Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia

Detalhes bibliográficos
Autor(a) principal: Yahouédéhou, Sètondji Cocou Modeste Alexandre
Data de Publicação: 2019
Outros Autores: Guarda, Caroline Conceição da, Figueiredo, Camylla Vilas Boas, Santiago, Rayra Pereira, Carvalho, Suellen Pinheiro, Fiuza, Luciana Magalhães, Ndidi, Uche Samuel, Oliveira, Rodrigo Mota, Carvalho, Magda Oliveira Seixas, Nascimento, Valma Maria Lopes, Rocha, Larissa Carneiro, Lyra, Isa Menezes, Adorno, Elisângela Vitória, Goncalves, Marilda Souza
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da FIOCRUZ (ARCA)
Texto Completo: https://www.arca.fiocruz.br/handle/icict/34775
Resumo: 1- Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (470959/2014-2 and 405595/2016-6 to MSG). http://www.cnpq.br/and 2- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001 to SCMAY, RPS, and SPC.
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spelling Yahouédéhou, Sètondji Cocou Modeste AlexandreGuarda, Caroline Conceição daFigueiredo, Camylla Vilas BoasSantiago, Rayra PereiraCarvalho, Suellen PinheiroFiuza, Luciana MagalhãesNdidi, Uche SamuelOliveira, Rodrigo MotaCarvalho, Magda Oliveira SeixasNascimento, Valma Maria LopesRocha, Larissa CarneiroLyra, Isa MenezesAdorno, Elisângela VitóriaGoncalves, Marilda Souza2019-08-13T16:32:26Z2019-08-13T16:32:26Z2019YAHOUÉDÉHOU, Sètondji Cocou Modeste Alexandre et al. Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia. Plos One, v. 14, n. 7, p. 1-13, 2019.1932-6203https://www.arca.fiocruz.br/handle/icict/3477510.1371/journal.pone.02180401- Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (470959/2014-2 and 405595/2016-6 to MSG). http://www.cnpq.br/and 2- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001 to SCMAY, RPS, and SPC.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.Ahmadu Bello University. Department of Biochemistry. Zaria, Nigeria.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.Hospital Universitário Prof. Edgard Santos. Salvador, BA, Brasil.Fundação de Hematologia e Hemoterapia da Bahia. Salvador, BA, Brasil.Fundação de Hematologia e Hemoterapia da Bahia. Salvador, BA, Brasil.Fundação de Hematologia e Hemoterapia da Bahia. Salvador, BA, Brasil.Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Farmácia. Laboratório de Pesquisa em Anemia. Departamento de Análises Clínicas. Salvador, BA, Brasil.This study investigated the effects of hydroxyurea (HU) on hematological, biochemical and inflammatory parameters in children with sickle cell anemia (SCA) in association with βS haplotype and α-thalassemia. We included 22 children with SCA who were followed for an average of 14.5 months. Laboratory parameters were assessed by electronic methods, and molecular analysis was investigated by PCR-RFLP and allele-specific PCR. Results showed significant increases in hemoglobin, HbF, hematocrit, MCV, MCH, glucose, HDL-C and albumin levels, as well as significant decreases in MCHC and AST levels, WBC, neutrophils, eosinophils, lymphocytes and reticulocytes, in children during HU therapy. HbF levels were positively correlated with hemoglobin, hematocrit, MCV and total protein, yet negatively correlated with MCHC, RDW, AAT and AST during HU therapy (p<0.05). Children who carried the Central African Republic haplotype, in response to HU therapy, presented significant increases in hemoglobin, hematocrit, triglycerides and uric acid levels, as well as significant decreases in MCHC, AST and direct bilirubin levels, WBC, neutrophils, eosinophils, lymphocytes and reticulocytes. Those with the Benin haplotype presented increases in HbF and albumin levels, and a reduction in platelet counts (p<0.05). Children with α-thalassemia presented decreased ALT during HU use, while those without this deletion presented increases in hemoglobin, hematocrit, MCV, MCH, HDL-C and albumin, as well as decreases in MCHC, neutrophils, lymphocytes, reticulocytes and AST (p<0.05). Hence, regardless of its use in association with βS haplotypes or α-thalassemia, HU seems to be linked to alterations in hemolytic, inflammatory, hepatic, lipid