Table 4. Associations between tertiles of dietary iron intake and breast cancer risk from multivariable cox proportional hazards models, stratified by antioxidant/placebo group of the SU.VI.MAX trial and by lipid intake,france, 1994–@2007a, b, c.
Placebo group | Antioxidant supplementation group | |||||
---|---|---|---|---|---|---|
N for cases/non-cases | HR (95% CI) | P-trend | N for cases/non-cases | HR (95% CI) | P-trend | |
Total lipid intake < median (78.5 g/d) | 0.1 | 0.3 | ||||
Tertile 1 | 20/632 | 1.00 | 21/602 | 1.00 | ||
Tertile 2 | 18/338 | 1.58 (0.76, 3.24) | 12/345 | 0.94 (0.41, 2.15) | ||
Tertile 3 | 12/143 | 1.99 (0.79, 4.99) | 11/169 | 1.67 (0.63, 4.42) | ||
Total lipid intake ≥ median (78.5 g/d) | 0.046 | 0.2 | ||||
Tertile 1 | 5/140 | 1.00 | 7/121 | 1.00 | ||
Tertile 2 | 15/413 | 1.41 (0.49, 4.06) | 12/396 | 0.40 (0.15, 1.05) | ||
Tertile 3 | 30/576 | 2.57 (0.86, 7.68) | 25/583 | 0.42 (0.15, 1.17) |
CI, confidence interval, HR, Hazard ratio, SU.VI.MAX, Supplémentation en Vitamines et Minéraux Antioxydants
Multivariable models were adjusted for age (timescale), energy intake without alcohol, intervention group of the initial SU.VI.MAX trial, number of 24-h dietary records, smoking status, educational level, physical activity, height, BMI, alcohol intake, family history of breast cancer, lipids intake, use of hormone replacement therapy, and number of children.
b Cut-offs for tertiles of dietary iron intake were 9.3 and 11.9 mg/d.
c P for interaction between dietary iron and lipid intakes: Placebo group, 0.3; Antioxidant supplementation group, 0.5.