Abstract
Purpose: The cellular oxidative stress (balance between pro-oxidant and antioxidant) may be a major risk factor for chronic diseases. Antioxidant capacity of human diet can be globally assessed through the dietary non-enzymatic antioxidant capacity (NEAC). Our aim was to investigate the relationship between the NEAC and all-cause and cause-specific mortality, and to test potential interactions with smoking status, a well-known pro-oxidant factor. Methods: Among the French women of the E3N prospective cohort study initiated in 1990, including 4619 deaths among 1,199,011 persons-years of follow-up. A validated dietary history questionnaire assessed usual food intake; NEAC intake was estimated using a food composition table from two different methods: ferric ion reducing antioxidant power (FRAP) and total radical-trapping antioxidant parameter (TRAP). Hazard ratio (HR) estimates and 95 % confidence intervals (CI) were derived from Cox proportional hazards regression models. Results: In multivariate analyses, FRAP dietary equivalent intake was inversely associated with mortality from all-causes (HR for the fourth vs. the first quartile: HR4 = 0.75, 95 % CI 0.67, 0.83, ptrend < 0.0001), cancer, and cardiovascular diseases. Similar results were obtained with TRAP. There was an interaction between NEAC dietary equivalent intake and smoking status for all-cause and cardiovascular disease mortality, but not cancer mortality (respectively, for FRAP, pinter = 0.002; 0.013; 0.113, results were similar with TRAP), and the association was the strongest among current smokers. Conclusion: This prospective cohort study highlights the importance of antioxidant consumption for mortality prevention, especially among current smokers.
| Original language | English |
|---|---|
| Pages (from-to) | 1233-1243 |
| Number of pages | 11 |
| Journal | European Journal of Nutrition |
| Volume | 56 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 1 Apr 2017 |
| Externally published | Yes |
Keywords
- All-cause and cause-specific mortality
- E3N study
- FRAP
- Non-enzymatic antioxidant capacity
- TRAP
Fingerprint
Dive into the research topics of 'Dietary antioxidant capacity and all-cause and cause-specific mortality in the E3N/EPIC cohort study'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver