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Soy isoflavones increase preprandial peptide YY (PYY), but have no effect on ghrelin and body weight in healthy postmenopausal women

Martin O Weickert* 1,2 email, Manja Reimann* 1,3 email, Bärbel Otto4 email, Wendy L Hall5 email, Katherina Vafeiadou5 email, Jesper Hallund6 email, Marika Ferrari7 email, Duncan Talbot8 email, Francesco Branca7 email, Susanne Bügel6 email, Christine M Williams5 email, Hans-Joachim Zunft1 email and Corinna Koebnick1,9 email

1German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany

2Dept. of Endocrinology, Diabetes and Nutrition, Charité-University-Medicine, Berlin, Germany

3School for Physiology, Nutrition and Consumer Sciences, North-West University Potchefstroom-Campus, Potchefstroom, South Africa

4Medical Dept., University Hospital Innenstadt, Munich, Germany

5School of Food Biosciences, University of Reading, Reading, UK

6The Royal Veterinary & Agricultural University, Research Dept. of Human Nutrition, Centre for Advanced Food Studies, Frederiksberg, Denmark

7Istituto Nazionale di Ricerca per gli Alimenti e la Nutrizione, Rome, Italy

8Unilever Corporate Research, Colworth House, Sharnbrook, Bedfordshire, UK

9Dept. of Preventive Medicine, University of Southern California, Los Angeles, USA

author email corresponding author email* Contributed equally

Journal of Negative Results in BioMedicine 2006, 5:11doi:10.1186/1477-5751-5-11

Published: 14 August 2006

Abstract

Background

Soy isoflavones show structural and functional similarities to estradiol. Available data indicate that estradiol and estradiol-like components may interact with gut "satiety hormones" such as peptide YY (PYY) and ghrelin, and thus influence body weight. In a randomized, double-blind, placebo-controlled, cross-over trial with 34 healthy postmenopausal women (59 ± 6 years, BMI: 24.7 ± 2.8 kg/m2), isoflavone-enriched cereal bars (50 mg isoflavones/day; genistein to daidzein ratio 2:1) or non-isoflavone-enriched control bars were consumed for 8 weeks (wash-out period: 8-weeks). Seventeen of the subjects were classified as equol producers. Plasma concentrations of ghrelin and PYY, as well as energy intake and body weight were measured at baseline and after four and eight weeks of each intervention arm.

Results

Body weight increased in both treatment periods (isoflavone: 0.40 ± 0.94 kg, P < 0.001; placebo: 0.66 ± 0.87 kg, P = 0.018), with no significant difference between treatments. No significant differences in energy intake were observed (P = 0.634). PYY significantly increased during isoflavone treatment (51 ± 2 pmol/L vs. 55 ± 2 pmol/L), but not during placebo (52 ± 3 pmol/L vs. 50 ± 2 pmol/L), (P = 0.010 for treatment differences, independent of equol production). Baseline plasma ghrelin was significantly lower in equol producers (110 ± 16 pmol/L) than in equol non-producers (162 ± 17 pmol/L; P = 0.025).

Conclusion

Soy isoflavone supplementation for eight weeks did not significantly reduce energy intake or body weight, even though plasma PYY increased during isoflavone treatment. Ghrelin remained unaffected by isoflavone treatment. A larger and more rigorous appetite experiment might detect smaller differences in energy intake after isoflavone consumption. However, the results of the present study do not indicate that increased PYY has a major role in the regulation of body weight, at least in healthy postmenopausal women.


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