Table 2.
Isoflavone intake and breast cancer risk in low-consuming populations
| Authors [Ref.] | Study design | Subjects, n | Results (95% CI) | Comments |
|---|---|---|---|---|
| Wu et al. [35] | meta-analysis of 11 studies (7 case-control, 4 cohort) | 8,533 cases, 8596 controls; cohort of 170,693 women | OR 1.04 (0.97–1.11) | ≥ 0.8 mg vs. 0.15 mg daily isoflavone intake |
| only case-control studies | 6807 cases, 8596 controls | OR 1.02 (0.95–1.11) | ||
| only cohort studies | 1726 cases; cohort of 170,693 women | OR 1.08 (0.95–1.24) | ||
| Cutler et al. [39] | cohort study | 2,529 cases; cohort of 34,708 postmenopausal women | not available | ≥ 0.52 mg vs. ≤ 0.13 mg daily isoflavone intake; no significant difference for isoflavone intake |
| Hedelin et al. [40] | cohort study | 1,014 cases; cohort of 45,448 women | RR 0.98 (0.83–1.17) | highest vs. lowest quartile of isoflavone intake (< 0.1 mg/day) |
| Travis et al. [41] | cohort study | 585 cases; cohort of 37,643 women | HR 1.17 (0.79–1.71) | ≥ 20 mg vs. < 10 mg daily isoflavone intake; only 29 cases with intake ≥ 20 mg |
| Ward et al. [42] | nested case-control study | 237 cases, 952 controls out of 14,032 women | OR 1.08 (1.00–1.06) | high vs. low levels of urine isoflavones, results are inconsistent with the nonsignificant difference of isoflavone plasma levels |
| Verheus et al. [43] | nested case-control study | 383 cases, 383 controls | OR 0.68 (0.47–0.98) | highest vs. lowest tertile of plasma levels of genistein, effect is stronger in postmenopausal women |
CI = Confidence interval; OR = odds ratio; RR = risk ratio; HR = hazard ratio.