Single nucleotide polymorphisms in sweet, fat, umami, salt, bitter and sour taste receptor genes are associated with gustatory function and taste preferences in young adults

Nutr Res. 2021 Jan:85:40-46. doi: 10.1016/j.nutres.2020.12.007. Epub 2020 Dec 5.

Abstract

Taste is a fundamental mechanism whereby compounds are detected orally, yet it is highly variable among individuals. The variability in taste that is attributable to genetics is not well-characterized despite its potential role in food selection, and therefore, eating habits that contribute to risk of overweight and obesity. In order to implicate measures of taste function and preference as potentially deterministic factors in adverse eating behaviors that lead to obesity, it must be shown that a relationship exists between genetic variation in taste receptor genes and psychophysical measures of taste in the absence high body mass index. The primary objective of this pilot study was to investigate the relationship between single nucleotide polymorphisms (SNPs) in taste receptor genes and 3 different psychophysical measures of taste in healthy young adults. Sweet, salt, umami, fat, sour, and bitter taste receptor gene SNPs were genotyped in 49 participants (ages 24.6 ± 0.6 years) who completed testing to determine oral detection threshold (DT), suprathreshold sensitivity (ST) and taste preference (PR). A simultaneous association test was conducted between each SNP and the 3 taste outcomes (DT, ST, and PR). Twelve SNPs were associated with at least one of the 3 taste outcomes. Associations were observed between SNPs in taste receptor genes and psychophysical measures of sweet, fat, umami, and salt taste. These results suggest that differences in interindividual psychophysical measures of tastes, namely DT, ST, and PR, may be partially attributed to genetic variation in taste receptor genes. Future studies are warranted to investigate if these findings have consequences for habitual dietary intake of foods that elicit these tastes.

Keywords: Human genetics; Nutrigenomics; Nutrition; Sensory; Taste.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Epithelial Sodium Channels / genetics
  • Female
  • Humans
  • Male
  • Pilot Projects
  • Polymorphism, Single Nucleotide*
  • Receptors, Cell Surface / genetics*
  • Receptors, G-Protein-Coupled / genetics*
  • Receptors, Metabotropic Glutamate / genetics
  • TRPV Cation Channels / genetics
  • Taste*
  • Young Adult

Substances

  • Epithelial Sodium Channels
  • Receptors, Cell Surface
  • Receptors, G-Protein-Coupled
  • Receptors, Metabotropic Glutamate
  • TRPV Cation Channels
  • TRPV1 protein, human
  • taste receptors, type 1
  • taste receptors, type 2
  • metabotropic glutamate receptor 4