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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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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 |
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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 |
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