Publication:
Association of TaqI (rs731236) polymorphism of vitamin D receptor gene with lumbar degenerative disc disease

dc.contributor.coauthorSerifoglu, Luay
dc.contributor.coauthorYilmaz, Seda Gulec
dc.contributor.coauthorKaraaslanli, Abdulmutalip
dc.contributor.coauthorEtli, Mustafa Umut
dc.contributor.coauthorOzdogan, Selcuk
dc.contributor.departmentN/A
dc.contributor.kuauthorDüzkalır, Ali Haluk
dc.contributor.schoolcollegeinstituteN/A
dc.contributor.unitKoç University Hospital
dc.date.accessioned2024-12-29T09:40:11Z
dc.date.issued2024
dc.description.abstract- BACKGROUND: Lumbar degenerative disc disease (LDDD) significantly contributes to low back pain, with a complicated etiology involving genetic and environmental facts. The aim of study was to investigate the association between the Taq I (rs731236) polymorphism of the vitamin D receptor ( VDR ) gene with LDDD. - METHODS: In total, 248 patients with symptomatic LDDD and 146 control subjects were examined. The evaluation of clinical features of patients with LDDD comprised radiodiagnostic magnetic resonance imaging, neurologic examinations, pain scores including the visual analog scale (VAS), and disability investigation with Oswestry Disability Index (ODI). Genotyping of the VDR gene polymorphism was conducted using polymerase chain reaction ebased methods.- RESULTS: Individuals of the LDDD group who were VDR TaqI AA genotype carriers were significantly greater than the other group ( P = 0.014), whereas those with GG genotype were significantly lower ( P = 0.028) in the patient group. In addition, VAS and ODI scores were significantly lower in the GG genotype carrier group, whereas AA genotype carriers had the greatest scores ( P = 0.004). Carrying the G allele decreased the risk of LDDD 1.7 times ( P = 0.014) and carrying the A allele enhanced the risk 1.8 times ( P = 0.028). Moreover, G-allele carriers had significantly lower VAS ( P = 0.002) and ODI scores ( P < 0.0001). - CONCLUSIONS: VDR Taq I (rs731236) GG genotype and G allele have protective potential, whereas the AA genotype and A allele are risk factors for LDDD. The findings reveal a statistically significant association of the Taq I (rs731236) polymorphism of VDR gene polymorphism with LDDD. This result highlights the potential role of genetic factors in developing LDDD and suggests avenues for future research in genetic screening and personalized treatment strategies.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.volume188
dc.identifier.doi10.1016/j.wneu.2024.05.129
dc.identifier.eissn1878-8769
dc.identifier.issn1878-8750
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85196421650
dc.identifier.urihttps://doi.org/10.1016/j.wneu.2024.05.129
dc.identifier.urihttps://hdl.handle.net/20.500.14288/23242
dc.identifier.wos1272597100001
dc.keywordsGenetic risk factors
dc.keywordsLumbar degenerative disc disease
dc.keywordsPolymorphism
dc.keywordsTaqI (rs731236)
dc.keywordsVitamin D receptor gene
dc.languageen
dc.publisherElsevier Science Inc
dc.sourceWorld Neurosurgery
dc.subjectClinical neurology
dc.subjectSurgery
dc.titleAssociation of TaqI (rs731236) polymorphism of vitamin D receptor gene with lumbar degenerative disc disease
dc.typeJournal article
dspace.entity.typePublication
local.contributor.kuauthorDüzkalır, Ali Haluk

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