Authors: Ho, S, Hui, E, Li, H, Wong, ELY, Wong, WCW, Woo, J, You, JH
Published: January 1, 2012
In this 12-month double-blind, randomized, placebo-controlled trial of 176 men with BPH in Hong Kong, participants received either 40mg daily soy isoflavones or placebo. Peak urine flow rate (Qmax) showed marginal difference between groups (p=0.055) from months 6-12. The incomplete bladder emptying subscore in International Prostate Symptoms Scores (IPSS) reached borderline statistical significance (p=0.05) during the same period. The general health domain of SF-36 quality of life showed significant improvement in the isoflavone group versus placebo from baseline to 12 months (p=0.02). Both groups showed within-group improvements in Qmax, post-void residual volume, IPSS, and SF-36 scores. Isoflavones demonstrated excellent tolerability with no significant adverse effects on liver function, renal function, testosterone, or prostate-specific antigen levels.
