Association of Gly972Arg variant of insulin receptor substrate-1 with metabolic features in women with polycystic ovary syndrome

Fertil Steril. 2005 Aug;84(2):407-12. doi: 10.1016/j.fertnstert.2005.01.133.

Abstract

Objective: To examine the prevalence and the effects of Gly972Arg (G972A) variant of insulin receptor substrate-1 (IRS-1) in women with polycystic ovary syndrome (PCOS).

Design: Controlled clinical study.

Setting: An academic clinical research center.

Patient(s): Sixty women with PCOS and 60 control women matched for age.

Intervention(s): Biometric measures, metabolic and hormonal measures, genetic analyses.

Main outcome measure(s): Serum androgens, glucose, and insulin were measured. Blood leukocytes were used for genetic analyses.

Result(s): The G972A variant was encountered more often in women with PCOS. The G972A carriers were more obese than their counterparts, had higher fasting insulin levels, and were more insulin-resistant. However, androgen levels did not differ on the basis of IRS-1 genotype.

Conclusion(s): We observed that the G972A variant of IRS-1 was more prevalent in women with PCOS, and that it had important metabolic effects without having a direct effect on the androgen levels. However, the G972A variant of IRS-1 may modulate reproduction by lowering sex hormone-binding globulin in both healthy women and women with PCOS.

Publication types

  • Controlled Clinical Trial

MeSH terms

  • Analysis of Variance
  • Arginine / genetics*
  • Blood Glucose / genetics*
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / genetics
  • Female
  • Genetic Variation / genetics*
  • Glycine / genetics*
  • Humans
  • Insulin / blood
  • Insulin / genetics*
  • Insulin Receptor Substrate Proteins
  • Phosphoproteins / genetics*
  • Polycystic Ovary Syndrome / blood
  • Polycystic Ovary Syndrome / genetics*

Substances

  • Blood Glucose
  • IRS1 protein, human
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Phosphoproteins
  • Arginine
  • Glycine