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Lipids and cardiovascular/metabolic health

Red clover isoflavones enriched with formononetin lower serum LDL cholesterol—a randomized, double-blind, placebo-controlled study

Abstract

Background:

Although postmenopausal combined hormone replacement therapy reduces the risk of hip fracture, long-term use may be associated with an increased risk of breast cancer, and in women more than 10 years after menopause it is associated with an increased risk of cardiovascular disease. Isoflavones, because of preferential binding to estrogen receptor beta, may retain the beneficial effects on bone but lessen the adverse effects on the breast.

Objective:

The objective of this study was to study the effects of an isoflavone obtained from red clover (Rimostil) on bone mineral density, and on low-density lipoprotein (LDL) cholesterol.

Design:

In a double-blind, randomized, placebo-controlled trial, 50 mg of Rimostil was given to women who were menopausal for at least 1 year. Bone mineral density of the spine, femoral neck and forearm and serum LDL cholesterol were measured at baseline and at 6-month intervals. The duration of follow-up was 2 years.

Results:

There was no beneficial effect of Rimostil on bone density at any site. There was a 12% fall in serum LDL cholesterol in the Rimostil-treated arm, which was significantly greater than the 2% drop seen in the control arm (P=0.005).

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Acknowledgements

Study medication used in the trial was supplied by Novogen Ltd. The cost of the biochemical testing was met by Novogen Ltd.

Disclaimer

A partial professional salary was paid to MLN, the study coordinator who recruited and supervised all study participants. None of the other authors received any payment from Novogen Ltd. None of the authors or members of their families hold any stock in Novogen Ltd. This double-blind, placebo-controlled study was not registered with the clinical trials registry because the study commenced before the requirement was introduced to register all clinical trials.

Author contributions

PBC-B, GRF and RB developed the overall research plan and designed the protocol. MLN was responsible for participant recruitment and for the progress of each participant through the study protocol to the time of completion or withdrawal. PBC-B, RJC-B, SV, GRF and RB were responsible for ongoing clinical assessment of each participant throughout the trial. PBC-B and KB made major contributions to the writing of the manuscript and take responsibility for the validity of the data. KB performed statistical analyses of the data. SV died during the course of the study. All other authors have read and approved the final manuscript.

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Correspondence to P B Clifton-Bligh.

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Clifton-Bligh, P., Nery, ML., Clifton-Bligh, R. et al. Red clover isoflavones enriched with formononetin lower serum LDL cholesterol—a randomized, double-blind, placebo-controlled study. Eur J Clin Nutr 69, 134–142 (2015). https://doi.org/10.1038/ejcn.2014.207

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