Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2

PLoS One. 2016 Sep 6;11(9):e0162082. doi: 10.1371/journal.pone.0162082. eCollection 2016.

Abstract

Background: Diabetes mellitus type 2 (T2DM) is associated with oxidative stress which in turn can lead to DNA damage. The aim of the present study was to analyze oxidative stress, DNA damage and DNA repair in regard to hyperglycemic state and diabetes duration.

Methods: Female T2DM patients (n = 146) were enrolled in the MIKRODIAB study and allocated in two groups regarding their glycated hemoglobin (HbA1c) level (HbA1c≤7.5%, n = 74; HbA1c>7.5%, n = 72). In addition, tertiles according to diabetes duration (DD) were created (DDI = 6.94±3.1 y, n = 49; DDII = 13.35±1.1 y, n = 48; DDIII = 22.90±7.3 y, n = 49). Oxidative stress parameters, including ferric reducing ability potential, malondialdehyde, oxidized and reduced glutathione, reduced thiols, oxidized LDL and F2-Isoprostane as well as the activity of antioxidant enzymes superoxide dismutase, catalase and glutathione peroxidase were measured. Damage to DNA was analyzed in peripheral blood mononuclear cells and whole blood with single cell gel electrophoresis. DNA base excision repair capacity was tested with the modified comet repair assay. Additionally, mRNA expressions of nine genes related to base excision repair were analyzed in a subset of 46 matched individuals.

Results: No significant differences in oxidative stress parameters, antioxidant enzyme activities, damage to DNA and base excision repair capacity, neither between a HbA1c cut off />7.5%, nor between diabetes duration was found. A significant up-regulation in mRNA expression was found for APEX1, LIG3 and XRCC1 in patients with >7.5% HbA1c. Additionally, we observed higher total cholesterol, LDL-cholesterol, LDL/HDL-cholesterol, triglycerides, Framingham risk score, systolic blood pressure, BMI and lower HDL-cholesterol in the hyperglycemic group.

Conclusion: BMI, blood pressure and blood lipid status were worse in hyperglycemic individuals. However, no major disparities regarding oxidative stress, damage to DNA and DNA repair were present which might be due to good medical treatment with regular health checks in T2DM patients in Austria.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Blood Pressure
  • Body Mass Index
  • Catalase / blood
  • Catalase / genetics
  • Cholesterol, HDL / blood
  • Cholesterol, LDL / blood
  • Cross-Sectional Studies
  • DNA Damage*
  • DNA Ligase ATP
  • DNA Ligases / blood
  • DNA Ligases / genetics
  • DNA Repair*
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / blood
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / genetics
  • DNA-Binding Proteins / blood
  • DNA-Binding Proteins / genetics
  • Diabetes Mellitus, Type 2 / diagnosis*
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / pathology
  • F2-Isoprostanes / blood
  • Female
  • Gene Expression Regulation
  • Glutathione / blood
  • Glutathione Peroxidase / blood
  • Glutathione Peroxidase / genetics
  • Glycated Hemoglobin / metabolism
  • Humans
  • Hypoglycemic Agents / therapeutic use
  • Leukocytes, Mononuclear / chemistry
  • Lipoproteins, LDL / blood
  • Malondialdehyde / blood
  • Middle Aged
  • Oxidative Stress*
  • Poly-ADP-Ribose Binding Proteins
  • Superoxide Dismutase / blood
  • Superoxide Dismutase / genetics
  • Triglycerides / blood
  • X-ray Repair Cross Complementing Protein 1
  • Xenopus Proteins

Substances

  • Cholesterol, HDL
  • Cholesterol, LDL
  • DNA-Binding Proteins
  • F2-Isoprostanes
  • Glycated Hemoglobin A
  • Hypoglycemic Agents
  • Lipoproteins, LDL
  • Poly-ADP-Ribose Binding Proteins
  • Triglycerides
  • X-ray Repair Cross Complementing Protein 1
  • XRCC1 protein, human
  • Xenopus Proteins
  • hemoglobin A1c protein, human
  • oxidized low density lipoprotein
  • Malondialdehyde
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • APEX1 protein, human
  • DNA-(Apurinic or Apyrimidinic Site) Lyase
  • DNA Ligases
  • DNA Ligase ATP
  • DNA ligase III alpha protein, Xenopus
  • LIG3 protein, human
  • Glutathione

Grants and funding

This article was supported by the Open Access Publishing Fund of the University of Vienna. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.