» Articles » PMID: 33572225

Genetic Variation in the Bitter Receptors Responsible for Epicatechin Detection Are Associated with BMI in an Elderly Cohort

Overview
Journal Nutrients
Date 2021 Feb 12
PMID 33572225
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Globally, more than one-third of adults are overweight. Overweight and obesity are complex and multifaceted conditions, associated with an increased risk of chronic illness and early mortality. While there are known risk factors, these alone do not fully explain the varying outcomes between individuals. Recently, taste receptors have been proposed to have a role in the risk for obesity. These receptors are expressed throughout the gastrointestinal tract. In this system, they may be involved in modulating dietary intake and metabolic processes. The taste 2 family of receptors (T2Rs) detects bitter compounds. Receptors T2R4 and T2R5 detect (-)-epicatechin (epicatechin), an antioxidant polyphenol, which may have protective effects against obesity. However, the potential role for taste receptors in this association has not been explored. This study assessed whether polymorphisms in (rs2233998 and rs2234001) and (rs2227264) were associated with body mass index (BMI). Genotyping (Taqman qPCR assays) was performed on DNA extracted from blood samples ( = 563) from an elderly cohort. Homozygosity for the minor allele of all polymorphisms was significantly associated with a lower BMI in males. The -rs2233998 CC genotype, the -rs2234001 CC genotype and the -rs2227264 TT genotype were associated with lower BMI (2.1, 2.1 and 2.2 units; = 0.002, 0.003 and 0.001, respectively). Epicatechin intake was not associated with BMI and genotype was not associated with epicatechin intake. This suggests that the association between genotype and elevated BMI risk occurs through altered extra-oral responses and not directly via altered epicatechin intake.

Citing Articles

The identification of a novel shared therapeutic target and drug across all insulin-sensitive tissues under insulin resistance.

Xu J, Zhu L, Xu J, Lin K, Wang J, Bi Y Front Nutr. 2024; 11:1381779.

PMID: 38595789 PMC: 11002099. DOI: 10.3389/fnut.2024.1381779.


Interactions between Beer Compounds and Human Salivary Proteins: Insights toward Astringency and Bitterness Perception.

Goncalves L, Jesus M, Brandao E, Magalhaes P, Mateus N, de Freitas V Molecules. 2023; 28(6).

PMID: 36985492 PMC: 10053927. DOI: 10.3390/molecules28062522.


Effect of Phenolic Compounds on Human Health.

Gonzalez-Burgos E, Gomez-Serranillos M Nutrients. 2021; 13(11).

PMID: 34836177 PMC: 8618337. DOI: 10.3390/nu13113922.

References
1.
Tirosh A, Shai I, Afek A, Dubnov-Raz G, Ayalon N, Gordon B . Adolescent BMI trajectory and risk of diabetes versus coronary disease. N Engl J Med. 2011; 364(14):1315-25. PMC: 4939259. DOI: 10.1056/NEJMoa1006992. View

2.
Boyce J, Shone G . Effects of ageing on smell and taste. Postgrad Med J. 2006; 82(966):239-41. PMC: 2579627. DOI: 10.1136/pgmj.2005.039453. View

3.
Mikolajczyk-Stecyna J, Malinowska A, Chmurzynska A . TAS2R38 and CA6 genetic polymorphisms, frequency of bitter food intake, and blood biomarkers among elderly woman. Appetite. 2017; 116:57-64. DOI: 10.1016/j.appet.2017.04.029. View

4.
Cirera S, Clop A, Jacobsen M, Guerin M, Lesnik P, Jorgensen C . A targeted genotyping approach enhances identification of variants in taste receptor and appetite/reward genes of potential functional importance for obesity-related porcine traits. Anim Genet. 2018; 49(2):110-118. DOI: 10.1111/age.12641. View

5.
Wicks D, Wright J, Rayment P, Spiller R . Impact of bitter taste on gastric motility. Eur J Gastroenterol Hepatol. 2005; 17(9):961-5. DOI: 10.1097/00042737-200509000-00012. View