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Clin Chem Lab Med ; 43(4): 376-82, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15899652

RESUMO

The aim of our study was to evaluate the benefits of supplementation with 800 mg/day of alpha-tocopherol with regard to cellular viability in HIV-1 seropositive patients undergoing anti-retroviral therapy. A total of 29 patients participated in the study, of whom 14 were given the supplement and 15 a placebo. The analyses were carried out before treatment commenced and after 60, 120 and 180 days. The plasma levels of HIV-1 RNA showed a significant decrease as a consequence of treatment time in the groups studied (p = 0.0001), although the difference between the treatments over time was not verified (p = 0.7343). The percentage of viable lymphocytes showed a significant increase as a consequence of treatment time in both groups studied (p = 0.0002) and a significant difference between the treatments over time (p = 0.0472). The percentage of lymphocytes in apoptosis showed a significant reduction over time (p = 0.0003), as well as a significant difference between the treatments over time (p = 0.0321). The significant increase in cellular viability indicates that supplementation with alpha-tocopherol offers an additional positive effect on cellular preservation in HIV-1 individuals undergoing anti-retroviral therapy; however, it represents an additional risk of anti-retroviral therapeutic failure, possibly due to drug-drug interaction involving up-regulation of metabolic clearance.


Assuntos
Fármacos Anti-HIV/uso terapêutico , Antioxidantes/uso terapêutico , Infecções por HIV/tratamento farmacológico , HIV-1/efeitos dos fármacos , Linfócitos/efeitos dos fármacos , alfa-Tocoferol/uso terapêutico , Adulto , Fármacos Anti-HIV/sangue , Relação CD4-CD8 , Sobrevivência Celular/efeitos dos fármacos , Suplementos Nutricionais , Método Duplo-Cego , Quimioterapia Combinada , Feminino , HIV-1/genética , Humanos , Masculino , RNA Viral/sangue , alfa-Tocoferol/sangue
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