| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2006;37:1424.)
© 2006 American Heart Association, Inc.
Original Contributions |
From the Department of Neurology, Stroke Research Program, Department of Neurology School of Medicine, Medical College of Georgia, Augusta, GA (N.E.L., N.O., R.J.A.); the Department of Medicine and Sickle Cell Center (A.K.), Medical College of Georgia, Augusta, GA; and the New England Research Institutes (D.B.), Watertown, MA.
Correspondence to Robert Adams, MD, Department of Neurology, Stroke Research Program, Department of Neurology, School of Medicine, Medical College of Georgia, 1429 Harper St, Rm HF 1154, Augusta, GA 30912. E-mail rjadams{at}mail.mcg.edu
Background and Purpose Intravascular hemolysis releases large amounts of free hemoglobin (PFH) in plasma of sickle- cell disease (SCD) patients. PFH has been associated with harmful endothelial actions including scavenging nitric oxide (NO). Whether PFH plays a role in stroke in SCD has not been examined.
Methods Serum levels of PFH, lactate dehydrogenase, and total bilirubin were measured in stored sera from children at risk for stroke treated in a randomized controlled trial of regular red cell transfusion (STOP study). Baseline and post-treatment (
1 year of transfusion) were compared to determine whether treatment (which reduces stroke risk by 90%) was associated with reduction in markers of hemolysis.
Results Baseline serum PFH values did not differ between treatment groups. PFH declined with repeated transfusion from 78.7±8.2 mg/dL to 34.4±3.4 mg/dL (P<0.001). With only episodic or no transfusion the drop was smaller: 80.9±7.5 to 62.8±5.0 (P=0.019). The decrease was larger in those with regular transfusion (56% versus 22%; P<0.001). Reduction of lactate dehydrogenase and total bilirubin was observed only in those on regular transfusion.
Conclusions Regular transfusion which lowers stroke risk is associated with a significant reduction in PFH. A role for PFH in promoting stroke in SCD should be investigated.
Key Words: children hemolysis stroke
This article has been cited by other articles:
![]() |
R. I. Liem, L. T. Young, and A. A. Thompson Tricuspid regurgitant jet velocity is associated with hemolysis in children and young adults with sickle cell disease evaluated for pulmonary hypertension Haematologica, November 1, 2007; 92(11): 1549 - 1552. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Sebastiani, V. G. Nolan, C. T. Baldwin, M. M. Abad-Grau, L. Wang, A. H. Adewoye, L. C. McMahon, L. A. Farrer, J. G. Taylor IV, G. J. Kato, et al. A network model to predict the risk of death in sickle cell disease Blood, October 1, 2007; 110(7): 2727 - 2735. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. A. Zimmerman, W. H. Schultz, S. Burgett, N. A. Mortier, and R. E. Ware Hydroxyurea therapy lowers transcranial Doppler flow velocities in children with sickle cell anemia Blood, August 1, 2007; 110(3): 1043 - 1047. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. R. DeBaun and J. J. Field Limitations of Clinical Trials in Sickle Cell Disease: A Case Study of the Multi-center Study of Hydroxyurea (MSH) Trial and the Stroke Prevention (STOP) Trial Hematology, January 1, 2007; 2007(1): 482 - 488. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. S. Platt Prevention and Management of Stroke in Sickle Cell Anemia Hematology, January 1, 2006; 2006(1): 54 - 57. [Abstract] [Full Text] [PDF] |
||||
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2006 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |