Association of Genomic Instability with HbA1c levels and Medication in Diabetic Patients

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作者
Annemarie Grindel
Helmut Brath
Armen Nersesyan
Siegfried Knasmueller
Karl-Heinz Wagner
机构
[1] Emerging Field Oxidative Stress and DNA Stability,Department of Nutritional Sciences
[2] University of Vienna,undefined
[3] Research Platform Active Ageing,undefined
[4] University of Vienna,undefined
[5] Diabetes Outpatient Clinic,undefined
[6] Health Centre South,undefined
[7] Institute for Cancer Research,undefined
[8] Medical University Vienna,undefined
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摘要
Diabetes Mellitus type 2 (DM2) is associated with increased cancer risk. Instability of the genetic material plays a key role in the aetiology of human cancer. This study aimed to analyse genomic instability with the micronucleus cytome assay in exfoliated buccal cells depending on glycated haemoglobin (HbA1c) levels and medication in 146 female DM2 patients. The occurrence of micronuclei was significantly increased in DM2 patients compared to healthy controls. Furthermore, it was doubled in DM2 patients with HbA1c > 7.5% compared to subjects with HbA1c ≤ 7.5%. Positive correlations were found between micronuclei frequencies and HbA1c as well as fasting plasma glucose. Patients under insulin treatment showed a two-fold increase in micronuclei frequencies compared to subjects under first-line medication (no drugs or monotherapy with non-insulin medication). However, after separation of HbA1c (cut-off 7.5%) only patients with severe DM2 characterised by high HbA1c and insulin treatment showed higher micronuclei frequencies but not patients with insulin treatment and low HbA1c. We demonstrated that the severity of DM2 accompanied by elevated micronuclei frequencies predict a possible enhanced cancer risk among female DM2 patients. Therapy, therefore, should focus on a strict HbA1c control and personalised medical treatments.
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