Age-related sex differences in glutathione peroxidase and oxidative DNA damage in a healthy Mexican population

J Womens Health (Larchmt). 2010 May;19(5):919-26. doi: 10.1089/jwh.2009.1684.

Abstract

Background and objective: It has been proposed that women have an estrogen activity-linked biological antioxidant advantage and that this advantage is lost in the postmenopausal stage. The latter remains controversial. Our aim was to determine age-related sex differences in oxidative stress and oxidative DNA damage in a healthy Mexican population.

Methods: A cross-sectional and comparative study was carried out in a convenience sample of 162 healthy subjects aged as follows: (1) 25-44 years (n = 35 women and 38 men), (2) 45-64 years (n = 41 women and 27 men), and (3) >or=65 years (n = 13 women and 8 men). We measured plasma lipoperoxides (LPO), superoxide dismutase (SOD), glutathione peroxidase (GPx), and DNA damage by comet assay.

Results: We found greater activity of GPx in women than in men according to age increase (p < 0.05). This activity is maintained in old age in women. In contrast, men exhibited a significant diminution in GPx according to age increase. Similarly, we observed a greater percentage of cells without oxidative DNA damage in women in the 45-64-years age group and in the group of women aged >or=65 years.

Conclusions: Our findings suggest that women have a more efficient antioxidant activity than men, which has been linked with the greater longevity observed in women.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age Factors
  • Comet Assay
  • Cross-Sectional Studies
  • DNA Damage*
  • Female
  • Glutathione Peroxidase / blood*
  • Humans
  • Lipid Peroxides / blood*
  • Male
  • Mexico
  • Middle Aged
  • Oxidative Stress / physiology*
  • Sex Factors
  • Smoking
  • Superoxide Dismutase / blood*
  • Surveys and Questionnaires
  • Thiobarbituric Acid Reactive Substances / analysis
  • Young Adult

Substances

  • Lipid Peroxides
  • Thiobarbituric Acid Reactive Substances
  • Glutathione Peroxidase
  • Superoxide Dismutase