Increased insulin-like growth factor-1 in relation to cardiovascular function in polycystic ovary syndrome: friend or foe?

Gynecol Endocrinol. 2015 Oct;31(10):801-7. doi: 10.3109/09513590.2015.1075497. Epub 2015 Aug 18.

Abstract

The incidence of cardiovascular disease (CVD) in patients with polycystic ovary syndrome (PCOS) is very high and conventional risk factors only partially explain excessive risk of developing CVD in patients of PCOS. The pathophysiology of PCOS is very unique, and several hormonal and metabolic changes occur. Several observations suggest that serum IGF-1 levels decrease in insulin resistance, which results in IGF-1 deficiency. In patient of PCOS, close relationships have been demonstrated between insulin resistance and serum IGF-1 levels. Hyperinsulinemic insulin resistance results in a general augmentation of steroidogenesis and LH release in PCOS. The action of IGF-1 varies in different tissues possibly via autocrine or paracrine mechanisms. The increase or decrease in IGF-1 in different tissues results in differential outcomes. Several studies suggest that lowered circulating IGF-1 levels play important role in the initiation of the cardiac hypertrophic response which results in the risk of cardiovascular disease. While recent results suggests that individual with elevated IGF-1 is protected against cardiovascular disease. Thus IGF-1 shows versatile pleiotropic actions. This review provides a current perspective on increased level of IGF-1 in PCOS and also adds to the current controversy regarding the roles of IGF-1 in cardiovascular disease.

Keywords: Cardiovascular disease; hyperinsulinemia; insulin like growth factor-1; polycystic ovary syndrome.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cardiovascular System / physiopathology*
  • Female
  • Humans
  • Insulin / blood
  • Insulin Resistance
  • Insulin-Like Growth Factor I / metabolism*
  • Luteinizing Hormone / blood
  • Polycystic Ovary Syndrome / blood*
  • Polycystic Ovary Syndrome / physiopathology

Substances

  • Insulin
  • Insulin-Like Growth Factor I
  • Luteinizing Hormone