# Folate Status Shaped by Taste Receptor Genetics and Sociobehavioral Modulation: Evidence from a Hungarian Cohort

**Authors:** Peter Piko, Judit Dioszegi, Nora Kovacs, Roza Adany

PMC · DOI: 10.3390/nu18040562 · Nutrients · 2026-02-08

## TL;DR

This study shows that genetics related to bitter taste receptors influence folate levels in a Hungarian population, with education playing a role in how this genetic effect manifests.

## Contribution

The study identifies a genetic polygenic score for taste receptors as a novel predictor of serum folate levels, independent of dietary intake.

## Key findings

- TAS2R19 rs10772420 was the strongest genetic predictor of serum folate levels.
- The taste-related polygenic score showed a dose–response relationship with folate levels.
- Higher education amplified the genetic associations with folate levels.

## Abstract

Background: Folate is essential for one-carbon metabolism, yet deficiency remains common in non-fortified populations. Bitter-taste-receptor genetics may influence vegetable intake and thus folate status, but the cumulative impact of sensory genetics, diet, and sociodemographic factors is unclear. This study aimed to investigate how taste-related genetic variants, aggregated into a polygenic score (PGS), together with dietary behavior and sociodemographic factors, modulate serum folate levels in a Hungarian adult population, including Roma ethnic minority participants. Methods: In a cross-sectional sample of 626 adults (312 from the Hungarian general population and 314 from the Roma ethnic minority), serum folate was quantified by chemiluminescent immunoassay, and eight taste-related single-nucleotide polymorphisms (SNPs) were genotyped. A four-SNP PGS (TAS2R19 rs10772420, OR10G4 rs1527483, TRPV1 rs8065080, and CD36 rs1761667) was optimized via the stepwise method (ΔR2 criterion, FDR q < 0.05). Multivariable linear regression was used to assess associations with continuous folate, and logistic models were used to evaluate deficiency risk (≤13 µmol/L; area under the curve, AUC). Interaction terms were tested for effect modification by education and vegetable intake, and mediation pathways were examined by structural equation modeling with 1000 bootstrap replications. Results: TAS2R19 rs10772420 was found to be the strongest predictor of serum folate level. This effect remained significant even after adjusting for vegetable intake (β = 1.12 nmol/L; p = 0.003), suggesting a persistent genetic association independent of vegetable intake. The taste-related PGS exhibited a significant dose–response relationship with folate levels (p < 0.001) but had only modest discriminatory power for deficiency (AUC = 0.569). Higher educational attainment amplified the associations between the PGS and folate levels (p for interaction < 0.05), whereas vegetable intake did not mediate genetic effects. The associations were consistent across Hungarian general and Roma population subgroups. Conclusions: Bitter-taste-receptor genetics are associated with serum folate levels in a pattern not substantially mediated by self-reported vegetable intake, and this influence is further modified by education. These findings support the development of genome-informed, culturally tailored nutrition strategies for non-fortified populations.

## Linked entities

- **Genes:** TAS2R19 (taste 2 receptor member 19) [NCBI Gene 259294], OR10G4 (olfactory receptor family 10 subfamily G member 4) [NCBI Gene 390264], TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442], CD36 (CD36 molecule (CD36 blood group)) [NCBI Gene 948]

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, MTHFR (methylenetetrahydrofolate reductase) [NCBI Gene 4524], OR10G4 (olfactory receptor family 10 subfamily G member 4) [NCBI Gene 390264] {aka OR11-278}, FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, FOLR1 (folate receptor alpha) [NCBI Gene 2348] {aka FBP, FOLR, FR-alpha, FRalpha, NCFTD}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, DHFR (dihydrofolate reductase) [NCBI Gene 1719] {aka DHFR1, DYR}, GGTLC4P (gamma-glutamyltransferase light chain 4 pseudogene) [NCBI Gene 729838] {aka GGT}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, TAS2R19 (taste 2 receptor member 19) [NCBI Gene 259294] {aka MSTP058, T2R19, T2R23, T2R48, TAS2R23, TAS2R48}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}
- **Diseases:** systemic (MESH:D015619), noncommunicable diseases (MESH:D000073296), developmental disorders (MESH:D002658), NTDs (MESH:D009436), Bitter taste (MESH:D013651), metabolic syndrome (MESH:D024821), injury to (MESH:D014947), inflammation (MESH:D007249), folate deficiency (MESH:C562799), gastrointestinal pathology (MESH:D005767), insulin resistance (MESH:D007333)
- **Chemicals:** lipid (MESH:D008055), Alcohol (MESH:D000438), Folate (MESH:D005492), glucose (MESH:D005947), creatinine (MESH:D003404), cholesterol (MESH:D002784), PGS (-), Sugar (MESH:D000073893), Salt (MESH:D012492), uric acid (MESH:D014527), EDTA (MESH:D004492), homocysteine (MESH:D006710), triglyceride (MESH:D014280)
- **Species:** Spinacia oleracea (spinach, species) [taxon 3562], Citrus x paradisi (grapefruit, species) [taxon 37656], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs3785368, rs239345, A1C, rs2274333, AUC of 0, rs1527483, 1911 A>G, rs713598, rs10772420, rs1761667, rs307355

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12943046/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943046/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943046/full.md

---
Source: https://tomesphere.com/paper/PMC12943046