Polymorphic differences in SOD-2 may influence HCV viral clearance

J Med Virol. 2014 Jun;86(6):941-7. doi: 10.1002/jmv.23923. Epub 2014 Mar 7.

Abstract

Hepatitis C virus (HCV) is a pathogen causing chronic hepatitis, cirrhosis, and liver cancer occurring in about 3% of the world's population. Most individuals infected with HCV develop persistent viremia. Oxidative stress may play an important role in the pathogenesis of a number of diseases including HCV infection and diabetes mellitus. Polymorphisms in the antioxidant genes may determine cellular oxidative stress levels as a primary pathogenic role in HCV and/or in its complications. Patients with HCV and normal, healthy controls were investigated for a superoxide dismutase (SOD-2) polymorphism in the mitochondrial targeting sequence with Ala/Val (C-9T) substitution. Polymorphisms in antioxidant gene SOD-2 were carried out by PCR, restriction fragment length polymorphism assays and by polyacrylamide gel electrophoresis. For the SOD-2 polymorphism, the RNA positive group showed a higher percentage of "CT" genotype than the RNA negative group (89.3% vs. 66.1%, P = 0.001, χ(2) = 11.9). The RNA negative group had more TT genotypes than the RNA positive group (27.4% vs. 6.80%, P = 0.01, χ(2) = 11.6). The exposed uninfected group had an increased frequency of the "CT" genotype (86.2% vs. 66.1%, P = 0.02, χ(2) = 5.5). The RNA positives had a higher frequency of the "CT" from the normal controls (72.1% vs. 89.2%, P = 0.005, χ(2) = 7.8).

Keywords: SOD-2; antioxidant; gene polymorphism; hepatitis C; virus clearance.

MeSH terms

  • Adult
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Genetic Predisposition to Disease*
  • Hepacivirus / immunology*
  • Hepatitis C / immunology*
  • Humans
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Polymorphism, Single Nucleotide
  • Retrospective Studies
  • Superoxide Dismutase / genetics*
  • Superoxide Dismutase / metabolism*

Substances

  • Superoxide Dismutase
  • superoxide dismutase 2