Reactive oxygen species-induced oxidative stress in the development of insulin resistance and hyperandrogenism in polycystic ovary syndrome

J Clin Endocrinol Metab. 2006 Jan;91(1):336-40. doi: 10.1210/jc.2005-1696. Epub 2005 Oct 25.

Abstract

Context: Insulin resistance and chronic low level inflammation are often present in women with polycystic ovary syndrome (PCOS).

Objective: The purpose of this study was to determine the effects of hyperglycemia on reactive oxygen species (ROS) generation from mononuclear cells (MNCs) in PCOS.

Design: This was a prospective controlled study.

Setting: The study was conducted at an academic medical center.

Patients: The study population consisted of 16 women with PCOS (eight lean, eight obese) and 15 age- and body composition-matched controls (eight lean, seven obese).

Main outcome measures: Insulin sensitivity was derived from a 2-h, 75-g oral glucose tolerance test (IS(OGTT)). ROS generation and p47(phox) protein expression were quantitated from MNCs obtained from blood drawn fasting and 2 h after glucose ingestion.

Results: IS(OGTT) was lower in PCOS, compared with controls (3.1 +/- 0.3 vs. 6.3 +/- 0.9, P < 0.003). The percent change in ROS generation from MNCs was higher in lean and obese PCOS, compared with lean controls (138.8 +/- 21.3 and 154.2 +/- 49.1 vs. 0.6 +/- 12.7, P < 0.003). The percent change in ROS generation from MNCs correlated positively with glucose area under the curve (r = 0.38, P < 0.05), and plasma levels of testosterone (r = 0.59, P < 0.002) and androstenedione (r = 0.50, P < 0.009). The percent change in p47(phox) from MNCs was also higher in lean and obese PCOS, compared with lean controls (36.2 +/- 18.2 and 39.1 +/- 8.0 vs. -13.7 +/- 8.7, P < 0.02), and correlated negatively with IS(OGTT) (r = -0.39, P < 0.05).

Conclusion: ROS generation from MNCs in response to hyperglycemia is increased in PCOS independent of obesity. The resultant oxidative stress may contribute to a proinflammatory state that induces insulin resistance and hyperandrogenism in women with this disorder.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Androstenedione / blood
  • Area Under Curve
  • Body Composition / physiology
  • Body Weight / physiology
  • Female
  • Glucose / metabolism
  • Humans
  • Hyperandrogenism / metabolism*
  • Hyperglycemia / metabolism
  • Insulin Resistance / physiology*
  • Lipid Peroxidation / drug effects
  • Monocytes / metabolism
  • NADPH Oxidases
  • Obesity / metabolism
  • Oxidative Stress / physiology*
  • Phosphoproteins / biosynthesis
  • Polycystic Ovary Syndrome / metabolism*
  • Reactive Oxygen Species*
  • Testosterone / blood
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Waist-Hip Ratio

Substances

  • Phosphoproteins
  • Reactive Oxygen Species
  • Thiobarbituric Acid Reactive Substances
  • Testosterone
  • Androstenedione
  • NADPH Oxidases
  • neutrophil cytosolic factor 1
  • Glucose