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Title

Investigation of the FSHR, CYP11, and INSR Mutations and Polymorphisms in Iranian Infertile Women with Polycystic Ovary Syndrome (PCOS)

مجله گزارش های بیوشیمی و زیست شناسی مولکولی، دوره: 9، شماره: 4
Year: 1399
COI: JR_RBMB-9-4_013
Language: EnglishView: 108
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Authors

Elaheh Seyed Abutorabi - Vali-e-Asr Reproductive Health Research center, Tehran University of Medical Sciences, Tehran, Iran
Batool Hossein Rashidi - Vali-e-Asr Reproductive Health Research center, Tehran University of Medical Sciences, Tehran, Iran
Shiva Irani - Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Fedyeh Haghollahi - Vali-e-Asr Reproductive Health Research center, Tehran University of Medical Sciences, Tehran, Iran
Maryam Bagheri - Vali-e-Asr Reproductive Health Research center, Tehran University of Medical Sciences, Tehran, Iran

Abstract:

Introduction: polycystic ovary syndrome (PCOS) is the most common cause of ovarian dysfunction associated with infertility, Oligomenorrhea or amenorrhea, hirsutism, acne, and obesity. A large body of evidence unraveled, three major groups of genes play critical roles in underlying PCOS molecular mechanism. The aim of this study is to investigate critical exonic variant of FSHR, CYP11, and INSR and determine the functionality of these mutations in Iranian patients with PCOS. Materials and methods: In this case-control study, 130 patients with PCOS who referred to the Vali-e-Asr Hospital with infertility were included. 3 ml peripheral blood was taken from the participants for DNA extraction. PCR was conducted for each gene and the PCR product was genotyped by sequencing. Results: The data showed that there were two polymorphisms in INSR genes which did not change the protein sequences; these alterations can also be considered as a single nucleotide polymorphism (SNP). Moreover, any exonic variant has not been detected in CYP11B1. Whereas, two missense mutation have been detected in FSHR gene including p.Ala307Thr and p. Asn680Ser. It has been shown that the polymorphisms of the FSHR gene affect the hormone response in the ovaries. Our data demonstrated that the FSHR mutations frequencies were higher in the patients with PCOS rather than control people (without any infertility complication) significantly. Conclusion: Altogether, our data showed that the polymorphisms of FSHR were significantly associated with PCOS in Iranian infertile women. Further studies with larger sample sizes are needed to be performed in order to explore the strength of the association.  

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This Paper COI Code is JR_RBMB-9-4_013. Also You can use the following address to link to this article. This link is permanent and is used as an article registration confirmation in the Civilica reference:

https://civilica.com/doc/1177957/

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Seyed Abutorabi, Elaheh and Hossein Rashidi, Batool and Irani, Shiva and Haghollahi, Fedyeh and Bagheri, Maryam,1399,Investigation of the FSHR, CYP11, and INSR Mutations and Polymorphisms in Iranian Infertile Women with Polycystic Ovary Syndrome (PCOS),https://civilica.com/doc/1177957

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Type of center: علوم پزشکی
Paper count: 9,440
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