Abstract | OBJECTIVE: METHODS: Fifty adult sickle cell anemia patients were included in the study. All patients were taking hydroxyurea for at least six months and were followed at the outpatient clinic of a hospital in Fortaleza, Ceará, Brazil. The control group consisted of 20 hemoglobin AA individuals. The reticulocyte count was performed by an automated methodology, lactate dehydrogenase and uric acid were measured by spectrophotometry and arginase I by enzyme-linked immunosorbent assay (ELISA). The presence of Hb S was detected by high-performance liquid chromatography. The level of significance was set for a p-value <0.05. RESULTS: CONCLUSION:
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Authors | Juliane Almeida Moreira, Marília Rocha Laurentino, Rosângela Pinheiro Gonçalves Machado, Maritza Cavalcante Barbosa, Ronaldo Pinheiro Gonçalves, Amanda de Menezes Mota, Lilianne Brito da Silva Rocha, Alice Maria Costa Martins, Alcínia Braga de Lima Arruda, Iêda Pereira de Souza, Romélia Pinheiro Gonçalves |
Journal | Revista brasileira de hematologia e hemoterapia
(Rev Bras Hematol Hemoter)
2015 May-Jun
Vol. 37
Issue 3
Pg. 167-71
ISSN: 1516-8484 [Print] Brazil |
PMID | 26041418
(Publication Type: Journal Article)
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Copyright | Copyright © 2015 Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier Editora Ltda. All rights reserved. |