Pentraxin 3 as a marker of endothelial dysfunction in young women with polycystic ovary syndrome (PCOS)

Scand J Clin Lab Invest. 2019 Oct;79(6):419-423. doi: 10.1080/00365513.2019.1637535. Epub 2019 Jul 7.

Abstract

One of the consequences of polycystic ovary syndrome (PCOS) is an increased risk of early development of cardiovascular diseases. Pentraxin-3 (PTX-3) is a new potential marker of endothelial dysfunction. The aim of the study was to assess PTX3 and other markers of endothelial dysfunction in PCOS women. The study enrolled 99 stable body mass PCOS women (17 normal weight, 21 overweight and 61 obese). Anthropometric measurements and serum/plasma levels of glucose, insulin, lipids, estradiol, testosterone, sex hormone binding globulin, 17-OH progesterone, free androgen index, pentraxin-3 (PTX3), soluble intercellular (sICAM-1) and vascular cell adhesion molecule 1 (sVCAM-1), endothelin-1 and total nitric oxide metabolites (tNO) concentrations were assessed. Groups were divided into tercile-subgroups according to PTX3 serum levels. Serum PTX3 tercile-subgroups significantly differed in respect to tNO, endothelin-1 and sVCAM-1, but not sICAM-1. The levels of tNO, endothelin-1 and sVCAM-1 were significantly decreased in the subgroup with the lowest PTX3 levels compared to both middle (tNO and endothelin 1) and upper tercile subgroups (all of them). There were significant positive correlations between log10(PTX3) and log10(tNO) (r = 0.34, p < .001), log10(endothelin-1) (r = 0.41, p < .001) as well as sVCAM-1 levels (r = 0.22, p < .05). Circulating PTX-3 levels seem to be a marker of endothelial dysfunction in PCOS women.

Keywords: Endothelium dysfunction; PCOS; PTX-3; adhesion molecules; nitric oxide metabolites.

MeSH terms

  • Adult
  • Biomarkers / blood
  • C-Reactive Protein / metabolism*
  • Cross-Sectional Studies
  • Endothelium, Vascular / pathology*
  • Female
  • Humans
  • Nitric Oxide / blood
  • Nitric Oxide / metabolism
  • Polycystic Ovary Syndrome / blood*
  • Serum Amyloid P-Component / metabolism*
  • Vascular Cell Adhesion Molecule-1 / blood

Substances

  • Biomarkers
  • Serum Amyloid P-Component
  • Vascular Cell Adhesion Molecule-1
  • PTX3 protein
  • Nitric Oxide
  • C-Reactive Protein