Urinary 2- to 16α-hydroxyestrone ratio did not change with cruciferous vegetable intake in premenopausal women.

Stephanie J Davis, Sara A Arscott, Shellen Goltz, Cassidy Muir, Neil Binkley, Sherry A Tanumihardjo

Journal: International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition 2024;94(3-4):177-186

PMID: 37335576

Abstract

The mass ratio of urinary 2-hydroxyestrone to 16-α-hydroxyestrone (2:16) is hypothesized as a biomarker of breast cancer risk in premenopausal women, with higher ratios being theoretically protective. Cruciferous vegetable intake has been associated with higher urinary 2:16 in some studies. We investigated whether a whole-food supplement made from dried Brussels sprouts and kale would increase urinary 2:16 in comparison with placebo or cruciferous vegetables in women. This randomized, parallel arm, placebo-controlled, partly blinded study included 78 healthy premenopausal women (38-50 y) with screening urinary 2:16 ≤3.0. Subjects received either six capsules containing 550 mg dried Brussels sprouts and kale per capsule, 40 g daily alternating broccoli or Brussels sprouts, or placebo for eight weeks. Urinary 2:16 and creatinine were measured at baseline, four, and eight weeks. Intent-to-treat repeated measures-ANOVA with multiple imputation (=100) for missing values identified no treatment effect (=0.9) or treatment-by-time interaction (=0.6); however, a significant time effect was noted (=0.02). Per-protocol analyses including complete cases found no treatment effect (=1) or treatment-by-time interaction (=0.6); however, the significant time effect remained (=0.03). Restricting analysis to subjects with >80% compliance maintained the time effect (=0.02). Using Pearson correlations, android-pattern and android:gynoid fat were predictive of change (≤0.05). In conclusion, neither cruciferous supplements nor an added vegetable serving altered urinary 2:16 in premenopausal women with eight weeks treatment. This ratio did vary with time, which is important for designing future trials.

Address: Interdepartmental Graduate Program in Nutritional Sciences, University of Wisconsin-Madison (UW), Madison, USA.; Standard Process Inc., Palmyra, Wisconsin, USA.; Department of Family Medicine and Community Health, University of Wisconsin-Madison (UW), Madison, USA.; Osteoporosis Clinical Research Program, University of Wisconsin-Madison (UW), Madison, USA.

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