Evidence map›Paper›PMID 42919170›Full record

ArticleGenes & nutrition2026

Genetic variations underlying bitter and sweet taste perception are associated with food and beverage intake habits and taste-modifying behaviors among Dutch adults with a prior myocardial infarction.

Julie E Gervis, Monica Mars, Kamalita Pertiwi, Luc Heerkens, Alice H Lichtenstein, Johanna M Geleijnse

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Article in Genes & nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Julie E GervisJean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA. jgervis@mgh.harvard.edu.ORCID https://orcid.org/0000-0003-0125-9930
Monica MarsDivision of Human Nutrition and Health, Wageningen University and Research, Wageningen, The Netherlands.
Kamalita PertiwiDivision of Human Nutrition and Health, Wageningen University and Research, Wageningen, The Netherlands.
Luc HeerkensDivision of Human Nutrition and Health, Wageningen University and Research, Wageningen, The Netherlands.
Alice H LichtensteinJean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA.
Johanna M GeleijnseDivision of Human Nutrition and Health, Wageningen University and Research, Wageningen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTaste perception influences eating behaviors and varies partly based on genetics. Genome-wide association studies (GWAS) have identified many variants related to bitter, sweet, salt, sour, and umami perception (taste-related variants), but whether these variants inform eating behaviors among patients with cardiovascular disease (CVD) is unknown. This study investigated the associations of taste-related variants with eating behaviors in adults with a prior myocardial infarction (MI) and explored the potential for sex-specific effects.

methodsAnalyzed, were 4,204 Dutch adults with a prior MI from the Alpha Omega Cohort (60-80 years; 21% female; BMI: 27.7 ± 3.8 kg/m MAIN

findings32/39 taste-related variants were nominally (p < 0.05) associated with at least one food or beverage group or taste-modifying behavior, of which 6 passed Bonferroni adjustment (p < 0.05/19 or 0.05/7, respectively). The strongest associations were for rs1726866--a functional variant in the TAS2R38 bitter taste receptor gene--for which each additional G allele related to higher bitter perception was associated with less frequent coffee (β = -1.1 servings/week; 95% CI: -1.75, -0.42) and more frequent tea intake (β = 1.0 servings/week: 95% CI: 0.42, 1.64). Other significant associations were identified for bitter-related variants with less frequent legume intake and addition of full-fat milk to coffee and sweet-related variants with more frequent red/orange vegetable and full-fat dairy intake. Exploratory interaction analyses also suggested potential sex-specific effects; for example, rs1726866 (G) was associated with adding less sugar to coffee among females, but more among males.

conclusionsBitter- and sweet-related variants were associated with food and beverage intake habits and taste-modifying behaviors in adults with a prior MI, with some evidence for sex-specificity. These findings support the relevance of taste-related variants to eating behaviors among CVD patients and suggest the benefit of leveraging these genetic factors when tailoring dietary recommendations for reducing secondary cardiovascular risk.

Indexed as

Dietary intakeGeneticsPrecision nutritionTaste perception

Identifiers

PMID42919170

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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.