Parameters of oxidative stress in children with Type 1 diabetes mellitus and their relatives
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
12505749
DOI
10.1016/s1056-8727(01)00228-8
PII: S1056872701002288
Knihovny.cz E-zdroje
- MeSH
- antioxidancia analýza MeSH
- autoprotilátky krev MeSH
- diabetes mellitus 1. typu imunologie patofyziologie MeSH
- dítě MeSH
- dospělí MeSH
- erytrocyty chemie enzymologie MeSH
- glutamát dekarboxyláza imunologie MeSH
- glutathion krev MeSH
- glutathionperoxidasa krev MeSH
- lidé MeSH
- malondialdehyd krev MeSH
- mladiství MeSH
- oxidace-redukce MeSH
- oxidační stres * MeSH
- předškolní dítě MeSH
- rodiče MeSH
- sourozenci MeSH
- superoxiddismutasa krev MeSH
- volné radikály krev MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- antioxidancia MeSH
- autoprotilátky MeSH
- glutamát dekarboxyláza MeSH
- glutathion MeSH
- glutathionperoxidasa MeSH
- islet cell antibody MeSH Prohlížeč
- malondialdehyd MeSH
- superoxiddismutasa MeSH
- volné radikály MeSH
Oxidative stress (OS) plays an important role in the pathogenesis of Type 1 diabetes mellitus (DM). The aim of the study was to compare OS parameters in diabetic children and their first-degree relatives. Fifty diabetic children from the West Bohemian Region were examined as well as their 32 siblings (12 Boys and 20 girls) and 65 of their parents during a period of 6 months. Thirty healthy sex- and age-matched children studied before planned surgeries were normal controls for children, 40 healthy adult volunteers were controls for parents. OS parameters were evaluated in all participants of the study (superoxide dismutase, SOD; glutathione peroxidase, GSHPx; plasma antioxidant capacity, AOC; reduced glutathione, GSH; and malondialdehyde, MDA) and also Type 1 DM-associated antibodies (ICA and GADA). The results in diabetic children showed significantly lower GSHPx and AOC and increased MDA when compared with healthy children. Similar findings were found in their siblings but without statistical significance. It is consequently evident that decreased antioxidative protection and simultaneous free radical (FR) overproduction occur in diabetic children and that there is a similar, but not significant, tendency in their siblings. The findings warrant reducing OS in diabetic children and postponing disease onset in susceptible relatives.
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