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Trace elements and oxidative stress in children with type 1 diabetes mellitus
BACKGROUND: The early imbalances of trace elements in type 1 diabetes (T1D) may cause disturbance of glucose metabolism and more oxidative stress that may enhance the development of insulin resistance and diabetic complications. We aim to evaluate the serum level of selenium (Se), zinc (Zn), magnesi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875397/ https://www.ncbi.nlm.nih.gov/pubmed/29618936 http://dx.doi.org/10.2147/DMSO.S157348 |
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author | Alghobashy, Ashgan Abdalla Alkholy, Usama M Talat, Mohamed A Abdalmonem, Nermin Zaki, Ahmed Ahmed, Ihab A Mohamed, Randa H |
author_facet | Alghobashy, Ashgan Abdalla Alkholy, Usama M Talat, Mohamed A Abdalmonem, Nermin Zaki, Ahmed Ahmed, Ihab A Mohamed, Randa H |
author_sort | Alghobashy, Ashgan Abdalla |
collection | PubMed |
description | BACKGROUND: The early imbalances of trace elements in type 1 diabetes (T1D) may cause disturbance of glucose metabolism and more oxidative stress that may enhance the development of insulin resistance and diabetic complications. We aim to evaluate the serum level of selenium (Se), zinc (Zn), magnesium (Mg), and copper (Cu), the degree of oxidative stress and evaluate their relations to glycemic control in children with T1D. METHODS: A case–control study which included 100 diabetic children and 40 healthy children age, sex, and ethnicity-matched as a control group. The diabetic children were divided into poor and good controlled patients according to glycosylated hemoglobin (A1c %). Studied children underwent history taking, clinical examination and laboratory measurement of serum Se, Zn, Mg, and Cu levels, erythrocyte reduced glutathione (GSH) and peroxidase enzyme activity (GPx). RESULTS: Serum Se, Zn, Mg, Cu, erythrocyte GSH, and GPx were significantly lower in the diabetic group in comparison to the control group (P<0.05) and their levels were lower in poorly controlled patients compared to good controlled patients (P<0.05). The serum Se, Zn, Mg, erythrocyte GSH, and GPx showed a negative correlation with A1c %. The serum Se showed a positive correlation with erythrocyte GSH and GPx ([r=0.56, P<0.001], [r=0.78, P<0.001], respectively). CONCLUSION: Children with T1D, especially poorly controlled cases, had low serum Se, Zn, Mg, Cu, GSH, and GPx. Low serum Se in diabetic children may affect the erythrocyte GSH-GPx system. |
format | Online Article Text |
id | pubmed-5875397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58753972018-04-04 Trace elements and oxidative stress in children with type 1 diabetes mellitus Alghobashy, Ashgan Abdalla Alkholy, Usama M Talat, Mohamed A Abdalmonem, Nermin Zaki, Ahmed Ahmed, Ihab A Mohamed, Randa H Diabetes Metab Syndr Obes Original Research BACKGROUND: The early imbalances of trace elements in type 1 diabetes (T1D) may cause disturbance of glucose metabolism and more oxidative stress that may enhance the development of insulin resistance and diabetic complications. We aim to evaluate the serum level of selenium (Se), zinc (Zn), magnesium (Mg), and copper (Cu), the degree of oxidative stress and evaluate their relations to glycemic control in children with T1D. METHODS: A case–control study which included 100 diabetic children and 40 healthy children age, sex, and ethnicity-matched as a control group. The diabetic children were divided into poor and good controlled patients according to glycosylated hemoglobin (A1c %). Studied children underwent history taking, clinical examination and laboratory measurement of serum Se, Zn, Mg, and Cu levels, erythrocyte reduced glutathione (GSH) and peroxidase enzyme activity (GPx). RESULTS: Serum Se, Zn, Mg, Cu, erythrocyte GSH, and GPx were significantly lower in the diabetic group in comparison to the control group (P<0.05) and their levels were lower in poorly controlled patients compared to good controlled patients (P<0.05). The serum Se, Zn, Mg, erythrocyte GSH, and GPx showed a negative correlation with A1c %. The serum Se showed a positive correlation with erythrocyte GSH and GPx ([r=0.56, P<0.001], [r=0.78, P<0.001], respectively). CONCLUSION: Children with T1D, especially poorly controlled cases, had low serum Se, Zn, Mg, Cu, GSH, and GPx. Low serum Se in diabetic children may affect the erythrocyte GSH-GPx system. Dove Medical Press 2018-03-26 /pmc/articles/PMC5875397/ /pubmed/29618936 http://dx.doi.org/10.2147/DMSO.S157348 Text en © 2018 Alghobashy et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Alghobashy, Ashgan Abdalla Alkholy, Usama M Talat, Mohamed A Abdalmonem, Nermin Zaki, Ahmed Ahmed, Ihab A Mohamed, Randa H Trace elements and oxidative stress in children with type 1 diabetes mellitus |
title | Trace elements and oxidative stress in children with type 1 diabetes mellitus |
title_full | Trace elements and oxidative stress in children with type 1 diabetes mellitus |
title_fullStr | Trace elements and oxidative stress in children with type 1 diabetes mellitus |
title_full_unstemmed | Trace elements and oxidative stress in children with type 1 diabetes mellitus |
title_short | Trace elements and oxidative stress in children with type 1 diabetes mellitus |
title_sort | trace elements and oxidative stress in children with type 1 diabetes mellitus |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875397/ https://www.ncbi.nlm.nih.gov/pubmed/29618936 http://dx.doi.org/10.2147/DMSO.S157348 |
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