Evidence map›Paper›PMID 40353482›Full record

ArticleActa otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale2025

The impact of the bitter taste receptor on the predisposition to chronic rhinosinusitis.

Karolina Dżaman, Karolina Piskadło-Zborowska, Katarzyna Czerwaty, Rafał Jowik, Małgorzata Stachowiak, Elżbieta Sarnowska

Abstract read
In one paragraph

Article in Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Direct Maxillary Sinus Tissue Analysis forJournal of clinical medicine · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Karolina DżamanDepartment of Otolaryngology, Centre of Postgraduate Medical Education, Marymoncka, Warsaw, Poland.
Karolina Piskadło-ZborowskaFaculty of Medicine, Collegium Medicum, Cardinal Stefan Wyszynski University, Dewajtis, Warsaw, Poland.
Katarzyna CzerwatyDepartment of Otolaryngology, Centre of Postgraduate Medical Education, Marymoncka, Warsaw, Poland.
Rafał JowikFaculty of Medicine, Collegium Medicum, Cardinal Stefan Wyszynski University, Dewajtis, Warsaw, Poland.
Małgorzata StachowiakDepartment of Experimental Immunotherapy, Maria Sklodowska, Curie Institute, Oncology Center, Roentgena , Warsaw, Poland.
Elżbieta SarnowskaDepartment of Experimental Immunotherapy, Maria Sklodowska, Curie Institute, Oncology Center, Roentgena , Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Genetic polymorphisms in bitter taste receptor 2 member 38 (TAS2R38), expressed in the cilia of sinonasal epithelial cells, have been proposed to be contributors to chronic rhinosinusitis (CRS). Methods: We assessed the impact of the genetically determined TAS2R38 structure on predisposition to CRS and correlated the expression of the TAS2R38 with haplotypes. 86 patients (60 CRS patients, 26 controls) undergoing nasal surgery were enrolled. PCR to identify single nucleotide polymorphisms in genes encoding TAS2R38 were performed. TAS2R38 expression in sinus mucosa tissues was assessed by immunohistochemistry. Results: Among CRS patients, the protective genotype PAV/PAV of the TAS2R38 was observed with the lowest frequency. Immunohistochemistry displayed significant overexpression of TAS2R38 in patients with CRS and in those with a non-functional AVI/AVI genotype. Under inflammatory conditions, TAS2R38 was found to translocate from the cell membrane. Conclusions: Genetically determined TAS2R38 polymorphisms may influence susceptibility to CRS. The AVI haplotype seems to be an independent risk factor for CRS. Additionally, TAS2Rs and related signalling pathways might create a unique group of therapeutic targets in CRS.

Indexed as

Genetic Predisposition to DiseaseReceptors, G-Protein-CoupledRhinitisSinusitisAdultAgedChronic DiseaseFemaleHumansMaleMiddle AgedPolymorphism, Single NucleotideRhinosinusitisTaste Receptors, Type 2Receptors, G-Protein-CoupledTaste Receptors, Type 2bitter taste receptorchronic rhinosinusitisCRSgeneticsTAS2R38

Identifiers

PMID40353482
PMCPMC12068522

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Registered trials

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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.