Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease

Detalhes bibliográficos
Autor(a) principal: Izabel Cristina Justino Bandeira
Data de Publicação: 2013
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UFC
Texto Completo: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17300
Resumo: The Sickle Cell Anemia (SCA) is an inherited disease characterized by homozygous severe hemolytic anemia and clinical variables, considered a chronic inflammatory disease. SCA results from a mutation in a nitrogenous base in the sixth codon of the beta globin gene, leading to substitution of adenine for thymine nucleotide (GAG → GTG), which results in the production of the amino acid valine in place of glutamic acid. The inflammatory pathophysiology of SCA is centered on the ability of HbS polymerization that leads to chronic hemolysis and vaso-occlusion. SCA patients are a chronic inflammatory state of multifactorial origin that involves endothelial cells, erythrocytes, leukocytes and platelets by increasing the interactions between cell-cell and cell-endothelium starting an endothelial injury. The study was a cross-sectional prospective in order to investigate the association of haplotypes with the inflammatory profile of patients with AF. Was performed to confirm the HbSS and then study the haplotypes BS mutation in the gene for beta globin chain. We measured markers IL-6, IL-8, TNF-α, IL-17, CRP, IL-10 and TGF-β on 67 patients with SCA and 26 healthy subjects. We observed the prevalence of Bantu haplotype (67.1%) in the patient population studied, followed by the Benin haplotype (28.3%). The study confirms that SCA patients are in a chronic inflammatory state, as had elevated markers of proinflammatory and anti-inflammatory when compared to healthy subjects. The Bantu achieved higher levels of proinflammatory cytokines and CRP compared to the values for Haplotype Benin. For the anti-inflammatory profile, Bantu haplotype also showed high levels of the markers when compared to patients Benin haplotype. Then, the inflammatory profile of patients with SCA is associated with genetic polymorphisms.
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spelling info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisStudy of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell diseaseEstudo dos marcadores de inflamaÃÃo: associaÃÃo com os haplÃtipos do cluster da β-globina na anemia falciforme 2013-02-20RomÃlia Pinheiro GonÃalves Lemes28620062387http://lattes.cnpq.br/8202510508068072ArlÃndia Cristina Lima Nobre de Morais40410706353http://lattes.cnpq.br/2247671773636111Herivaldo Ferreira da Silva14280566372http://lattes.cnpq.br/6218902396923156Maria da Silva Pitombeira00117412368http://buscatextual.cnpq.br/buscatextual/visualizacv.jsp?id=K4787973H900341813346http://lattes.cnpq.br/5090909997386976Izabel Cristina Justino BandeiraUniversidade Federal do CearÃPrograma de PÃs-GraduaÃÃo em PatologiaUFCBRANATOMIA PATOLOGICA E PATOLOGIA CLINICAThe Sickle Cell Anemia (SCA) is an inherited disease characterized by homozygous severe hemolytic anemia and clinical variables, considered a chronic inflammatory disease. SCA results from a mutation in a nitrogenous base in the sixth codon of the beta globin gene, leading to substitution of adenine for thymine nucleotide (GAG → GTG), which results in the production of the amino acid valine in place of glutamic acid. The inflammatory pathophysiology of SCA is centered on the ability of HbS polymerization that leads to chronic hemolysis and vaso-occlusion. SCA patients are a chronic inflammatory state of multifactorial origin that involves endothelial cells, erythrocytes, leukocytes and platelets by increasing the interactions between cell-cell