Relationship between oxidative stress and muscle mass loss in early postmenopause: an exploratory study

Endocrinol Diabetes Nutr (Engl Ed). 2018 Jun-Jul;65(6):328-334. doi: 10.1016/j.endinu.2018.01.009. Epub 2018 Apr 9.
[Article in English, Spanish]

Abstract

Background: Endocrine changes due to menopause have been associated to oxidative stress and muscle mass loss. The study objective was to determine the relationship between both variables in early postmenopause.

Material and methods: An exploratory, cross-sectional study was conducted in 107 pre- and postmenopausal women (aged 40-57 years). Levels of serum lipid peroxides and uric acid and enzymes superoxide dismutase and glutathione peroxidase, as well as total plasma antioxidant capacity were measured as oxidative stress markers. Muscle mass using bioelectrical impedance and muscle strength using dynamometry were also measured. Muscle mass, skeletal muscle index, fat-free mass, and body mass index were calculated.

Results: More than 90% of participants were diagnosed with overweight or obesity. Postmenopausal women had lower values of muscle mass and strength markers, with a negative correlation between lipid peroxide level and skeletal muscle index (r= -0.326, p<.05), and a positive correlation between uric acid and skeletal muscle index (r=0.295, p<.05). A multivariate model including oxidative stress markers, age, and waist circumference showed lipid peroxide level to be the main contributor to explain the decrease in skeletal muscle mass in postmenopause, since for every 0.1μmol/l increase in lipid peroxide level, skeletal muscle index decreases by 3.03 units.

Conclusion: Our findings suggest an association between increased oxidative stress and muscle mass loss in early postmenopause.

Keywords: Estrés oxidativo; Lipid peroxide; Lipoperóxido; Masa muscular; Muscle mass; Oxidative stress; Posmenopausia; Postmenopause; Sarcopenia.

MeSH terms

  • Adult
  • Cross-Sectional Studies
  • Female
  • Humans
  • Middle Aged
  • Oxidative Stress*
  • Postmenopause / metabolism*
  • Sarcopenia / metabolism*