The influence of hydroxyurea on oxidative stress in sickle cell anemia

OBJECTIVE: The oxidative stress in 20 sickle cell anemia patients taking hydroxyurea and 13 sickle cell anemia patients who did not take hydroxyurea was compared with a control group of 96 individuals without any hemoglobinopathy. METHODS: Oxidative stress was assessed by thiobarbituric acid reactiv...

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Main Authors: Lidiane de Souza Torres, Danilo Grünig Humberto da Silva, Edis Belini Junior, Eduardo Alves de Almeida, Clarisse Lopes de Castro Lobo, Rodolfo Delfini Cançado, Milton Artur Ruiz, Claudia Regina Bonini-Domingos
Format: Article
Language:English
Published: Elsevier 2012-01-01
Series:Revista Brasileira de Hematologia e Hemoterapia
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842012000600010
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spelling doaj-44f4c89b7eeb4f669650897092bdb8382020-11-25T01:36:29ZengElsevierRevista Brasileira de Hematologia e Hemoterapia1516-84841806-08702012-01-01346421425The influence of hydroxyurea on oxidative stress in sickle cell anemiaLidiane de Souza TorresDanilo Grünig Humberto da SilvaEdis Belini JuniorEduardo Alves de AlmeidaClarisse Lopes de Castro LoboRodolfo Delfini CançadoMilton Artur RuizClaudia Regina Bonini-DomingosOBJECTIVE: The oxidative stress in 20 sickle cell anemia patients taking hydroxyurea and 13 sickle cell anemia patients who did not take hydroxyurea was compared with a control group of 96 individuals without any hemoglobinopathy. METHODS: Oxidative stress was assessed by thiobarbituric acid reactive species production, the Trolox-equivalent antioxidant capacity and plasma glutathione levels. RESULTS: Thiobarbituric acid reactive species values were higher in patients without specific medication, followed by patients taking hydroxyurea and the Control Group (p < 0.0001). The antioxidant capacity was higher in patients taking hydroxyurea and lower in the Control Group (p = 0.0002 for Trolox-equivalent antioxidant capacity and p < 0.0292 for plasma glutathione). Thiobarbituric acid reactive species levels were correlated with higher hemoglobin S levels (r = 0.55; p = 0.0040) and lower hemoglobin F concentrations(r = -0.52; p = 0.0067). On the other hand, plasma glutathione levels were negatively correlated with hemoglobin S levels (r = -0.49; p = 0.0111) and positively associated with hemoglobin F values (r = 0.56; p = 0.0031). CONCLUSION: Sickle cell anemia patients have high oxidative stress and, conversely, increased antioxidant activity. The increase in hemoglobin F levels provided by hydroxyurea and its antioxidant action may explain the reduction in lipid peroxidation and increased antioxidant defenses in these individuals.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842012000600010HemoglobinopathiesOxidative stressAnemia, sickle cellHydroxyurea
collection DOAJ
language English
format Article
sources DOAJ
author Lidiane de Souza Torres
Danilo Grünig Humberto da Silva
Edis Belini Junior
Eduardo Alves de Almeida
Clarisse Lopes de Castro Lobo
Rodolfo Delfini Cançado
Milton Artur Ruiz
Claudia Regina Bonini-Domingos
spellingShingle Lidiane de Souza Torres
Danilo Grünig Humberto da Silva
Edis Belini Junior
Eduardo Alves de Almeida
Clarisse Lopes de Castro Lobo
Rodolfo Delfini Cançado
Milton Artur Ruiz
Claudia Regina Bonini-Domingos
The influence of hydroxyurea on oxidative stress in sickle cell anemia
Revista Brasileira de Hematologia e Hemoterapia
Hemoglobinopathies
Oxidative stress
Anemia, sickle cell
Hydroxyurea
author_facet Lidiane de Souza Torres
Danilo Grünig Humberto da Silva
Edis Belini Junior
Eduardo Alves de Almeida
Clarisse Lopes de Castro Lobo
Rodolfo Delfini Cançado
Milton Artur Ruiz
Claudia Regina Bonini-Domingos
author_sort Lidiane de Souza Torres
title The influence of hydroxyurea on oxidative stress in sickle cell anemia
title_short The influence of hydroxyurea on oxidative stress in sickle cell anemia
title_full The influence of hydroxyurea on oxidative stress in sickle cell anemia
title_fullStr The influence of hydroxyurea on oxidative stress in sickle cell anemia
title_full_unstemmed The influence of hydroxyurea on oxidative stress in sickle cell anemia
title_sort influence of hydroxyurea on oxidative stress in sickle cell anemia
publisher Elsevier
series Revista Brasileira de Hematologia e Hemoterapia
issn 1516-8484
1806-0870
publishDate 2012-01-01
description OBJECTIVE: The oxidative stress in 20 sickle cell anemia patients taking hydroxyurea and 13 sickle cell anemia patients who did not take hydroxyurea was compared with a control group of 96 individuals without any hemoglobinopathy. METHODS: Oxidative stress was assessed by thiobarbituric acid reactive species production, the Trolox-equivalent antioxidant capacity and plasma glutathione levels. RESULTS: Thiobarbituric acid reactive species values were higher in patients without specific medication, followed by patients taking hydroxyurea and the Control Group (p < 0.0001). The antioxidant capacity was higher in patients taking hydroxyurea and lower in the Control Group (p = 0.0002 for Trolox-equivalent antioxidant capacity and p < 0.0292 for plasma glutathione). Thiobarbituric acid reactive species levels were correlated with higher hemoglobin S levels (r = 0.55; p = 0.0040) and lower hemoglobin F concentrations(r = -0.52; p = 0.0067). On the other hand, plasma glutathione levels were negatively correlated with hemoglobin S levels (r = -0.49; p = 0.0111) and positively associated with hemoglobin F values (r = 0.56; p = 0.0031). CONCLUSION: Sickle cell anemia patients have high oxidative stress and, conversely, increased antioxidant activity. The increase in hemoglobin F levels provided by hydroxyurea and its antioxidant action may explain the reduction in lipid peroxidation and increased antioxidant defenses in these individuals.
topic Hemoglobinopathies
Oxidative stress
Anemia, sickle cell
Hydroxyurea
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842012000600010
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