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Association of vitamin D receptor gene variants with polycystic ovary syndrome: A case control study

BACKGROUND: Vitamin D and insulin play an important role in susceptibility to polycystic ovary syndrome (PCOS), and therefore vitamin D receptor (VDR), parathyroid hormone (PTH), and insulin receptor (INSR) gene variants might be involved in the pathogenesis of PCOS. OBJECTIVE: The present study was...

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Autores principales: Mahmoudi, Touraj, Majidzadeh-A, Keivan, Farahani, Hamid, Mirakhorli, Mojgan, Dabiri, Reza, Nobakht, Hossein, Asadi, Asadollah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Clinical Center for Infertility 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827506/
https://www.ncbi.nlm.nih.gov/pubmed/27141540
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author Mahmoudi, Touraj
Majidzadeh-A, Keivan
Farahani, Hamid
Mirakhorli, Mojgan
Dabiri, Reza
Nobakht, Hossein
Asadi, Asadollah
author_facet Mahmoudi, Touraj
Majidzadeh-A, Keivan
Farahani, Hamid
Mirakhorli, Mojgan
Dabiri, Reza
Nobakht, Hossein
Asadi, Asadollah
author_sort Mahmoudi, Touraj
collection PubMed
description BACKGROUND: Vitamin D and insulin play an important role in susceptibility to polycystic ovary syndrome (PCOS), and therefore vitamin D receptor (VDR), parathyroid hormone (PTH), and insulin receptor (INSR) gene variants might be involved in the pathogenesis of PCOS. OBJECTIVE: The present study was designed to investigate the possible associations between polymorphisms in VDR, PTH, and INSR genes and the risk of PCOS. MATERIALS AND METHODS: VDR, PTH, and INSR gene variants were genotyped in 35 women with PCOS and 35 controls using Polymerase chain reaction – Restriction fragment length polymorphism method. Furthermore, serum levels of glucose and insulin were measured in all participants. RESULTS: No significant differences were observed for the VDR FokI, VDR Tru9I, VDR TaqI, PTH DraII, INSR NsiI, and INSR PmlI gene polymorphisms between the women with PCOS and controls. However, after adjustment for confounding factors, the VDR BsmI “Bb” genotype and the VDR ApaI "Aa" genotype were significantly under transmitted to the patients (p= 0.016; OR= 0.250; 95% CI= 0.081-0.769, and p= 0.017; OR= 0.260; 95% CI= 0.086-0.788, respectively). Furthermore, in the women with PCOS, insulin levels were lower in the participants with the INSR NsiI "NN" genotype compared with those with the "Nn + nn" genotypes (P= 0.045). CONCLUSION: The results showed an association between the VDR gene BsmI and ApaI polymorphisms and PCOS risk. These data also indicated that the INSR "NN" genotype was a marker of decreased insulin in women with PCOS. Our findings, however, do not lend support to the hypothesis that PTH gene DraII variant plays a role in susceptibility to PCOS.
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spelling pubmed-48275062016-05-02 Association of vitamin D receptor gene variants with polycystic ovary syndrome: A case control study Mahmoudi, Touraj Majidzadeh-A, Keivan Farahani, Hamid Mirakhorli, Mojgan Dabiri, Reza Nobakht, Hossein Asadi, Asadollah Int J Reprod Biomed Short Communication BACKGROUND: Vitamin D and insulin play an important role in susceptibility to polycystic ovary syndrome (PCOS), and therefore vitamin D receptor (VDR), parathyroid hormone (PTH), and insulin receptor (INSR) gene variants might be involved in the pathogenesis of PCOS. OBJECTIVE: The present study was designed to investigate the possible associations between polymorphisms in VDR, PTH, and INSR genes and the risk of PCOS. MATERIALS AND METHODS: VDR, PTH, and INSR gene variants were genotyped in 35 women with PCOS and 35 controls using Polymerase chain reaction – Restriction fragment length polymorphism method. Furthermore, serum levels of glucose and insulin were measured in all participants. RESULTS: No significant differences were observed for the VDR FokI, VDR Tru9I, VDR TaqI, PTH DraII, INSR NsiI, and INSR PmlI gene polymorphisms between the women with PCOS and controls. However, after adjustment for confounding factors, the VDR BsmI “Bb” genotype and the VDR ApaI "Aa" genotype were significantly under transmitted to the patients (p= 0.016; OR= 0.250; 95% CI= 0.081-0.769, and p= 0.017; OR= 0.260; 95% CI= 0.086-0.788, respectively). Furthermore, in the women with PCOS, insulin levels were lower in the participants with the INSR NsiI "NN" genotype compared with those with the "Nn + nn" genotypes (P= 0.045). CONCLUSION: The results showed an association between the VDR gene BsmI and ApaI polymorphisms and PCOS risk. These data also indicated that the INSR "NN" genotype was a marker of decreased insulin in women with PCOS. Our findings, however, do not lend support to the hypothesis that PTH gene DraII variant plays a role in susceptibility to PCOS. Research and Clinical Center for Infertility 2015-12 /pmc/articles/PMC4827506/ /pubmed/27141540 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Mahmoudi, Touraj
Majidzadeh-A, Keivan
Farahani, Hamid
Mirakhorli, Mojgan
Dabiri, Reza
Nobakht, Hossein
Asadi, Asadollah
Association of vitamin D receptor gene variants with polycystic ovary syndrome: A case control study
title Association of vitamin D receptor gene variants with polycystic ovary syndrome: A case control study
title_full Association of vitamin D receptor gene variants with polycystic ovary syndrome: A case control study
title_fullStr Association of vitamin D receptor gene variants with polycystic ovary syndrome: A case control study
title_full_unstemmed Association of vitamin D receptor gene variants with polycystic ovary syndrome: A case control study
title_short Association of vitamin D receptor gene variants with polycystic ovary syndrome: A case control study
title_sort association of vitamin d receptor gene variants with polycystic ovary syndrome: a case control study
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827506/
https://www.ncbi.nlm.nih.gov/pubmed/27141540
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