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J Pediatr ; 195: 228-235, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29449005

RESUMO

OBJECTIVES: To investigate the associations between several sickle cell disease genetic modifiers (beta-globin haplotypes, alpha-thalassemia, and glucose-6-phosphate dehydrogenase deficiency) and the level of oxidative stress and to evaluate the association between oxidative stress and the rates of vaso-occlusive events. STUDY DESIGN: Steady-state oxidative and nitrosative stress markers, biological variables, genetic modulators, and vaso-occlusive crisis events requiring emergency admissions were measured during a 2-year period in 62 children with sickle cell anemia (58 SS and 4 Sß0). Twelve ethnic-matched children without sickle cell anemia also participated as healthy controls (AA) for oxidative and nitrosative stress level measurement. RESULTS: Oxidative and nitrosative stress were greater in patients with sickle cell anemia compared with control patients, but the rate of vaso-occlusive crisis events in sickle cell anemia was not associated with the level of oxidative stress. The presence of alpha-thalassemia, but not glucose-6-phosphate dehydrogenase deficiency or beta-globin haplotype, modulated the level of oxidative stress in children with sickle cell anemia. CONCLUSION: Mild hemolysis in children with alpha-thalassemia may limit oxidative stress and could explain the protective role of alpha-thalassemia in hemolysis-related sickle cell complications.


Assuntos
Anemia Falciforme/genética , Anemia Falciforme/fisiopatologia , Predisposição Genética para Doença , Estresse Oxidativo , Índice de Gravidade de Doença , Adolescente , Anemia Falciforme/diagnóstico , Criança , Pré-Escolar , Feminino , Seguimentos , Marcadores Genéticos , Humanos , Modelos Lineares , Masculino , Estudos Retrospectivos , Fatores de Risco
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