(2015) Association study of calpain-10 gene polymorphism in patients with polycystic ovarian syndrome. Genetics in the Third Millennium. pp. 3924-3930.
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Abstract
Polycystic Ovarian syndrome (PCOS) is a common endocrine disorder with a global prevalence of 5-10 among women of reproductive age. PCOS is characterized by chronic anovulation, polycystic ovaries, hyperandrogenism, hirsutism, overweight, insulin resistance, and infertility. It is well-known that PCOS is a complex trait similar to type-2 diabetes in which both genetic and environmental factors play a crucial role in the pathogenesis of the disease. A couple of type-2 diabetes susceptibility genes including those for insulin secretion and action such as Calpain-10 have shown considerable contribution to genetic predisposition to PCOS. Since Calpain-10 gene seems to be a strong candidate gene for PCOS, we aimed to investigate the role of Caplain-10 gene polymorphism UCSNP-44 (T/C) located in a transcription enhancer element of the gene in disease susceptibility. We carried out a cross-sectional case-control study. Using simple random sampling, ninety healthy women were selected. All ninety patients fulfilled the 2003 Rotterdam criteria of PCOS. The subjects were genotyped for Caplain-10 gene polymorphism UCSNP-44 (T/C) using PCR-RFLP. Differences in genotype distributions between case and control subjects were examined via the chi-square test. Although PCOS showed a high prevalence among women in Bandar Abbas, Caplain-10 gene polymorphism UCSNP-44 (T/C) UCSNP44 did not influence the susceptibility to PCOS. © 2015, Iranian Neurogenetics Society. All rights reserved.
Item Type: | Article |
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Keywords: | calpain 10; follitropin; genomic DNA; luteinizing hormone; prolactin; thyrotropin, acne; adult; allele; Article; calpain 10 gene; chromosome 2q; controlled study; DNA extraction; DNA polymorphism; exon; female; galactorrhea; gene; gene frequency; genetic association; genetic predisposition; genotype; hirsutism; human; hypertension; major clinical study; menstrual irregularity; non insulin dependent diabetes mellitus; obesity; ovary polycystic disease; single nucleotide polymorphism |
Page Range: | pp. 3924-3930 |
Journal or Publication Title: | Genetics in the Third Millennium |
Volume: | 13 |
Number: | 1 |
Publisher: | Iranian Neurogenetics Society |
Depositing User: | ms soheila Bazm |
URI: | http://eprints.ssu.ac.ir/id/eprint/9412 |
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