Oxidative stress in hepatitis C virus-human immunodeficiency virus co-infected patients

Ann Hepatol. 2020 Jan-Feb;19(1):92-98. doi: 10.1016/j.aohep.2019.05.009. Epub 2019 Sep 12.

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.

Keywords: Aids; HCV; HIV; Redox alterations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 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
  • HIV Infections / metabolism*
  • Hepatitis C, Chronic / complications
  • Hepatitis C, Chronic / drug therapy
  • Hepatitis C, Chronic / metabolism*
  • Humans
  • Hydrogen Peroxide / metabolism
  • Lipid Peroxidation
  • Male
  • Malondialdehyde / metabolism
  • Middle Aged
  • Oxidants / metabolism
  • Oxidative Stress*
  • Superoxide Dismutase / metabolism
  • Viral Load

Substances

  • Advanced Oxidation Protein Products
  • Anti-Retroviral Agents
  • Antioxidants
  • Antiviral Agents
  • Oxidants
  • Malondialdehyde
  • Hydrogen Peroxide
  • Catalase
  • Superoxide Dismutase
  • Glutathione