Circulating inflammatory markers in polycystic ovary syndrome: a systematic review and metaanalysis

Fertil Steril. 2011 Mar 1;95(3):1048-58.e1-2. doi: 10.1016/j.fertnstert.2010.11.036. Epub 2010 Dec 17.

Abstract

Objective: To perform a review and metaanalysis of the studies evaluating the status of serum inflammatory markers in women with polycystic ovary syndrome (PCOS).

Design: Systematic review and metaanalysis of articles published in English before January 2010 and identified using the PubMed search engine.

Setting: Academic hospital.

Patient(s): Women with PCOS and appropriate controls.

Intervention(s): Measurement of serum concentrations of inflammatory markers by high-sensitivity techniques.

Main outcome measure(s): Metaanalyses of the mean difference in serum C-reactive protein (CRP), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) concentrations among patients with PCOS and appropriate controls, applying random-effects models to limit interstudy variability, and using appropriate estimates of evidence dissemination bias.

Result(s): Metaanalysis of the 31 articles meeting inclusion criteria showed that circulating CRP was 96% higher in women with PCOS compared to controls (95% confidence interval, 71%-122%; z = 7.32) without evidence of dissemination bias (Egger's regression intercept, 0.45; 95% confidence interval, -2.30 to 3.21). These findings persisted after excluding five studies with mismatches in body mass, frequency of obesity, or both, between women with PCOS and controls. Metaanalyses involving 10 studies of IL-6, and nine studies of TNF-α revealed no statistically significant differences between PCOS and controls.

Conclusion(s): Women with PCOS exhibit an elevation in circulating CRP that is independent of obesity. This finding corroborates existing molecular evidence of the chronic low-grade inflammation that may underpin the pathogenesis of this disorder.

Publication types

  • Meta-Analysis
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review
  • Systematic Review

MeSH terms

  • Biomarkers / blood*
  • Female
  • Glucose Intolerance / blood
  • Glucose Intolerance / immunology*
  • Humans
  • Inflammation / blood
  • Inflammation / immunology*
  • Obesity / blood
  • Obesity / immunology*
  • Polycystic Ovary Syndrome / blood
  • Polycystic Ovary Syndrome / immunology*

Substances

  • Biomarkers