TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia

Detalhes bibliográficos
Autor(a) principal: Lyra, Isa Menezes
Data de Publicação: 2011
Outros Autores: Moura Neto, José Pereira de, Reis, Mitermayer Galvão dos, Barbosa, Cynara Gomes, Gonçalves, Marilda de Souza, Cerqueira, Bruno Antonio Veloso, Couto, Fábio David, Cajado, C., Santos, Wendell Vilas Boas, Dorea, M. J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFBA
Texto Completo: http://www.repositorio.ufba.br/ri/handle/ri/5422
Resumo: texto completo: acesso restrito. p. 312–317.
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spelling Lyra, Isa MenezesMoura Neto, José Pereira deReis, Mitermayer Galvão dosBarbosa, Cynara GomesGonçalves, Marilda de SouzaCerqueira, Bruno Antonio VelosoCouto, Fábio DavidCajado, C.Santos, Wendell Vilas BoasDorea, M. J.Lyra, Isa MenezesMoura Neto, José Pereira deReis, Mitermayer Galvão dosBarbosa, Cynara GomesGonçalves, Marilda de SouzaCerqueira, Bruno Antonio VelosoCouto, Fábio DavidCajado, C.Santos, Wendell Vilas BoasDorea, M. J.2012-02-23T17:08:28Z20111096-0023http://www.repositorio.ufba.br/ri/handle/ri/5422v. 56.texto completo: acesso restrito. p. 312–317.Sickle cell anemia (SCA) is a disorder characterized by a heterogeneous clinical outcome. In the present study, we investigated the associations between Tumor Necrosis Factor-alpha (TNF-alpha) ÿ308G>A and Interleukin 8 (IL-8) ÿ251A>T gene polymorphisms, medical history and classical biomarkers in children with steady-state SCA. In total, 210 SCA patients aged 2–21 years and 200 healthy controls were studied. Gene polymorphisms, betaS-globin haplotypes and a 3.7-kb deletion in alpha2-thalassemia (a2-thal3.7 kb) were investigated by PCR/RFLP analysis, and cytokine levels were determined by ELISA. Splenomegaly (p = .032) was more prevalent among children younger than 5 years of age. The A allele of the TNF-alpha ÿ308G>A gene polymorphism and the presence of a2-thal3.7 kb were associated with an increase risk of splenic sequestration events (p = .001; p = .046), while the T allele of the IL-8 ÿ251A>T gene polymor-phism was considered to be a protective factor for splenomegaly events (p = .032). Moreover, the A allele of the TNF-alpha ÿ308G>A gene polymorphism was associated with high TNF-alpha levels (p = .021), and the hemoglobin F and hemoglobin S haplotypes were correlated with serum levels of IL-8. The logistic regression analysis showed significant effects of the TNF-alpha and IL-8 gene polymorphisms, betaS-globin gene haplotypes and a2-thal3.7 kb on the occurrence of splenic sequestration events. Our study empha-sizes that the identification of new genetic and immunological biomarkers and their associations with classical markers is an important strategy to elucidate the underlying causes of different SCA phenotypes and their effects on patient outcome.Submitted by Ana Valéria de Jesus Moura (anavaleria_131@hotmail.com) on 2012-02-23T17:08:28Z No. of bitstreams: 1 __pdn.sciencedirect.com_....0-S1043466611002201-main.pdf: 165270 bytes, checksum: 0e51b46fddf119fd4edc9fc0857708a9 (MD5)Made available in DSpace on 2012-02-23T17:08:28Z (GMT). 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dc.title.pt_BR.fl_str_mv TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
dc.title.alternative.pt_BR.fl_str_mv Cytokine
title TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
spellingShingle TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
Lyra, Isa Menezes
TNF-alpha
IL-8
Sickle cell anemia
betaS-globin Gene haplotypes
alpha2-Thalassemia
title_short TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
title_full TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
title_fullStr TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
title_full_unstemmed TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
title_sort TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
author Lyra, Isa Menezes
author_facet Lyra, Isa Menezes
Moura Neto, José Pereira de
Reis, Mitermayer Galvão dos
Barbosa, Cynara Gomes
Gonçalves, Marilda de Souza
Cerqueira, Bruno Antonio Veloso
Couto, Fábio David
Cajado, C.
Santos, Wendell Vilas Boas
Dorea, M. J.
author_role author
author2 Moura Neto, José Pereira de
Reis, Mitermayer Galvão dos
Barbosa, Cynara Gomes
Gonçalves, Marilda de Souza
Cerqueira, Bruno Antonio Veloso
Couto, Fábio David
Cajado, C.
Santos, Wendell Vilas Boas
Dorea, M. J.
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Lyra, Isa Menezes
Moura Neto, José Pereira de
Reis, Mitermayer Galvão dos
Barbosa, Cynara Gomes
Gonçalves, Marilda de Souza
Cerqueira, Bruno Antonio Veloso
Couto, Fábio David
Cajado, C.
Santos, Wendell Vilas Boas
Dorea, M. J.
Lyra, Isa Menezes
Moura Neto, José Pereira de
Reis, Mitermayer Galvão dos
Barbosa, Cynara Gomes
Gonçalves, Marilda de Souza
Cerqueira, Bruno Antonio Veloso
Couto, Fábio David
Cajado, C.
Santos, Wendell Vilas Boas
Dorea, M. J.
dc.subject.por.fl_str_mv TNF-alpha
IL-8
Sickle cell anemia
betaS-globin Gene haplotypes
alpha2-Thalassemia
topic TNF-alpha
IL-8
Sickle cell anemia
betaS-globin Gene haplotypes
alpha2-Thalassemia
description texto completo: acesso restrito. p. 312–317.
publishDate 2011
dc.date.issued.fl_str_mv 2011
dc.date.accessioned.fl_str_mv 2012-02-23T17:08:28Z
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dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://www.repositorio.ufba.br/ri/handle/ri/5422
dc.identifier.issn.none.fl_str_mv 1096-0023
dc.identifier.number.pt_BR.fl_str_mv v. 56.
identifier_str_mv 1096-0023
v. 56.
url http://www.repositorio.ufba.br/ri/handle/ri/5422
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.source.pt_BR.fl_str_mv doi:10.1016/j.cyto.2011.07.002
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