Single nucleotide polymorphism in exon 17 of the insulin receptor gene is not associated with polycystic ovary syndrome in a Korean population

Fertil Steril. 2006 Aug;86(2):380-4. doi: 10.1016/j.fertnstert.2005.12.073. Epub 2006 Jun 27.

Abstract

Objective: To assess the association between the single nucleotide polymorphism of the insulin receptor (INSR) gene and polycystic ovary syndrome (PCOS) in a Korean population.

Design: Case-control study.

Setting: University-based hospital.

Patient(s): One hundred seventy-four patients with PCOS and 93 healthy women as controls.

Main outcome measure(s): Frequency of three genotypes for single nucleotide polymorphism found in exon 17 of INSR gene.

Result(s): The high frequency of the T allele was shown both in patient and control groups. The frequency of C allele, which known as a normal allele, was slightly higher in the patient group than in the control group.

Conclusion(s): The C/T polymorphism in exon 17 of the INSR gene is not associated with susceptibility of PCOS in a Korean population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Asian People / genetics*
  • Case-Control Studies
  • Cytosine
  • Exons*
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Middle Aged
  • Molecular Sequence Data
  • Polycystic Ovary Syndrome / genetics*
  • Polymorphism, Restriction Fragment Length
  • Polymorphism, Single Nucleotide*
  • Receptor, Insulin / genetics*
  • Thymine

Substances

  • Cytosine
  • Receptor, Insulin
  • Thymine

Associated data

  • RefSeq/NM_000208