Title of article
Vitamin D Receptor TaqI Gene Variant in Exon 9 and Polycystic Ovary Syndrome Risk
Author/Authors
Bagheri، Morteza نويسنده Genetics Department, Urmia University of Medical Sciences, Urmia, Iran , , Abdi-Rad، Isa نويسنده , , Hosseini Jazani، Nima نويسنده Food and Beverages Safety Research Center, Urmia University of Medical Sciences, Urmia, Iran , , Nanbakhsh، Fariba نويسنده Obstetrics and Gynecology Department, Urmia University of Medical Sciences, Urmia, Iran ,
Issue Information
فصلنامه با شماره پیاپی 26 سال 2013
Pages
6
From page
116
To page
121
Abstract
Background: Polycystic ovary syndrome (PCOS) is known as a metabolic disorder.
The results of recent studies implied that vitamin D receptor (VDR) genetic
variants may impact PCOS and insulin resistance in women with PCOS. The aim
of the present study was to determine the VDR TaqI gene variant in exon 9 (T/C)
(rs731236) in normal controls and patients with PCOS for the first time in Iranian
Azeri women.
Materials and Methods: In this case control study between April 2011 and June 2012,
a total of 76 women aged 18-40 years (38 patients with PCOS and 38 healthy women
as normal controls) participated. Genotypes of VDR TaqI in exon 9 (T/C) (rs731236)
were determined using the PCR-RFLP method.
Results: The frequencies of VDR TaqI T anc C alleles were 0.605 and 0.395 in cases
and 0.697 and 0.303 in controls. Also, the genotypic frequencies of VDR TaqI were
16) (42.11), 14(36.84), and 8(21.05) in cases, and 17(44.74), 19(50), and 2(5.26)
in controls for TT, TC and CC genotypes respectively. There was no difference in
genotype and allele frequencies between PCOS and controls (p value > 0.05) with
the exception of the CC genotype (p value=0.04).
Conclusion: This report, a first of its own kind in Iranian Azeri patients, suggests that the
CC genotype of VDR TaqI in exon 9 (rs731236) is associated with PCOS.
Journal title
International Journal of Fertility and Sterility
Serial Year
2013
Journal title
International Journal of Fertility and Sterility
Record number
883859
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