Impact of Continuous Estroprogestin Treatment on Circulating Microparticle Levels in Deep Endometriosis Patients

Int J Mol Sci. 2023 Jul 22;24(14):11802. doi: 10.3390/ijms241411802.

Abstract

There has been increasing interest in the study of new pathogenic mechanisms in endometriosis (END), including the coagulation/fibrinolysis system and its link with inflammation and tissue remodeling. It has been suggested that END patients, especially with deep-infiltrating (DE) forms, could present a hypercoagulable state revealing higher levels of proinflammatory and procoagulant markers, such as total circulating microparticles (cMPs) and cMP-TF (tissue factor), released by cells in response to damage, activation, or apoptosis. However, no previous study has assessed the effect of END hormonal treatments on cMP and cMP-TF levels. Therefore, the aim of this study was to evaluate the impact of these treatments on cMP and cMP-TF levels in DE patients. Three groups were compared: DE patients receiving a continuous combined oral contraceptive regimen (CCOCR) (n = 41), DE patients without CCOCR (n = 45), and a control group (n = 43). cMP and cMP-TF levels were evaluated in platelet-free plasma. A significant decrease in the total cMP levels was found in the DE group with CCOCR versus the group without CCOCR, reflecting a higher chronic inflammatory status in DE patients that decreased with the treatment. cMP-TF levels were higher in DE patients receiving CCOCR versus those not receiving CCOCR, suggesting that treatments containing estrogens play a predominant role in suppressing the inhibitory pathway of TF.

Keywords: circulating microparticles; coagulation; combined oral contraceptives; endometriosis; estroprogestin treatment; hormonal therapy; tissue factor.

MeSH terms

  • Blood Coagulation
  • Cell-Derived Microparticles* / metabolism
  • Endometriosis* / pathology
  • Ethinyl Estradiol
  • Female
  • Humans
  • Inflammation / metabolism
  • Norpregnenes / metabolism
  • Thromboplastin / metabolism

Substances

  • estroprogestin
  • Ethinyl Estradiol
  • Norpregnenes
  • Thromboplastin