and cell-endothelium starting an endothelial injury. The study was a cross-sectional prospective in order to investigate the association of haplotypes with the inflammatory profile of patients with AF. Was performed to confirm the HbSS and then study the haplotypes BS mutation in the gene for beta globin chain. We measured markers IL-6, IL-8, TNF-α, IL-17, CRP, IL-10 and TGF-β on 67 patients with SCA and 26 healthy subjects. We observed the prevalence of Bantu haplotype (67.1%) in the patient population studied, followed by the Benin haplotype (28.3%). The study confirms that SCA patients are in a chronic inflammatory state, as had elevated markers of proinflammatory and anti-inflammatory when compared to healthy subjects. The Bantu achieved higher levels of proinflammatory cytokines and CRP compared to the values for Haplotype Benin. For the anti-inflammatory profile, Bantu haplotype also showed high levels of the markers when compared to patients Benin haplotype. Then, the inflammatory profile of patients with SCA is associated with genetic polymorphisms. A Anemia Falciforme (AF) à uma doenÃa hereditÃria homozigÃtica caracterizada por anemia hemolÃtica grave e manifestaÃÃes clÃnicas variÃveis, considerada uma doenÃa inflamatÃria crÃnica. A AF resulta de uma mutaÃÃo pontual em uma base nitrogenada no sexto cÃdon do gene da beta globina, levando a substituiÃÃo do nucleotÃdeo adenina por timina (GAG → GTG), o que resulta na produÃÃo do aminoÃcido valina no lugar do Ãcido glutÃmico. A fisiopatologia inflamatÃria da AF està centralizada na capacidade de polimerizaÃÃo da HbS que leva à hemÃlise crÃnica e à vaso-oclusÃo. Os pacientes com AF encontram-se em um estado inflamatÃrio crÃnico de origem multifatorial, que envolve cÃlulas endoteliais, eritrÃcitos, leucÃcitos e plaquetas atravÃs do aumento nas interaÃÃes entre cÃlula-cÃlula e cÃlula-endotÃlio iniciando uma lesÃo endotelial. O estudo foi do tipo transversal prospectivo com a finalidade de investigar a associaÃÃo dos haplÃtipos com o perfil inflamatÃrio de pacientes com AF. Foi realizada a confirmaÃÃo da HbSS e em seguida o estudo dos haplÃtipos da mutaÃÃo BS no gene da cadeia beta globÃnica. Foram dosados os marcadores IL-6, IL-8, TNF-α, IL-17, PCR-us, IL-10 e TGF-β em 67 pacientes com AF e em 26 indivÃduos saudÃveis. Observou-se a prevalÃncia do haplÃtipo Bantu (67,1%) na populaÃÃo de pacientes estudada, seguido do haplÃtipo Benin (28,3%). O estudo confirma que os pacientes com AF encontram-se em um estado inflamatÃrio crÃnico, pois apresentaram valores elevados de marcadores prÃ-inflamatÃrios e antiinflamatÃrio, quando comparadas à indivÃduos saudÃveis. O haplÃtipo Bantu obteve mais elevados Ãndices das citocinas prÃ-inflamatÃrias e da PCR-us quando comparados aos valores para o HaplÃtipo Benin. Para o perfil antiinflamatÃrio, o haplÃtipo Bantu tambÃm apresentou valores elevados dos marcadores, quando comparados aos pacientes de haplÃtipo Benin. EntÃo, o perfil inflamatÃrio dos pacientes com AF està associado à polimorfismos genÃticos. Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgicohttp://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17300application/pdfinfo:eu-repo/semantics/openAccessporreponame:Biblioteca Digital de Teses e Dissertações da UFCinstname:Universidade Federal do Cearáinstacron:UFC2019-01-21T11:30:43Zmail@mail.com -
dc.title.en.fl_str_mv Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease
dc.title.alternative.pt.fl_str_mv Estudo dos marcadores de inflamaÃÃo: associaÃÃo com os haplÃtipos do cluster da β-globina na anemia falciforme
title Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease
spellingShingle Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease
