Association between fok1 polymorphism of vitamin D receptor gene with uterine leiomyoma in Turkish populations

Journal Title: UNKNOWN - Year 2018, Vol 19, Issue 3

Abstract

Objective: The aim of this research was to determine the association between the fok1 polymorphism and uterine leiomyomas. Material and Methods: For genotyping the fok1 polymorphism of the vitamin D receptor, real-time polymerase chain reaction was performed on blood samples of uterine leiomyoma (n=27) and control (n=33) groups. For statistical analyses, SPSS v.23 software (SPSS Inc., Chicago, IL, USA) was used. Results: A statistically significant difference was observed for the frequency of the CC genotype between the uterine leiomyoma and control groups, and the frequencies of the T allele in the uterine leiomyoma groups were significantly higher than in the control group. Conclusion: The presence of the fok1 CC genotype may be a risk-reducing factor and the T allele may be a potential risk factor for developing uterine leiomyoma.

Authors and Affiliations

Seda Güleç Yılmaz, Tuğçe Gül, Rukset Attar, Gazi Yıldırım, Turgay İşbir

Keywords

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  • EP ID EP364927
  • DOI 10.4274/jtgga.2018.0002
  • Views 68
  • Downloads 0

How To Cite

Seda Güleç Yılmaz, Tuğçe Gül, Rukset Attar, Gazi Yıldırım, Turgay İşbir (2018). Association between fok1 polymorphism of vitamin D receptor gene with uterine leiomyoma in Turkish populations. UNKNOWN, 19(3), 128-131. https://www.europub.co.uk/articles/-A-364927