Thrombomodulin and von Willebrand factor: relation to endothelial dysfunction and disease outcome in children with acute lymphoblastic leukemia.
| Title | Thrombomodulin and von Willebrand factor: relation to endothelial dysfunction and disease outcome in children with acute lymphoblastic leukemia. |
| Publication Type | Journal Article |
| Year of Publication | 2011 |
| Authors | Hatzipantelis, E. S., Athanassiou-Metaxa M., Gombakis N., Tzimouli V., Taparkou A., Sidi-Fragandrea V., Garipidou V., Papageorgiou T., Kleta D., Koliouskas D. E., & Athanasiadou-Piperopoulou F. |
| Journal | Acta Haematol |
| Volume | 125 |
| Issue | 3 |
| Pagination | 130-5 |
| Date Published | 2011 |
| ISSN | 1421-9662 |
| Keywords | Acute Disease, Adolescent, Biological Markers, Case-Control Studies, Child, Child, Preschool, Endothelium, Vascular, Female, Humans, Infant, Male, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Prognosis, Thrombomodulin, Treatment Outcome, von Willebrand Factor |
| Abstract | The severe endothelial dysfunction in children with acute lymphoblastic leukemia (ALL) can result from the disease itself, from treatment, or from other conditions (e.g. sepsis). The aim of this study was to determine the levels of markers of endothelial activation in children with ALL and to assess their potential prognostic value. Fifty-two children with ALL, 19 children with ALL 1-10 years after the completion of therapy, and 28 healthy children were studied. In children with ALL, there was a significant increase in thrombomodulin (TM) and von Willebrand factor (vWF) levels during the acute phase of the disease and during treatment. Children with an unfavorable outcome had higher levels of TM. In conclusion, severe endothelial dysfunction is present during the acute phase of ALL and during treatment and appears to result from the disease itself. Serum TM and vWF levels might represent additional, but not independent, prognostic markers in childhood ALL. |
| DOI | 10.1159/000322120 |
| Alternate Journal | Acta Haematol. |
| PubMed ID | 21150180 |
