A novel single nucleotide polymorphism of INSR gene for polycystic ovary syndrome

Fertil Steril. 2008 May;89(5):1213-1220. doi: 10.1016/j.fertnstert.2007.05.026. Epub 2007 Jul 20.

Abstract

Objective: To investigate several single nucleotide polymorphisms (SNPs) in the insulin receptor (INSR) gene that have significant associations with pathogenesis of polycystic ovary syndrome (PCOS) in a Korean population.

Design: Case-control study.

Setting: University-based hospital.

Patient(s): 134 patients with PCOS and 100 healthy women as controls.

Intervention(s): All exons of INSR in DNA samples from 100 healthy women and 134 women with PCOS were sequenced and compared.

Main outcome measure(s): Frequencies of genotypes for several SNPs in INSR gene that were found as specifically expressed SNPs in a Korean population.

Result(s): Among nine SNPs analyzed in a large population, the genotypic frequencies of eight SNPs were similar, and they had no statistically significant association with PCOS. However, the frequency of a minor allele for one novel SNP, +176477 C>T, was higher in the control group than the patient group.

Conclusion(s): Among the analyzed SNPs, +176477 C>T, a novel SNP in the INSR gene, was associated with the pathogenesis of PCOS in a Korean population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / genetics*
  • Asian People / genetics
  • Case-Control Studies
  • Chromosomes, Human, Pair 19 / genetics
  • Female
  • Gene Frequency / genetics
  • Genotype
  • Haplotypes / genetics
  • Humans
  • Korea
  • Polycystic Ovary Syndrome / ethnology
  • Polycystic Ovary Syndrome / genetics*
  • Polymorphism, Single Nucleotide / genetics*
  • Receptor, Insulin / genetics*
  • Signal Transduction / genetics

Substances

  • Antigens, CD
  • INSR protein, human
  • Receptor, Insulin