Abstract
Background: Glutathione S-transferase (GST) enzymes are critical for detoxifying reactive oxygen species (ROS) and their products which have been implicated in the pathology of inflammatory diseases such as atopic dermatitis (AD). Methods: We investigated the effects of genetic polymorphisms of GST on the risk of AD in preschool age children. Biomarkers for oxidative stress were also evaluated with respect to GST genotype. Results: The GSTP1 Val105 allele was significantly associated with an increased risk of AD [odds ratio (OR)=1.62, p<0.05]. The combination of the GSTP1 Val105 allele and the GSTT1 null genotype further increased this risk by 2.3-fold (p<0.01). No association was observed for the GSTM1 null or GSTT1 null genotype alone. In children with AD, blood total antioxidant capacity was significantly less (p<0.001), while malondialdehyde was higher (p=0.12). Children with the GSTP1 Val105 allele had significantly lower concentrations of erythrocyte glutathione compared to GSTP1 Ile/Ile homozygotes (p=0.03). Conclusions: Our study suggests that the GSTP1 Val105 allele is an important determinant of susceptibility to AD in preschool age children and increased oxidative stress may play a role in the pathogenesis of AD.
Original language | English |
---|---|
Pages (from-to) | 1475-1481 |
Number of pages | 7 |
Journal | Clinical Chemistry and Laboratory Medicine |
Volume | 47 |
Issue number | 12 |
DOIs | |
Publication status | Published - 2009 |
Bibliographical note
Funding Information:The present study was supported by grant No. R01-2006-000-10887-0 from the Basic Research Program of the Korea Science & Engineering Foundation.
Keywords
- Atopic dermatitis
- Glutathione-S-transferase
- Oxidative stress
- Polymorphism
- Preschool age children