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Published in: Breast Cancer Research 3/2004

Open Access 01-06-2004 | Research article

Red clover-derived isoflavones and mammographic breast density: a double-blind, randomized, placebo-controlled trial [ISRCTN42940165]

Authors: Charlotte Atkinson, Ruth ML Warren, Evis Sala, Mitch Dowsett, Alison M Dunning, Catherine S Healey, Shirley Runswick, Nicholas E Day, Sheila A Bingham

Published in: Breast Cancer Research | Issue 3/2004

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Abstract

Introduction

Isoflavones are hypothesized to protect against breast cancer, but it is not clear whether they act as oestrogens or anti-oestrogens in breast tissue. Our aim was to determine the effects of taking a red clover-derived isoflavone supplement daily for 1 year on mammographic breast density. Effects on oestradiol, follicle-stimulating hormone (FSH), luteinizing hormone (LH), lymphocyte tyrosine kinase activity and menopausal symptoms were also assessed.

Methods

A total of 205 women (age range 49–65 years) with Wolfe P2 or DY mammographic breast patterns were randomly assigned to receive either a red clover-derived isoflavone tablet (26 mg biochanin A, 16 mg formononetin, 1 mg genistein and 0.5 mg daidzein) or placebo. Change in mammographic breast density, serum oestradiol, FSH, LH, menopausal symptoms and lymphocyte tyrosine kinase activity from baseline to 12 months were assessed.

Results

A total of 177 women completed the trial. Mammographic breast density decreased in both groups but the difference between the treatment and placebo was not statistically significant. There was a significant interaction between treatment group and oestrogen receptor (ESR1) PvuII polymorphism for the change in estimated percentage breast density (mean ± standard deviation): TT isoflavone 1.4 ± 12.3% and TT placebo -9.6 ± 14.2%; CT isoflavone -5.2 ± 12.0% and CT placebo -2.8 ± 10.3%; and CC isoflavone -3.4 ± 9.7% and CC placebo -1.1 ± 9.5%. There were no statistically significant treatment effects on oestradiol, FSH, or LH (assessed only in postmenopausal women), or on lymphocyte tyrosine kinase activity. Baseline levels of menopausal symptoms were low, and there were no statistically significant treatment effects on frequency of hot flushes or other menopausal symptoms.

Conclusion

In contrast to studies showing that conventional hormone replacement therapies increase mammographic breast density, the isoflavone supplement did not increase mammographic breast density in this population of women. Furthermore, there were no effects on oestradiol, gonadotrophins, lymphocyte tyrosine kinase activity, or menopausal symptoms.
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go back to reference All authors participated fully in the manuscript preparation. In addition, individual authors were involved in the following aspects of the trial: Charlotte Atkinson, recruitment and day-to-day running of the trial, sample analyses, and statistical analyses; Ruth ML Warren, breast density; Evis Sala, breast density; Mitch Dowsett, hormone assays; Alison M Dunning, genotyping; Catherine S Healey, genotyping, Shirley Runswick, tyrosine kinase assay; Nicholas E Day, data analysis; Sheila A Bingham, experiment design, sample analysis, and significant advice and consultation regarding all aspects of the trial. All authors participated fully in the manuscript preparation. In addition, individual authors were involved in the following aspects of the trial: Charlotte Atkinson, recruitment and day-to-day running of the trial, sample analyses, and statistical analyses; Ruth ML Warren, breast density; Evis Sala, breast density; Mitch Dowsett, hormone assays; Alison M Dunning, genotyping; Catherine S Healey, genotyping, Shirley Runswick, tyrosine kinase assay; Nicholas E Day, data analysis; Sheila A Bingham, experiment design, sample analysis, and significant advice and consultation regarding all aspects of the trial.
Metadata
Title
Red clover-derived isoflavones and mammographic breast density: a double-blind, randomized, placebo-controlled trial [ISRCTN42940165]
Authors
Charlotte Atkinson
Ruth ML Warren
Evis Sala
Mitch Dowsett
Alison M Dunning
Catherine S Healey
Shirley Runswick
Nicholas E Day
Sheila A Bingham
Publication date
01-06-2004
Publisher
BioMed Central
Published in
Breast Cancer Research / Issue 3/2004
Electronic ISSN: 1465-542X
DOI
https://doi.org/10.1186/bcr773

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