The CD105:CD106 microparticle ratio is CD106 dominant in polycystic ovary syndrome compared to type 2 diabetes and healthy subjects

Endocrine. 2019 Nov;66(2):220-225. doi: 10.1007/s12020-019-02059-9. Epub 2019 Aug 27.

Abstract

Background: A retrospective analysis was carried out from patients and controls during the past 5 years from a series of studies investigating endothelial microparticles (MP).

Methods: In total, 319 samples from 207 individuals were included in this analysis, from patients with type 2 diabetes (T2D, n = 105), women with polycystic ovary syndrome (PCOS, n = 145) and healthy volunteers (n = 69). All data were generated via the same flow cytometry protocol with the same antibody clones. Endothelial markers CD105 (Endoglin) and CD106 (Vascular cell adhesion molecule-1) were used to enumerate MP in venous blood.

Results: The ratio of CD105MP:CD106MP was significantly different between groups (F = 63.43, p < 0.0001). Women with PCOS were found to have a median CD105MP:CD106MP ratio of 0.40 (IQR 0.24-0.57), suggesting approximately two CD106MP were found per CD105MP. The T2D group showed a median ratio of 2.32 (1.51-3.69) whereas in healthy volunteers the ratio was 2.21 (1.63-3.55). Serum intercellular adhesion molecule-1 was also shown to be significantly increased in PCOS when compared with control or T2D groups (F = 14.5, p < 0.001).

Conclusion: These data suggest that women with PCOS have an altered endothelial MP release in favour of CD106. Thus a potential activated endothelial state exists in women with PCOS with a shift towards a predominantly CD106MP profile.

Keywords: Endothelial microparticles; Polycystic ovary syndrome; VCAM-1.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Biomarkers / blood
  • Cell-Derived Microparticles / metabolism*
  • Diabetes Mellitus, Type 2 / metabolism*
  • Endoglin / metabolism*
  • Female
  • Humans
  • Intercellular Adhesion Molecule-1 / blood
  • Polycystic Ovary Syndrome / metabolism*
  • Retrospective Studies
  • Risk Factors
  • Vascular Cell Adhesion Molecule-1 / metabolism*
  • Young Adult

Substances

  • Biomarkers
  • Endoglin
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1