Mutation analysis of exon1 of bone morphogenetic protein-15 gene in Iranian patients with polycystic ovarian syndrome

Background: With the prevalence of 6-10%, polycystic ovarian syndrome (PCOS) is considered the most common endocrinological disorder affecting women in their reproductive age. It has been suggested that genetic factors participate in the development of PCOS. Follicular development has been considere...

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Main Authors: Anahita Mehdizadeh (Author), Mohammad Hasan Sheikhha (Author), Seyed Mehdi Kalantar (Author), Bibi Shahnaz Aali (Author), Azam Ghanei (Author)
Format: Book
Published: Shahid Sadoughi University of Medical Science, Yazd, Iran, 2016-08-01T00:00:00Z.
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001 doaj_8ee0cda0b9ee4ef9af0f739a77eea0c9
042 |a dc 
100 1 0 |a Anahita Mehdizadeh  |e author 
700 1 0 |a Mohammad Hasan Sheikhha  |e author 
700 1 0 |a Seyed Mehdi Kalantar  |e author 
700 1 0 |a Bibi Shahnaz Aali  |e author 
700 1 0 |a Azam Ghanei  |e author 
245 0 0 |a Mutation analysis of exon1 of bone morphogenetic protein-15 gene in Iranian patients with polycystic ovarian syndrome 
260 |b Shahid Sadoughi University of Medical Science, Yazd, Iran,   |c 2016-08-01T00:00:00Z. 
500 |a 1680-6433 
500 |a 2008-2177 
520 |a Background: With the prevalence of 6-10%, polycystic ovarian syndrome (PCOS) is considered the most common endocrinological disorder affecting women in their reproductive age. It has been suggested that genetic factors participate in the development of PCOS. Follicular development has been considered as one of the impaired processes in PCOS. Bone morphogenetic protein-15 (BMP-15) gene is a candidate gene in follicular development and its variants may play role in pathogenesis of PCOS. Objective: To investigate whether BMP-15 gene mutations are present in Iranian women with PCOS. Materials and Methods: In this cross-sectional study 5 ml venous blood samples was taken from 70 PCOS women referring to Afzalipour Hospital, Kerman University of Medical Sciences, Kerman, Iran, between January to December 2014. Genomic DNA was extracted from the blood sample by salting out method. Then a set of PCR reactions for exon1 of BMP-15 gene was performed using specific primers followed by genotyping with direct sequencing. Results: Two different polymorphisms were found in the gene under study. In total 20 patients (28.6%) were heterozygote (C/G), and 2 patients (2.86%) were homozygous (G/G) for c.-9C>G in 5´UTR promoter region of BMP-15 gene (rs3810682). In addition, in the coding region of exon1, three patients (4.3%) were heterozygote (G/A) for c.A308G (rs41308602). Two PCOS patients (2.86%) appeared to have both c.-9C>G (C/G) and c.A308G (G/A) variants simultaneously. Conclusion: Our research detected two polymorphisms of BMP-15 gene among PCOS patients, indicating that even though it cannot be concluded that variants of BMP-15 gene are the principal cause of polycystic ovarian syndrome; they could be involved in pathogenic process in development of PCOS. 
546 |a EN 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
690 |a Reproduction 
690 |a QH471-489 
655 7 |a article  |2 local 
786 0 |n Iranian Journal of Reproductive Medicine, Vol 14, Iss 8, Pp 527-532 (2016) 
787 0 |n http://www.ssu.ac.ir/ijrm/index.php/ijrm/article/view/2041/1013 
787 0 |n https://doaj.org/toc/1680-6433 
787 0 |n https://doaj.org/toc/2008-2177 
856 4 1 |u https://doaj.org/article/8ee0cda0b9ee4ef9af0f739a77eea0c9  |z Connect to this object online.