Izabel Cristina Justino Bandeira
ANATOMIA PATOLOGICA E PATOLOGIA CLINICA
title_short Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease
title_full Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease
title_fullStr Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease
title_full_unstemmed Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease
title_sort Study of a marker of inflammation: association with cluster of haplotypes β-globin in sickle cell disease
author Izabel Cristina Justino Bandeira
author_facet Izabel Cristina Justino Bandeira
author_role author
dc.contributor.advisor1.fl_str_mv RomÃlia Pinheiro GonÃalves Lemes
dc.contributor.advisor1ID.fl_str_mv 28620062387
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/8202510508068072
dc.contributor.referee1.fl_str_mv ArlÃndia Cristina Lima Nobre de Morais
dc.contributor.referee1ID.fl_str_mv 40410706353
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/2247671773636111
dc.contributor.referee2.fl_str_mv Herivaldo Ferreira da Silva
dc.contributor.referee2ID.fl_str_mv 14280566372
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/6218902396923156
dc.contributor.referee3.fl_str_mv Maria da Silva Pitombeira
dc.contributor.referee3ID.fl_str_mv 00117412368
dc.contributor.referee3Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.jsp?id=K4787973H9
dc.contributor.authorID.fl_str_mv 00341813346
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/5090909997386976
dc.contributor.author.fl_str_mv Izabel Cristina Justino Bandeira
contributor_str_mv RomÃlia Pinheiro GonÃalves Lemes
ArlÃndia Cristina Lima Nobre de Morais
Herivaldo Ferreira da Silva
Maria da Silva Pitombeira
dc.subject.cnpq.fl_str_mv ANATOMIA PATOLOGICA E PATOLOGIA CLINICA
topic ANATOMIA PATOLOGICA E PATOLOGIA CLINICA
dc.description.sponsorship.fl_txt_mv Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico
dc.description.abstract.por.fl_txt_mv The Sickle Cell Anemia (SCA) is an inherited disease characterized by homozygous severe hemolytic anemia and clinical variables, considered a chronic inflammatory disease. SCA results from a mutation in a nitrogenous base in the sixth codon of the beta globin gene, leading to substitution of adenine for thymine nucleotide (GAG → GTG), which results in the production of the amino acid valine in place of glutamic acid. The inflammatory pathophysiology of SCA is centered on the ability of HbS polymerization that leads to chronic hemolysis and vaso-occlusion. SCA patients are a chronic inflammatory state of multifactorial origin that involves endothelial cells, erythrocytes, leukocytes and platelets by increasing the interactions between cell-cell and cell-endothelium starting an endothelial injury. The study was a cross-sectional prospective in order to investigate the association of haplotypes with the inflammatory profile of patients with AF. Was performed to confirm the HbSS and then study the haplotypes BS mutation in the gene for beta globin chain. We measured markers IL-6, IL-8, TNF-α, IL-17, CRP, IL-10 and TGF-β on 67 patients with SCA and 26 healthy subjects. We observed the prevalence of Bantu haplotype (67.1%) in the patient population studied, followed by the Benin haplotype (28.3%). The study confirms that SCA patients are in a chronic inflammatory state, as had elevated markers of proinflammatory and anti-inflammatory when compared to healthy subjects. The Bantu achieved higher levels of proinflammatory cytokines and CRP compared to the values for Haplotype Benin. For the anti-inflammatory profile, Bantu haplotype also showed high levels of the markers when compared to patients Benin haplotype. Then, the inflammatory profile of patients with SCA is associated with genetic polymorphisms.
