1. Normalized coagulation markers and anticoagulation proteins in children with severe β-thalassemia disease after stem cell transplantation
- Author
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Somtawin Sirireung, Arjit Tirakanjana, Nongnuch Sirachainan, Ampaiwan Chuansumrit, Jaruwan Thongsad, Suradej Hongeng, Samart Pakakasama, Praguywan Kadegasem, and Napaporn Archararit
- Subjects
Male ,medicine.medical_specialty ,Thalassemia ,Gastroenterology ,chemistry.chemical_compound ,immune system diseases ,Annexin ,hemic and lymphatic diseases ,Internal medicine ,medicine ,Humans ,Child ,Blood Coagulation ,business.industry ,beta-Thalassemia ,Antithrombin ,Blood Proteins ,Hematology ,Phosphatidylserine ,medicine.disease ,Transplantation ,surgical procedures, operative ,Coagulation ,chemistry ,Immunology ,Female ,Blood Coagulation Tests ,Stem cell ,business ,Biomarkers ,Protein C ,Stem Cell Transplantation ,medicine.drug - 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 3–17 years, 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.
- Published
- 2012
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