Selenium inadequacy is not associated with oxidative stress in child and adolescent acute lymphocytic leukemia survivors

Nutrition. 2014 May;30(5):563-8. doi: 10.1016/j.nut.2013.10.012. Epub 2013 Oct 30.

Abstract

Objective: Acute lymphocytic leukemia (ALL) and its subsequent treatment may provoke increased oxidative stress. The aim of this study was to investigate the antioxidant status of children and adolescents who had received ALL therapy, and to test the hypothesis that selenium (Se) inadequacy is correlated with reduced defenses against oxidative stress in this population.

Methods: This case-control study involved 24 patients between ages 5 and 13 y who had been treated successfully for ALL (ALL group) and 60 children of similar age and socioeconomic background with no clinical history of leukemia (control group). Dietary intake of Se was evaluated by the 24-h recall method, and the concentrations of Se in plasma, erythrocytes, and urine determined. Antioxidant status was assessed by analysis of the oxidative stress markers, namely, superoxide dismutase (SOD), glutathione peroxidase (GPx), malondialdehyde (MDA), α-tocopherol, and 8-oxo-deoxyguanosine (8-oxo-dG).

Results: There were no between-group differences with respect to plasma (P = 0.122), erythrocyte (P = 0.202), urinary (P = 0.608), or dietary (P = 0.757) levels of Se. GPx activity was significantly (P < 0.001) reduced in the ALL group compared with the control group, whereas SOD activity and MDA concentrations were similar. The concentrations of α-tocopherol and 8-oxo-dG were significantly increased in the ALL group compared with the control group (P < 0.001 and P = 0.031, respectively).

Conclusion: All participants were Se inadequate, but such inadequacy was not correlated with reduced defenses against oxidative stress. However, individuals of the ALL group were with increased oxidative stress compared with the control group, possibly due to previous disease and to intensive polychemotherapy.

Keywords: Acute lymphoblastic leukemia; Antioxidants; Chemotherapy; DNA damage; Oxidative stress; Selenium.

MeSH terms

  • Adolescent
  • Antioxidants / metabolism*
  • Biomarkers / metabolism
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Deficiency Diseases / complications*
  • Deficiency Diseases / metabolism
  • Deoxyguanosine / blood
  • Erythrocytes / metabolism
  • Female
  • Glutathione Peroxidase / metabolism
  • Humans
  • Lipid Peroxidation
  • Male
  • Malondialdehyde / blood
  • Oxidative Stress*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / complications
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / metabolism*
  • Selenium / blood
  • Selenium / deficiency*
  • Selenium / urine
  • Superoxide Dismutase / metabolism
  • Survivors
  • alpha-Tocopherol / blood

Substances

  • Antioxidants
  • Biomarkers
  • Malondialdehyde
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Deoxyguanosine
  • alpha-Tocopherol
  • Selenium