A Anemia Falciforme (AF) à uma doenÃa hereditÃria homozigÃtica caracterizada por anemia hemolÃtica grave e manifestaÃÃes clÃnicas variÃveis, considerada uma doenÃa inflamatÃria crÃnica. A AF resulta de uma mutaÃÃo pontual em uma base nitrogenada no sexto cÃdon do gene da beta globina, levando a substituiÃÃo do nucleotÃdeo adenina por timina (GAG → GTG), o que resulta na produÃÃo do aminoÃcido valina no lugar do Ãcido glutÃmico. A fisiopatologia inflamatÃria da AF està centralizada na capacidade de polimerizaÃÃo da HbS que leva à hemÃlise crÃnica e à vaso-oclusÃo. Os pacientes com AF encontram-se em um estado inflamatÃrio crÃnico de origem multifatorial, que envolve cÃlulas endoteliais, eritrÃcitos, leucÃcitos e plaquetas atravÃs do aumento nas interaÃÃes entre cÃlula-cÃlula e cÃlula-endotÃlio iniciando uma lesÃo endotelial. O estudo foi do tipo transversal prospectivo com a finalidade de investigar a associaÃÃo dos haplÃtipos com o perfil inflamatÃrio de pacientes com AF. Foi realizada a confirmaÃÃo da HbSS e em seguida o estudo dos haplÃtipos da mutaÃÃo BS no gene da cadeia beta globÃnica. Foram dosados os marcadores IL-6, IL-8, TNF-α, IL-17, PCR-us, IL-10 e TGF-β em 67 pacientes com AF e em 26 indivÃduos saudÃveis. Observou-se a prevalÃncia do haplÃtipo Bantu (67,1%) na populaÃÃo de pacientes estudada, seguido do haplÃtipo Benin (28,3%). O estudo confirma que os pacientes com AF encontram-se em um estado inflamatÃrio crÃnico, pois apresentaram valores elevados de marcadores prÃ-inflamatÃrios e antiinflamatÃrio, quando comparadas à indivÃduos saudÃveis. O haplÃtipo Bantu obteve mais elevados Ãndices das citocinas prÃ-inflamatÃrias e da PCR-us quando comparados aos valores para o HaplÃtipo Benin. Para o perfil antiinflamatÃrio, o haplÃtipo Bantu tambÃm apresentou valores elevados dos marcadores, quando comparados aos pacientes de haplÃtipo Benin. EntÃo, o perfil inflamatÃrio dos pacientes com AF està associado à polimorfismos genÃticos.
description The Sickle Cell Anemia (SCA) is an inherited disease characterized by homozygous severe hemolytic anemia and clinical variables, considered a chronic inflammatory disease. SCA results from a mutation in a nitrogenous base in the sixth codon of the beta globin gene, leading to substitution of adenine for thymine nucleotide (GAG → GTG), which results in the production of the amino acid valine in place of glutamic acid. The inflammatory pathophysiology of SCA is centered on the ability of HbS polymerization that leads to chronic hemolysis and vaso-occlusion. SCA patients are a chronic inflammatory state of multifactorial origin that involves endothelial cells, erythrocytes, leukocytes and platelets by increasing the interactions between cell-cell and cell-endothelium starting an endothelial injury. The study was a cross-sectional prospective in order to investigate the association of haplotypes with the inflammatory profile of patients with AF. Was performed to confirm the HbSS and then study the haplotypes BS mutation in the gene for beta globin chain. We measured markers IL-6, IL-8, TNF-α, IL-17, CRP, IL-10 and TGF-β on 67 patients with SCA and 26 healthy subjects. We observed the prevalence of Bantu haplotype (67.1%) in the patient population studied, followed by the Benin haplotype (28.3%). The study confirms that SCA patients are in a chronic inflammatory state, as had elevated markers of proinflammatory and anti-inflammatory when compared to healthy subjects. The Bantu achieved higher levels of proinflammatory cytokines and CRP compared to the values for Haplotype Benin. For the anti-inflammatory profile, Bantu haplotype also showed high levels of the markers when compared to patients Benin haplotype. Then, the inflammatory profile of patients with SCA is associated with genetic polymorphisms.
publishDate 2013
dc.date.issued.fl_str_mv 2013-02-20
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.publisher.none.fl_str_mv Universidade Federal do CearÃ
dc.publisher.program.fl_str_mv Programa de PÃs-GraduaÃÃo em Patologia
dc.publisher.initials.fl_str_mv UFC
dc.publisher.country.fl_str_mv BR
publisher.none.fl_str_mv Universidade Federal do CearÃ
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da UFC
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instname_str Universidade Federal do Ceará
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