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

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)...

Full description

Bibliographic Details
Main Authors: Annemarie Grindel, Bianca Guggenberger, Lukas Eichberger, Christina Pöppelmeyer, Michaela Gschaider, Anela Tosevska, George Mare, David Briskey, Helmut Brath, Karl-Heinz Wagner
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5012603?pdf=render
id doaj-1099534366f9470385acc070943c385d
record_format Article
spelling doaj-1099534366f9470385acc070943c385d2020-11-24T21:40:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01119e016208210.1371/journal.pone.0162082Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2.Annemarie GrindelBianca GuggenbergerLukas EichbergerChristina PöppelmeyerMichaela GschaiderAnela TosevskaGeorge MareDavid BriskeyHelmut BrathKarl-Heinz WagnerBACKGROUND: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.http://europepmc.org/articles/PMC5012603?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Annemarie Grindel
Bianca Guggenberger
Lukas Eichberger
Christina Pöppelmeyer
Michaela Gschaider
Anela Tosevska
George Mare
David Briskey
Helmut Brath
Karl-Heinz Wagner
spellingShingle Annemarie Grindel
Bianca Guggenberger
Lukas Eichberger
Christina Pöppelmeyer
Michaela Gschaider
Anela Tosevska
George Mare
David Briskey
Helmut Brath
Karl-Heinz Wagner
Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2.
PLoS ONE
author_facet Annemarie Grindel
Bianca Guggenberger
Lukas Eichberger
Christina Pöppelmeyer
Michaela Gschaider
Anela Tosevska
George Mare
David Briskey
Helmut Brath
Karl-Heinz Wagner
author_sort Annemarie Grindel
title Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2.
title_short Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2.
title_full Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2.
title_fullStr Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2.
title_full_unstemmed Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2.
title_sort oxidative stress, dna damage and dna repair in female patients with diabetes mellitus type 2.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description 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.
url http://europepmc.org/articles/PMC5012603?pdf=render
work_keys_str_mv AT annemariegrindel oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT biancaguggenberger oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT lukaseichberger oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT christinapoppelmeyer oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT michaelagschaider oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT anelatosevska oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT georgemare oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT davidbriskey oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT helmutbrath oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
AT karlheinzwagner oxidativestressdnadamageanddnarepairinfemalepatientswithdiabetesmellitustype2
_version_ 1725924797035053056