Publicação:
Relationship between oxidative stress, glutathione S-transferase polymorphisms and hydroxyurea treatment in sickle cell anemia

dc.contributor.authorHumberto Silva, Danilo Gruenig [UNESP]
dc.contributor.authorBelini Junior, Edis [UNESP]
dc.contributor.authorTorres, Lidiane de Souza [UNESP]
dc.contributor.authorRicci Junior, Octavio
dc.contributor.authorLobo, Clarisse de Castro
dc.contributor.authorBonini-Domingos, Claudia Regina [UNESP]
dc.contributor.authorde Almeida, Eduardo Alves [UNESP]
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.date.accessioned2014-05-20T14:03:10Z
dc.date.available2014-05-20T14:03:10Z
dc.date.issued2011-06-15
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.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.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.description.sponsorshipIdCNPq: 409691/2006-2
dc.description.sponsorshipIdFAPESP: 06/03873-1
dc.description.sponsorshipIdMinistry of Health: MS 3072/2007
dc.format.extent23-28
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.doi10.1016/j.bcmd.2011.03.004
dc.identifier.issn1079-9796
dc.identifier.lattes6713400866382255
dc.identifier.lattes3279428066176719
dc.identifier.orcid0000-0002-4603-9467
dc.identifier.urihttp://hdl.handle.net/11449/22258
dc.identifier.wosWOS:000291380400003
dc.language.isoeng
dc.publisherAcademic Press Inc. Elsevier B.V.
dc.relation.ispartofBlood Cells Molecules and Diseases
dc.relation.ispartofjcr1.836
dc.relation.ispartofsjr0,828
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderAcademic Press Inc. Elsevier B.V.
dspace.entity.typePublication
unesp.author.lattes6713400866382255
unesp.author.lattes3279428066176719[6]
unesp.author.orcid0000-0002-4603-9467[6]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências Letras e Ciências Exatas, São José do Rio Pretopt
unesp.departmentBiologia - IBILCEpt

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