS significance in a previous study), were explored in relation to various forms of sugar intake in 22,794 individuals from the Malmö Diet and Cancer Study, a population-based cohort for which data were collected between 1991–1996. Significant associations (p = 6.82 × 10−7 − 1.53 × 10−3) were observed between three SNPs (rs838145, rs838133, and rs8103840) in close relation to the FGF21 gene with high Linkage Disequilibrium, and all the studied sugar intakes. For the rs11642841 within the FTO gene, associations were found exclusively among participants with a body mass index ≥ 25 (p < 5 × 10−3). None of the remaining SNPs studied were associated with sugar intake in our cohort. A further GWAS should be conducted to identify novel genetic variants associated with the intake of sugar.

Highlights

  • Over the years, scientific evidence associating sugar intake with non-communicable diseases such as dental caries [1,2], weight gain [3,4], metabolic syndrome, type 2 diabetes [1,2,5], and cardiovascular mortality [1] among others, has continued to increase [6,7]

  • This study explored single-nucleotide polymorphisms (SNPs) that have been previously suggested to be associated with sugar intake and sweet taste preference and sensitivity, in association with an intake of numerous different sugar definitions and different sugar-rich foods and beverages in a Swedish population

  • The strongest associations were found between three variants located within or in close relation to the fibroblast growth factor 21 (FGF21) gene and intakes of added sugar, total sugar, and sugars with a sweet taste, providing additional support for the role of FGF21 in the regulation of sweet taste preference

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Summary

Introduction

Scientific evidence associating sugar intake with non-communicable diseases such as dental caries [1,2], weight gain [3,4], metabolic syndrome, type 2 diabetes [1,2,5], and cardiovascular mortality [1] among others, has continued to increase [6,7]. In GWAS, the fibroblast growth factor 21 (FGF21) gene, the rs838133 SNP and the adjacent rs838145, have been linked to higher intake of carbohydrates and overall caloric intake [13,17,18,19]. This is a well-established region in relation to carbohydrate metabolism and intake, it is understudied regarding specific subgroups of carbohydrate intake, in particular added sugar

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