Cargando…

Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1

The present study investigates the relationship between diabetes metabolic control represented by levels of HbA1c, early glycation products-(fructosamine (FAM)), serum-advanced glycation end products (s-AGEs), lipoperoxidation products (LPO), advanced oxidation protein products (AOPP) and circulatin...

Descripción completa

Detalles Bibliográficos
Autores principales: Jakuš, Vladimír, Sapák, Michal, Kostolanská, Jana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463181/
https://www.ncbi.nlm.nih.gov/pubmed/23049541
http://dx.doi.org/10.1155/2012/510902
_version_ 1782245270202875904
author Jakuš, Vladimír
Sapák, Michal
Kostolanská, Jana
author_facet Jakuš, Vladimír
Sapák, Michal
Kostolanská, Jana
author_sort Jakuš, Vladimír
collection PubMed
description The present study investigates the relationship between diabetes metabolic control represented by levels of HbA1c, early glycation products-(fructosamine (FAM)), serum-advanced glycation end products (s-AGEs), lipoperoxidation products (LPO), advanced oxidation protein products (AOPP) and circulating TGF-β in young patients with DM1. The study group consisted of 79 patients with DM1 (8–18 years). 31 healthy children were used as control (1–16 years). Baseline characteristics of patients were compared by Student's t-test and nonparametric Mann-Whitney test (Statdirect), respectively. The correlations between the measured parameters were examined using Pearson correlation coefficient r and Spearman's rank test, respectively. A P value < 0.05 was considered as statistically significant. HbA1c was measured by LPLC, s-AGEs spectrofluorimetrically, LPO and AOPP spectrophotometrically and TGF-β by ELISA. Our results showed that parameters of glycation and oxidation are significantly higher in patients with DM1 than in healthy control. The level of serum TGF-β was significantly higher in diabetics in comparison with control: 7.1(3.6; 12.6) versus 1.6(0.8; 3.9) ng/mL. TGF-β significantly correlated with age and duration of DM1. There was not found any significant relation between TGF-β and parameres of glycation and oxidation. However, these results do not exclude the association between TGF-β and the onset of diabetic complications.
format Online
Article
Text
id pubmed-3463181
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-34631812012-10-04 Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1 Jakuš, Vladimír Sapák, Michal Kostolanská, Jana Exp Diabetes Res Research Article The present study investigates the relationship between diabetes metabolic control represented by levels of HbA1c, early glycation products-(fructosamine (FAM)), serum-advanced glycation end products (s-AGEs), lipoperoxidation products (LPO), advanced oxidation protein products (AOPP) and circulating TGF-β in young patients with DM1. The study group consisted of 79 patients with DM1 (8–18 years). 31 healthy children were used as control (1–16 years). Baseline characteristics of patients were compared by Student's t-test and nonparametric Mann-Whitney test (Statdirect), respectively. The correlations between the measured parameters were examined using Pearson correlation coefficient r and Spearman's rank test, respectively. A P value < 0.05 was considered as statistically significant. HbA1c was measured by LPLC, s-AGEs spectrofluorimetrically, LPO and AOPP spectrophotometrically and TGF-β by ELISA. Our results showed that parameters of glycation and oxidation are significantly higher in patients with DM1 than in healthy control. The level of serum TGF-β was significantly higher in diabetics in comparison with control: 7.1(3.6; 12.6) versus 1.6(0.8; 3.9) ng/mL. TGF-β significantly correlated with age and duration of DM1. There was not found any significant relation between TGF-β and parameres of glycation and oxidation. However, these results do not exclude the association between TGF-β and the onset of diabetic complications. Hindawi Publishing Corporation 2012 2012-09-26 /pmc/articles/PMC3463181/ /pubmed/23049541 http://dx.doi.org/10.1155/2012/510902 Text en Copyright © 2012 Vladimír Jakuš et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jakuš, Vladimír
Sapák, Michal
Kostolanská, Jana
Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1
title Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1
title_full Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1
title_fullStr Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1
title_full_unstemmed Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1
title_short Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1
title_sort circulating tgf-β1, glycation, and oxidation in children with diabetes mellitus type 1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463181/
https://www.ncbi.nlm.nih.gov/pubmed/23049541
http://dx.doi.org/10.1155/2012/510902
work_keys_str_mv AT jakusvladimir circulatingtgfb1glycationandoxidationinchildrenwithdiabetesmellitustype1
AT sapakmichal circulatingtgfb1glycationandoxidationinchildrenwithdiabetesmellitustype1
AT kostolanskajana circulatingtgfb1glycationandoxidationinchildrenwithdiabetesmellitustype1