Literature DB >> 23085440

Impact of β(S)-globin haplotypes on oxidative stress in patients with sickle cell anemia in steady state.

Bruna Stefânia Carvalho-dos Santos1, Darcielle Bruna Dias-Elias, Lilianne Brito da Silva-Rocha, Maritza Cavalcante-Barbosa, Romélia Pinheiro-Gonçalves.   

Abstract

BACKGROUND AND AIMS: In Brazil, sickle cell anemia (SCA) is one of the most common genetic disorders. The levels of fetal hemoglobin (HbF) may be influenced by the presence of genetic modifiers; among these are the β(S)-globin haplotypes, associated with the clinical heterogeneity presented by the disease. Patients with SCA have an imbalance between the production of reactive oxygen species and antioxidant capacity, generating oxidative stress. Nitric oxide (NO) is a potent vasodilator and may be involved in the mechanism of HbF induction. The aim of this study was to evaluate the impact of β(S)-globin haplotypes in oxidative stress in patients with SCA.
METHODS: The study included 47 patients with SCA in steady state. The molecular diagnosis of SCA and characterization of the β(S)-globin haplotype was performed by β(S) chain polymerase chain reaction-restriction fragment length polymorphisms (PCR-RFLP). Concentration of HbF was determined by high-performance liquid chromatography (HPLC). Serum levels of nitrite/nitrate (NOx) and malondialdehyde were determined by spectrophotometry.
RESULTS: The most prevalent haplotype in the study population was Bantu. The Benin/n group presented significantly higher HbF and nitrite levels as compared to the Bantu/n group.
CONCLUSIONS: Our results confirm data reported in the literature where the Benin and Bantu haplotypes are respectively correlated to high levels and decreased HbF. In addition, haplotypes associated with high levels of HbF showed high levels of nitrite, demonstrating that as the HbF, serum levels of NOx may prove useful as a prognostic biomarker in patients with SCA.
Copyright © 2012 IMSS. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23085440     DOI: 10.1016/j.arcmed.2012.08.014

Source DB:  PubMed          Journal:  Arch Med Res        ISSN: 0188-4409            Impact factor:   2.235


  3 in total

1.  Clinical phenotypes and the biological parameters of Congolese patients suffering from sickle cell anemia: A first report from Central Africa.

Authors:  Tite M Mikobi; Prosper Lukusa Tshilobo; Michel N Aloni; Pierre Z Akilimali; Georges Mvumbi-Lelo; Jean Marie Mbuyi-Muamba
Journal:  J Clin Lab Anal       Date:  2017-01-23       Impact factor: 2.352

2.  Sickle cell anemia: clinical diversity and beta S-globin haplotypes.

Authors:  Sandra Regina Loggetto
Journal:  Rev Bras Hematol Hemoter       Date:  2013

3.  High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte.

Authors:  Abdourahim Chamouine; Thoueiba Saandi; Mathias Muszlak; Juliette Larmaraud; Laurent Lambrecht; Jean Poisson; Julien Balicchi; Serge Pissard; Narcisse Elenga
Journal:  BMC Pediatr       Date:  2020-06-20       Impact factor: 2.125

  3 in total

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