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Ann Hepatol ; 19(1): 92-98, 2020.
Article in English | MEDLINE | ID: mdl-31607646

ABSTRACT

INTRODUCTION AND OBJECTIVES: Human immunodeficiency virus (HIV) and hepatitis C virus (HCV) co-infection generates sustained inflammation with increased reactive oxygen species production. The pathogenic impact of systemic oxidative stress is known to influence drug treatment and follow-up. The aim of this case-control study was to compare the redox status in HCV-HIV co-infected with respect to HIV-infected individuals and to explore the relation between redox and HIV follow-up variables. PATIENTS OR MATERIALS AND METHODS: Blood samples were drawn from 330 individuals divided into three groups: HIV, HCV-HIV and presumable healthy subjects. Redox, hematological, hemochemical, immunologic and virological indexes were determined. RESULTS: Both HIV groups had significant differences in global indexes of damage and antioxidant status (p<0.05) with respect to the supposedly healthy individual group. HCV-HIV group showed a significantly higher damage (total hydroperoxide and advanced oxidation protein products) compared to the control and HIV groups (p<0.05). The overall modification of the redox indexes showed that 72% of individuals with simultaneous detrimental differences were related to HCV-HIV condition. CONCLUSIONS: These results corroborate that oxidative stress occurs in the HIV condition and also during HCV-HIV co-infection, with different molecular changes of follow-up indexes. Redox indexes diagnosis should be considered in early diagnosis and treatment of HCV-HIV co-infection.


Subject(s)
HIV Infections/metabolism , Hepatitis C, Chronic/metabolism , Oxidative Stress , Adult , Advanced Oxidation Protein Products/metabolism , Anti-Retroviral Agents/therapeutic use , Antioxidants/metabolism , Antiviral Agents/therapeutic use , Case-Control Studies , Catalase/metabolism , Coinfection , Female , Glutathione/metabolism , HIV Infections/complications , HIV Infections/drug therapy , Hepatitis C, Chronic/complications , Hepatitis C, Chronic/drug therapy , Humans , Hydrogen Peroxide/metabolism , Lipid Peroxidation , Male , Malondialdehyde/metabolism , Middle Aged , Oxidants/metabolism , Superoxide Dismutase/metabolism , Viral Load
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