Normalized coagulation markers and anticoagulation proteins in children with severe β-thalassemia disease after stem cell transplantation

Thromb Res. 2012 Jun;129(6):765-70. doi: 10.1016/j.thromres.2011.07.046. Epub 2011 Sep 8.

Abstract

The hypercoagulable state is well recognized in patients with severe β-thalassemia disease. One of the mechanisms of chronic hypercoagulable state is the abnormal expression of phosphatidylserine on red blood cells (RBC). This study aimed to determine the coagulable state in patients with severe β-thalassemia disease following successful stem cell transplantation (SCT). Subjects were classified into three groups: normal controls (NC), β-thalassemia disease receiving regular transfusion (Thal-RT) and β-thalassemia disease post SCT (Thal-SCT). Sixty eight subjects, aged 3-17years, consisting of 21 NC, 28 Thal-RT and 19 Thal-SCT were enrolled. After SCT, the annexin V level in Thal-SCT was normalized. At the median follow-up time of 70.3 (50.9-84.2) months after SCT, the levels of coagulation markers (thrombin antithrombin complex, prothrombin fragment and D-dimer) and anticoagulation proteins (protein C, S and antithrombin activities) returned to the levels similar to controls.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood
  • Blood Coagulation / physiology*
  • Blood Coagulation Tests
  • Blood Proteins / analysis
  • Blood Proteins / metabolism
  • Child
  • Female
  • Humans
  • Male
  • Stem Cell Transplantation / methods*
  • beta-Thalassemia / blood*
  • beta-Thalassemia / surgery

Substances

  • Biomarkers
  • Blood Proteins