TY - JOUR
T1 - An extract of ganoderma lucidum in men with lower urinary tract symptoms
T2 - A double-blind, placebo-controlled randomized and dose-ranging study
AU - Noguchi, Masanori
AU - Tomiyasu, Katsuro
AU - Nakiri, Makoto
AU - Matsuoka, Kei
AU - Kakuma, Tatsuyuki
AU - Konishi, Fumiko
AU - Kumamoto, Shoichiro
AU - Shimizu, Kuniyoshi
AU - Kondo, Ryuichiro
PY - 2008/9
Y1 - 2008/9
N2 - An ethanol extract of Ganoderma lucidum (G. lucidum) which is an edible and medicinal mushroom shows 5 α-reductase inhibitory activity. A double-blind, placebo-controlled randomized and dose-ranging study was conducted to evaluate the safety and efficacy of the extract of G. lucidum in men with lower urinary tract symptoms (LUTS). We enrolled male volunteers (≥50 yr) with an International Prostate Symptom Score (I-PSS; questions 1-7) ≥ 5 and a prostate-specific antigen (PSA) value < 4 ng/ml. Volunteers were randomized into four groups, of placebo (n= 12), and G. lucidum of 0.6 mg (n = 12), 6 mg (n=12) or 60 mg (n=14), administered once daily. Efficacy was measured as a change from baseline in I-PSS and the peak urine flow rate (Qmax). Prostate volume and residual urine were estimated by ultrasonography, and blood tests, including PSA levels, were also measured at baseline and at the end of the treatment. The overall administration was well tolerated, with no major adverse effects. Statistical significances in the magnitude of changes between the experimental groups were observed at week 4 and week 8. No changes were observed with respect to Qmax, residual urine, prostate volume or/and PSA levels. The extract of G. lucidum was well tolerated and an improvement in I-PSS was observed. The recommended dose of the extract of G. lucidum is 6 mg in men with LUTS.
AB - An ethanol extract of Ganoderma lucidum (G. lucidum) which is an edible and medicinal mushroom shows 5 α-reductase inhibitory activity. A double-blind, placebo-controlled randomized and dose-ranging study was conducted to evaluate the safety and efficacy of the extract of G. lucidum in men with lower urinary tract symptoms (LUTS). We enrolled male volunteers (≥50 yr) with an International Prostate Symptom Score (I-PSS; questions 1-7) ≥ 5 and a prostate-specific antigen (PSA) value < 4 ng/ml. Volunteers were randomized into four groups, of placebo (n= 12), and G. lucidum of 0.6 mg (n = 12), 6 mg (n=12) or 60 mg (n=14), administered once daily. Efficacy was measured as a change from baseline in I-PSS and the peak urine flow rate (Qmax). Prostate volume and residual urine were estimated by ultrasonography, and blood tests, including PSA levels, were also measured at baseline and at the end of the treatment. The overall administration was well tolerated, with no major adverse effects. Statistical significances in the magnitude of changes between the experimental groups were observed at week 4 and week 8. No changes were observed with respect to Qmax, residual urine, prostate volume or/and PSA levels. The extract of G. lucidum was well tolerated and an improvement in I-PSS was observed. The recommended dose of the extract of G. lucidum is 6 mg in men with LUTS.
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M3 - Article
AN - SCOPUS:53849124729
SN - 0029-0726
VL - 70
SP - 466
EP - 472
JO - Nishinihon Journal of Urology
JF - Nishinihon Journal of Urology
IS - 9
ER -