Redox imbalance in peripheral blood of type 1 myotonic dystrophy patients

Redox Rep. 2016 Sep;21(5):232-7. doi: 10.1080/13510002.2015.1107311. Epub 2016 Feb 5.

Abstract

Objectives: The aim of our study was to determine if redox imbalance caused by the activities of antioxidant enzymes existed in erythrocytes of type 1 myotonic dystrophy (DM1) patients.

Methods: The activities of erythrocyte superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase were measured in 30 DM1 patients and 15 healthy controls (HCs). The obtained values were correlated with the Muscular Impairment Rating Scale (MIRS) score and creatine kinase (CK).

Results: Superoxide dismutase and catalase activities were lower in DM1 patients compared to HCs. A positive correlation was found between disease duration and MIRS score as well as with glutathione reductase activity. In DM1 patients, there were positive correlations between catalase, glutathione peroxidase, and glutathione reductase activities. After sub-dividing DM1 patients according to CK levels, superoxide dismutase activity was still statistically different from HCs. However, catalase activity was significantly lower only in DM1 patients with increased CK.

Discussion: Undesirable alterations in antioxidant enzyme activities during DM1 disease progression may result in conditions favoring oxidative stress and changes in metabolism which together could contribute to muscle wasting.

Keywords: Catalase; Erythrocytes; Glutathione reductase; Glutatione peroxidase; Superoxide dismutase; Type 1 myotonic dystrophy.

MeSH terms

  • Adult
  • Catalase / metabolism
  • Erythrocytes / metabolism
  • Female
  • Glutathione Peroxidase / metabolism
  • Glutathione Reductase / metabolism
  • Humans
  • Male
  • Myotonic Dystrophy / metabolism*
  • Myotonic Dystrophy / pathology
  • Oxidation-Reduction
  • Oxidative Stress / physiology
  • Superoxide Dismutase / metabolism

Substances

  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Glutathione Reductase