Increased procoagulant cell-derived microparticles (C-MP) in splenectomized patients with ITP

V Fontana1, W Jy, E R Ahn

  • 1Wallace H Coulter Platelet Laboratory, Division of Hematology/Oncology, University of Miami, Miller School of Medicine, 1600 NW 10th Ave, Room 7109A, Miami, FL 33136, USA.

Thrombosis Research
|March 13, 2008
PubMed
Abstract

Insights

Splenectomy increases cell-derived microparticles (C-MP), particularly red cell-derived (RMP) and leukocyte-derived (LMP), potentially raising thrombosis and cardiovascular disease risks. The spleen likely clears these procoagulant C-MP.

Area of Science:

  • Hematology
  • Immunology
  • Vascular Biology

Background:

  • Splenectomy is a common procedure with incompletely understood long-term safety.
  • While infection risk is known, thrombosis and cardiovascular disease risks post-splenectomy require further elucidation.

Purpose of the Study:

  • To investigate levels of cell-derived microparticles (C-MP) in splenectomized versus non-splenectomized patients with immune thrombocytopenia (ITP).
  • To explore the association between C-MP levels, coagulation parameters, and potential long-term risks following splenectomy.

Main Methods:

  • Assessed levels of platelet-derived (PMP), leukocyte-derived (LMP), red cell-derived (RMP), and endothelial cell-derived (EMP) microparticles via flow cytometry.
  • Measured coagulation parameters including PT, aPTT, and FVIII, IX, XI activities.
  • Compared these measures between 23 splenectomized ITP (ITP-S) and 53 non-splenectomized ITP (ITP-nS) patients.

Main Results:

  • Significantly elevated RMP (p=0.0035) and LMP (p<0.0001) were observed in ITP-S patients compared to ITP-nS.
  • ITP-S patients exhibited significantly shorter aPTT (p=0.029).
  • RMP correlated with shorter aPTT and increased activities of factors VIII, IX, and XI.

Conclusions:

  • Splenectomy is associated with elevated RMP and LMP, suggesting the spleen's role in clearing procoagulant C-MP.
  • Increased C-MP levels post-splenectomy may contribute to heightened risks of thrombosis, atherosclerosis, and cardiovascular disease.