Evidence map›Paper›PMID 40498099›Full record

ArticleEuropean journal of nutrition2025

Phenome-wide investigation of dietary and health outcomes associated with bitter taste receptor gene TAS2R38.

Caroline Brito Nunes, Amanda Wei-Yin Lim, Quimbe Dy, Jue-Sheng Ong, Liang-Dar Hwang

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Article in European journal of nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Caroline Brito NunesInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD, Australia.
Amanda Wei-Yin LimQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Quimbe DyInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD, Australia.
Jue-Sheng OngQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Liang-Dar HwangInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD, Australia. d.hwang@uq.edu.au.ORCID http://orcid.org/0000-0002-5535-2199

Funding

Australian Research Council DE240100014National Health and Medical Research Council 2018420
6 · The paper itself

Abstract

backgroundBitter taste receptor gene TAS2R38 determines our ability to perceive the bitter substances phenylthiocarbamide (PTC) and propylthiouracil (PROP). Despite being extensively investigated, its potential correlations with dietary and health outcomes remain inconclusive. This study aims to validate previous findings observed in small studies and explore novel associations using publicly available summary results statistics from large-scale genome-wide association studies (GWAS).

methodsWe examine the associations between three TAS2R38 variants (rs713598, rs1726866, and rs10246939) and 139 food liking traits and 29 food intake traits using GWAS data from the UK Biobank (N up to 445,779 individuals of European ancestry). We further search for their associations with health outcomes in published GWASs using three online platforms OpenGWAS, Open Targets, and GWAS Atlas.

resultsThe bitter sensitive alleles were associated with reduced preferences for and/or consumption of horseradish, salty food, grapefruit, and alcohol (but only for whiskey, red wine, and spirits), increased preferences for cucumber and melon, and increased consumption of tea (p < Bonferroni-corrected threshold of 0.00128). We identified novel associations between bitter sensitive alleles and impaired renal function, indicated by increased serum creatinine levels (p = 9.80 × 10

conclusionThis study highlights the potential impact of the TAS2R38 genotype on food preference, consumption, renal function, and bipolar disorder. Further research on genetic links will facilitate the development of targeted interventions and public health strategies to mitigate diet-related health risks.

Indexed as

DietFood PreferencesPhenomicsReceptors, G-Protein-CoupledTasteFemaleGenome-Wide Association StudyHumansMaleMiddle AgedPolymorphism, Single NucleotideTaste Receptors, Type 2United KingdomReceptors, G-Protein-CoupledTaste Receptors, Type 2Food intakeGenome-wide association studiesPhenome-wide association studiesSupertasterTAS2R38UK Biobank

Identifiers

PMID40498099
PMCPMC12158849

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.