Plasma selenium levels and oxidative stress biomarkers: A gene–environment interaction population-based study

The role of selenium exposure in preventing chronic disease is controversial, especially in selenium-repleted populations. At high concentrations, selenium exposure may increase oxidative stress. Studies evaluating the interaction of genetic variation in genes involved in oxidative stress pathways a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Free radical biology & medicine 2014-09, Vol.74, p.229-236
Hauptverfasser: Galan-Chilet, Inmaculada, Tellez-Plaza, Maria, Guallar, Eliseo, De Marco, Griselda, Lopez-Izquierdo, Raul, Gonzalez-Manzano, Isabel, Carmen Tormos, M., Martin-Nuñez, Gracia M., Rojo-Martinez, Gemma, Saez, Guillermo T., Martín-Escudero, Juan C., Redon, Josep, Javier Chaves, F.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The role of selenium exposure in preventing chronic disease is controversial, especially in selenium-repleted populations. At high concentrations, selenium exposure may increase oxidative stress. Studies evaluating the interaction of genetic variation in genes involved in oxidative stress pathways and selenium are scarce. We evaluated the cross-sectional association of plasma selenium concentrations with oxidative stress levels, measured as oxidized to reduced glutathione ratio (GSSG/GSH), malondialdehyde (MDA), and 8-oxo-7,8-dihydroguanine (8-oxo-dG) in urine, and the interacting role of genetic variation in oxidative stress candidate genes, in a representative sample of 1445 men and women aged 18–85 years from Spain. The geometric mean of plasma selenium levels in the study sample was 84.76µg/L. In fully adjusted models the geometric mean ratios for oxidative stress biomarker levels comparing the highest to the lowest quintiles of plasma selenium levels were 0.61 (0.50–0.76) for GSSG/GSH, 0.89 (0.79–1.00) for MDA, and 1.06 (0.96–1.18) for 8-oxo-dG. We observed nonlinear dose–responses of selenium exposure and oxidative stress biomarkers, with plasma selenium concentrations above ~110μg/L being positively associated with 8-oxo-dG, but inversely associated with GSSG/GSH and MDA. In addition, we identified potential risk genotypes associated with increased levels of oxidative stress markers with high selenium levels. Our findings support that high selenium levels increase oxidative stress in some biological processes. More studies are needed to disentangle the complexity of selenium biology and the relevance of potential gene–selenium interactions in relation to health outcomes in human populations. •Reported adverse effects of selenium excess may be explained by oxidative stress.•Elevated selenium was positively associated with 8-oxo-dG, but not GSSG/GSH and MDA.•Certain genotypes showed higher oxidative stress marker levels with high selenium.•Our results support that selenium and genetic variation interact to alter redox state.•Research to evaluate gene–selenium interaction in relation to human health is needed.
ISSN:0891-5849
1873-4596
DOI:10.1016/j.freeradbiomed.2014.07.005