and glycemic profiles.engPublic Library of ScienceHidroxiureiaBiomarcadoresTalasemia alfaAnemia FalciformeCriançasHydroxyureaBiomarkersAlpha-ThalassemiaAnemia Sickle CellChildrenHydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemiainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; charset=utf-82991https://www.arca.fiocruz.br/bitstream/icict/34775/1/license.txt5a560609d32a3863062d77ff32785d58MD51ORIGINALYahouedehou, M.C.S Hydroxyurea alters.pdfYahouedehou, M.C.S Hydroxyurea 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dc.title.pt_BR.fl_str_mv Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
title Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
spellingShingle Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
Yahouédéhou, Sètondji Cocou Modeste Alexandre
Hidroxiureia
Biomarcadores
Talasemia alfa
Anemia Falciforme
Crianças
Hydroxyurea
Biomarkers
Alpha-Thalassemia
Anemia Sickle Cell
Children
title_short Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
title_full Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
title_fullStr Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
title_full_unstemmed Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
title_sort Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
author Yahouédéhou, Sètondji Cocou Modeste Alexandre
author_facet Yahouédéhou, Sètondji Cocou Modeste Alexandre
Guarda, Caroline Conceição da
Figueiredo, Camylla Vilas Boas
Santiago, Rayra Pereira
Carvalho, Suellen Pinheiro
Fiuza, Luciana Magalhães
Ndidi, Uche Samuel
Oliveira, Rodrigo Mota
Carvalho, Magda Oliveira Seixas
Nascimento, Valma Maria Lopes
Rocha, Larissa Carneiro
Lyra, Isa Menezes
Adorno, Elisângela Vitória
Goncalves, Marilda Souza
author_role author
author2 Guarda, Caroline Conceição da
Figueiredo, Camylla Vilas Boas
Santiago, Rayra Pereira
Carvalho, Suellen Pinheiro
Fiuza, Luciana Magalhães
Ndidi, Uche Samuel
Oliveira, Rodrigo Mota
Carvalho, Magda Oliveira Seixas
Nascimento, Valma Maria Lopes
Rocha, Larissa Carneiro
Lyra, Isa Menezes
Adorno, Elisângela Vitória
Goncalves, Marilda Souza
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Yahouédéhou, Sètondji Cocou Modeste Alexandre
Guarda, Caroline Conceição da
Figueiredo, Camylla Vilas Boas
Santiago, Rayra Pereira
Carvalho, Suellen Pinheiro
Fiuza, Luciana Magalhães
Ndidi, Uche Samuel
Oliveira, Rodrigo Mota
Carvalho, Magda Oliveira Seixas
Nascimento, Valma Maria Lopes
Rocha, Larissa Carneiro
Lyra, Isa Menezes
Adorno, Elisângela Vitória
Goncalves, Marilda Souza
dc.subject.other.pt_BR.fl_str_mv Hidroxiureia
Biomarcadores
Talasemia alfa
Anemia Falciforme
Crianças
topic Hidroxiureia
Biomarcadores
Talasemia alfa
Anemia Falciforme
Crianças
Hydroxyurea
Biomarkers
Alpha-Thalassemia
Anemia Sickle Cell
Children
dc.subject.en.pt_BR.fl_str_mv Hydroxyurea
Biomarkers
Alpha-Thalassemia
Anemia Sickle Cell
Children
description 1- Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (470959/2014-2 and 405595/2016-6 to MSG). http://www.cnpq.br/and 2- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001 to SCMAY, RPS, and SPC.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-08-13T16:32:26Z
dc.date.available.fl_str_mv 2019-08-13T16:32:26Z
dc.date.issued.fl_str_mv 2019
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.citation.fl_str_mv YAHOUÉDÉHOU, Sètondji Cocou Modeste Alexandre et al. Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia. Plos One, v. 14, n. 7, p. 1-13, 2019.
dc.identifier.uri.fl_str_mv https://www.arca.fiocruz.br/handle/icict/34775
dc.identifier.issn.pt_BR.fl_str_mv 1932-6203
dc.identifier.doi.none.fl_str_mv 10.1371/journal.pone.0218040
identifier_str_mv YAHOUÉDÉHOU, Sètondji Cocou Modeste Alexandre et al. Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia. Plos One, v. 14, n. 7, p. 1-13, 2019.
1932-6203
10.1371/journal.pone.0218040
url https://www.arca.fiocruz.br/handle/icict/34775
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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publisher.none.fl_str_mv Public Library of Science
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