Clinical and biochemical presentations of polycystic ovary syndrome among obese and nonobese women

Fertil Steril. 2009 Dec;92(6):1960-5. doi: 10.1016/j.fertnstert.2008.09.003. Epub 2008 Nov 5.

Abstract

Objective: To study the differences in clinical and biochemical characteristics between obese and nonobese women with polycystic ovary syndrome (PCOS).

Design: Retrospective study.

Setting: University teaching hospital.

Patient(s): Four hundred sixty-four Taiwan Chinese women, among whom 295 were diagnosed with PCOS and 169 were non-PCOS controls.

Main outcome measure(s): Body mass index, average menstrual interval, modified Ferriman-Gallwey score, acne, total T, and waist-to-hip ratio.

Result(s): Obese women with polycystic ovary morphology (PCOM) had a greater risk of developing of PCOS (odds ratio [OR], 2.5; 95% confidence interval [CI], 1.5-10.4) than nonobese women with PCOM. Obese women with PCOM had a higher incidence oligomenorrhea (OR, 2.6; 95% CI, 1.6-4.1) and biochemical hyperandrogenemia (OR, 2.5; 95% CI, 1.6-4.0) than nonobese women with PCOM. Obese subjects with PCOS had a higher risk of developing oligomenorrhea (OR, 2.2; 95% CI, 1.3-3.7) and biochemical hyperandrogenemia (OR, 2.6; 95% CI, 1.6-4.2) than nonobese women with PCOS. Moreover, obese women with PCOS had significantly higher serum total T levels and more prolonged menstrual intervals than nonobese women with PCOS. Notably, the obese women with PCOS presented less acne than the nonobese subjects (OR, 0.5; 95% CI, 0.3-0.9).

Conclusion(s): Obese women with PCOS had more severe ovulatory dysfunction and higher serum total T levels than nonobese subjects. Moreover, obese women with PCOS had a significantly lower frequency of acne than nonobese subjects.

Publication types

  • Comparative Study

MeSH terms

  • Acne Vulgaris / epidemiology
  • Adolescent
  • Adult
  • Body Mass Index*
  • Female
  • Follicle Stimulating Hormone / blood
  • Hirsutism / epidemiology
  • Humans
  • Hyperandrogenism / epidemiology
  • Incidence
  • Luteinizing Hormone / blood
  • Menstruation
  • Obesity / epidemiology*
  • Oligomenorrhea / epidemiology
  • Polycystic Ovary Syndrome / blood
  • Polycystic Ovary Syndrome / epidemiology*
  • Polycystic Ovary Syndrome / physiopathology*
  • Prolactin / blood
  • Risk Factors
  • Taiwan / epidemiology
  • Testosterone / blood
  • Young Adult

Substances

  • Testosterone
  • Prolactin
  • Luteinizing Hormone
  • Follicle Stimulating Hormone