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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/22258
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dc.contributor.authorHumberto Silva, Danilo Gruenig-
dc.contributor.authorBelini Junior, Edis-
dc.contributor.authorTorres, Lidiane de Souza-
dc.contributor.authorRicci Junior, Octavio-
dc.contributor.authorLobo, Clarisse de Castro-
dc.contributor.authorBonini-Domingos, Claudia Regina-
dc.contributor.authorde Almeida, Eduardo Alves-
dc.date.accessioned2014-05-20T14:03:10Z-
dc.date.accessioned2016-10-25T17:09:31Z-
dc.date.available2014-05-20T14:03:10Z-
dc.date.available2016-10-25T17:09:31Z-
dc.date.issued2011-06-15-
dc.identifierhttp://dx.doi.org/10.1016/j.bcmd.2011.03.004-
dc.identifier.citationBlood Cells Molecules and Diseases. San Diego: Academic Press Inc. Elsevier B.V., v. 47, n. 1, p. 23-28, 2011.-
dc.identifier.issn1079-9796-
dc.identifier.urihttp://hdl.handle.net/11449/22258-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/22258-
dc.description.abstractThis study evaluated the oxidative stress and antioxidant capacity markers in sickle cell anemia (SCA) patients with and without treatment with hydroxyurea. We assessed GSTT1, GSTM1 and GSTP1 polymorphisms in patients and a control group. The study groups were composed of 48 subjects without hemoglobinopathies and 28 SCA patients, 13 treated with HU [SCA (+ HU)], and 15 SCA patients not treated with HU [SCA (- HU)]. We observed a significant difference for GSTP1 polymorphisms in SCA patients with the V/V genotype that showed higher glutathione (GSH) and Trolox equivalent antioxidant capacity (TEAC) (p = 0.0445 and p = 0.0360), respectively, compared with the I/I genotype. HU use was associated with a 35.2% decrease in the lipid peroxidation levels of the SCA (+ HU) group (p<0.0001). Moreover, the SCA (+ HU) group showed higher TEAC as compared to the control group (p = 0.002). We did not find any significant difference in glutathione-S-transferase (GST) activity between the groups (p = 0.76), but the catalase (CAT) activity was about 17% and 30% decreased in the SCA (+ HU) and SCA (HU) groups, respectively (p<0.00001). Whereas the plasma GSH levels were similar to 2 times higher in the SCA patients than the control group (p = 0.0005). HU use has contributed to higher CAT activity and TEAC, and lower lipid peroxidation in patients under treatment. These findings may explain the influence of HU in ameliorating oxidative stress on SCA subjects. (C) 2011 Elsevier B.V. All rights reserved.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.description.sponsorshipMinistry of Health-
dc.format.extent23-28-
dc.language.isoeng-
dc.publisherAcademic Press Inc. Elsevier B.V.-
dc.sourceWeb of Science-
dc.subjectSickle cell anemiaen
dc.subjectOxidative stressen
dc.subjectHydroxyureaen
dc.subjectGST polymorphismsen
dc.titleRelationship between oxidative stress, glutathione S-transferase polymorphisms and hydroxyurea treatment in sickle cell anemiaen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionFaculdade de Medicina de São José do Rio Preto (FAMERP)-
dc.contributor.institutionHematol State Inst Arthur de Siqueira Cavalcanti-
dc.description.affiliationUNESP São Paulo State Univ, Dept Biol, Hemoglobin & Hematol Genet Dis Lab, São Paulo, Brazil-
dc.description.affiliationSao Jose do Rio Preto Med Sch FAMERP, Dept Med, São Paulo, Brazil-
dc.description.affiliationHematol State Inst Arthur de Siqueira Cavalcanti, Rio de Janeiro, Brazil-
dc.description.affiliationUNESP São Paulo State Univ, Dept Chem & Environm Sci, São Paulo, Brazil-
dc.description.affiliationUnespUNESP São Paulo State Univ, Dept Biol, Hemoglobin & Hematol Genet Dis Lab, São Paulo, Brazil-
dc.description.affiliationUnespUNESP São Paulo State Univ, Dept Chem & Environm Sci, São Paulo, Brazil-
dc.description.sponsorshipIdCNPq: 409691/2006-2-
dc.description.sponsorshipIdFAPESP: 06/03873-1-
dc.description.sponsorshipIdMinistry of Health: MS 3072/2007-
dc.identifier.doi10.1016/j.bcmd.2011.03.004-
dc.identifier.wosWOS:000291380400003-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofBlood Cells Molecules and Diseases-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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