Antioxidants, oxidative stress, and pulmonary function in individuals diagnosed with asthma or COPD

Eur J Clin Nutr. 2006 Aug;60(8):991-9. doi: 10.1038/sj.ejcn.1602410. Epub 2006 Feb 15.

Abstract

Objective: The objective of this study was to investigate the association between antioxidant nutrients and markers of oxidative stress with pulmonary function in persons with chronic airflow limitation.

Design: Cross-sectional study exploring the association of antioxidant nutrients and markers of oxidative stress with forced expiratory volume in the first second (FEV1%) and forced vital capacity (FVC%).

Setting/subjects: The study data included 218 persons with chronic airflow limitation recruited randomly from the general population of Erie and Niagara counties, New York State, USA.

Results: After adjustment for covariates, multiple linear regression analysis showed that serum beta-cryptoxanthin, lutein/zeaxanthin, and retinol, and dietary beta-carotene, beta-cryptoxanthin, lutein/zeaxanthin, vitamin C, and lycopene were positively associated with FEV1% (P < 0.05, all associations). Serum vitamins beta-cryptoxanthin, lutein/zeaxanthin, and lycopene, and dietary beta-cryptoxanthin, beta-carotene, vitamin C, and lutein/zeaxanthin were positively associated with FVC% (P < 0.05, all associations). Erythrocytic glutathione was negatively associated with FEV1%, while plasma thiobarbituric acid-reactive substances (TBARS) were negatively associated with FVC% (P < 0.05).

Conclusion: These results support the hypothesis that an imbalance in antioxidant/oxidant status is associated with chronic airflow limitation, and that dietary habits and/or oxidative stress play contributing roles.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / administration & dosage*
  • Antioxidants / metabolism
  • Antioxidants / physiology*
  • Asthma / metabolism*
  • Biomarkers / blood
  • Cross-Sectional Studies
  • Forced Expiratory Volume / physiology
  • Glutathione / blood
  • Glutathione Peroxidase / blood
  • Humans
  • Linear Models
  • Multivariate Analysis
  • New York
  • Oxidation-Reduction
  • Oxidative Stress / physiology*
  • Pulmonary Disease, Chronic Obstructive / metabolism*
  • Respiration
  • Respiratory Function Tests
  • Risk Factors
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Vital Capacity / physiology

Substances

  • Antioxidants
  • Biomarkers
  • Thiobarbituric Acid Reactive Substances
  • Glutathione Peroxidase
  • Glutathione