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ArticleMolecular biology reports2026

Vitamin D receptor rs2228570 (FokI) variant is associated with chronic tinnitus susceptibility.

Hilal Akalin, Nuriye Gokce, Servet Akyuz, Olcay Boyacioglu, Seda Orenay-Boyacioglu

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Article in Molecular biology reports, 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

5 authors.

Hilal AkalinDeparment of Medical Genetics, School of Medicine, Erciyes University, Kayseri, 38030, Melikgazi, Türkiye.ORCID http://orcid.org/0000-0002-2580-836X
Nuriye GokceDeparment of Medical Genetics, School of Medicine, Erciyes University, Kayseri, 38030, Melikgazi, Türkiye.ORCID http://orcid.org/0000-0001-7814-5224
Servet AkyuzDeparment of Otolaryngology, School of Medicine, Aydin Adnan Menderes University, Aydin, 09010, Efeler, Türkiye.
Olcay BoyaciogluDepartment of Food Engineering, Faculty of Engineering, Aydin Adnan Menderes University, Aydin, 09010, Efeler, Türkiye.ORCID http://orcid.org/0000-0003-0436-3020
Seda Orenay-BoyaciogluDeparment of Medical Genetics, School of Medicine, Aydin Adnan Menderes University, Aydin, 09010, Efeler, Türkiye. sorenay@adu.edu.tr.ORCID http://orcid.org/0000-0003-1651-1940

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTinnitus is a multifactorial condition with complex and not fully elucidated pathophysiology. Emerging evidence suggests that vitamin D deficiency and neuroinflammatory mechanisms may contribute to tinnitus development. Although vitamin D receptor (VDR) gene polymorphisms have been investigated in otologic disorders, their association with chronic tinnitus remains unclear. This study aimed to evaluate the relationship between VDR polymorphisms and chronic tinnitus susceptibility.

methodsThis case-control study included 208 participants (104 chronic tinnitus patients and 104 healthy controls). Four VDR polymorphisms (rs2228570/FokI, rs1544410/BsmI, rs7975232/ApaI, and rs731236/TaqI) were genotyped using real-time PCR. Genotype and allele frequencies were analyzed under dominant, recessive, and additive models. Haplotype distributions were estimated using the Expectation-Maximization algorithm. Bonferroni correction was applied for multiple testing. Cis-eQTL analyses were conducted using GTEx v8 data, and functional annotations were assessed using public databases.

resultsAmong the analyzed variants, only FokI showed a significant association with chronic tinnitus at the allelic level after multiple comparison correction (p = 0.011). The C allele was more frequent in patients, whereas the T allele appeared protective. No significant associations were observed for BsmI, ApaI, and TaqI. Haplotype analyses yielded nominal findings that did not remain significant after correction. Cis-eQTL evaluation revealed no significant relationship between FokI genotype and VDR expression levels in brain tissues or whole blood. Functional annotation suggested a potential effect on receptor isoform structure.

conclusionThe VDR FokI polymorphism may be associated with susceptibility to chronic tinnitus. However, the underlying biological mechanisms remain to be elucidated and require further investigation.

Indexed as

Receptors, CalcitriolTinnitusAdultAllelesCase-Control StudiesChronic DiseaseFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHaplotypesHumansMaleMiddle AgedPolymorphism, Single NucleotideReceptors, CalcitriolVDR protein, humanGene Expression RegulationGenotypePolymorphism, Single Nucleotiders2228570TinnitusVitamin D Receptor

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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 Socratic graph.