Cargando…

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

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 haemoglo...

Descripción completa

Detalles Bibliográficos
Autores principales: Grindel, Annemarie, Brath, Helmut, Nersesyan, Armen, Knasmueller, Siegfried, Wagner, Karl-Heinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288806/
https://www.ncbi.nlm.nih.gov/pubmed/28150817
http://dx.doi.org/10.1038/srep41985
_version_ 1782504399350792192
author Grindel, Annemarie
Brath, Helmut
Nersesyan, Armen
Knasmueller, Siegfried
Wagner, Karl-Heinz
author_facet Grindel, Annemarie
Brath, Helmut
Nersesyan, Armen
Knasmueller, Siegfried
Wagner, Karl-Heinz
author_sort Grindel, Annemarie
collection PubMed
description 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.
format Online
Article
Text
id pubmed-5288806
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-52888062017-02-06 Association of Genomic Instability with HbA1c levels and Medication in Diabetic Patients Grindel, Annemarie Brath, Helmut Nersesyan, Armen Knasmueller, Siegfried Wagner, Karl-Heinz Sci Rep Article 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. Nature Publishing Group 2017-02-02 /pmc/articles/PMC5288806/ /pubmed/28150817 http://dx.doi.org/10.1038/srep41985 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Grindel, Annemarie
Brath, Helmut
Nersesyan, Armen
Knasmueller, Siegfried
Wagner, Karl-Heinz
Association of Genomic Instability with HbA1c levels and Medication in Diabetic Patients
title Association of Genomic Instability with HbA1c levels and Medication in Diabetic Patients
title_full Association of Genomic Instability with HbA1c levels and Medication in Diabetic Patients
title_fullStr Association of Genomic Instability with HbA1c levels and Medication in Diabetic Patients
title_full_unstemmed Association of Genomic Instability with HbA1c levels and Medication in Diabetic Patients
title_short Association of Genomic Instability with HbA1c levels and Medication in Diabetic Patients
title_sort association of genomic instability with hba1c levels and medication in diabetic patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288806/
https://www.ncbi.nlm.nih.gov/pubmed/28150817
http://dx.doi.org/10.1038/srep41985
work_keys_str_mv AT grindelannemarie associationofgenomicinstabilitywithhba1clevelsandmedicationindiabeticpatients
AT brathhelmut associationofgenomicinstabilitywithhba1clevelsandmedicationindiabeticpatients
AT nersesyanarmen associationofgenomicinstabilitywithhba1clevelsandmedicationindiabeticpatients
AT knasmuellersiegfried associationofgenomicinstabilitywithhba1clevelsandmedicationindiabeticpatients
AT wagnerkarlheinz associationofgenomicinstabilitywithhba1clevelsandmedicationindiabeticpatients