School of Chemistry, Queensland University of Technology, Brisbane, QLD, Australia.
Sydney Medical School, The University of Sydney, Sydney, NSW, Australia.
Biofactors. 2017 Nov;43(6):789-800. doi: 10.1002/biof.1389. Epub 2017 Oct 19.
A double-blind, randomized, placebo-controlled clinical trial assessed the efficacy and safety of Ageratum conyzoides in treating benign prostatic hypertrophy (BPH). In this study, 109 men with medically diagnosed BPH, aged 41-76 years, were administered the investigational product, A. conyzoides extract at a dose of 250 mg/d or placebo, q.d. for 12 weeks. The primary outcome measures were the International Prostate Symptom Score (IPSS), daily urinary frequency and safety evaluations. The secondary outcome measures were testosterone, dihydrotestosterone, oestradiol, sex hormone binding globulin (SHBG), Dehydroepiandrosterone sulfate (DHEA-S) and cortisol levels, and prostate specific antigen (PSA), lipids, blood glucose, the Aging Male's Symptom (AMS) Score and sexual function assessed by Derogatis Interview for Sexual Functioning-Self Report (DISF-SR). The effect of A. conyzoides L extract on gene expression of 5-alpha-reductase in human prostate cells was also investigated to elucidate a potential mechanism of action. The clinical study, showed a significant reduction in total IPSS score (p < 0.01) and day- and night-time urinary frequency (P < 0.01) over time after treatment with A. conyzoides. Steroid hormones, SHBG, PSA levels, lipids, and blood glucose remained within healthy reference range in both groups. There were no changes in AMS or DISF-SR in either group. Gene arrays demonstrated that A. conyzoides extract was effective in reducing the expression of mRNA coding for 5-alpha-reductase types 2 and 1 in human prostate epithelial cells. The overall results indicate that A. conyzoides may be an effective treatment for reducing symptoms of BPH in healthy men, in part, through inhibition of 5-alpha-reductase enzyme activity. © 2017 BioFactors, 43(6):789-800, 2017.
一项双盲、随机、安慰剂对照的临床试验评估了穿心莲在治疗良性前列腺增生(BPH)中的疗效和安全性。在这项研究中,109 名经医学诊断患有 BPH 的 41-76 岁男性患者每天服用 250mg 的穿心莲提取物或安慰剂,qd,持续 12 周。主要疗效指标为国际前列腺症状评分(IPSS)、每日排尿频率和安全性评估。次要疗效指标为睾酮、二氢睾酮、雌二醇、性激素结合球蛋白(SHBG)、硫酸脱氢表雄酮(DHEA-S)和皮质醇水平,以及前列腺特异性抗原(PSA)、血脂、血糖、男性老化症状(AMS)评分和性功能评估采用德罗加蒂斯性功能自评问卷(DISF-SR)。还研究了穿心莲提取物对人前列腺细胞 5-α-还原酶基因表达的影响,以阐明其潜在的作用机制。临床研究表明,治疗后总 IPSS 评分(p<0.01)和白天和夜间排尿频率(P<0.01)均显著降低。两组的类固醇激素、SHBG、PSA 水平、血脂和血糖均在健康参考范围内。两组 AMS 或 DISF-SR 均无变化。基因芯片表明,穿心莲提取物能有效降低人前列腺上皮细胞中编码 5-α-还原酶 2 型和 1 型的 mRNA 表达。总的来说,穿心莲可能是一种有效的治疗方法,可减轻健康男性的 BPH 症状,部分原因是抑制 5-α-还原酶的活性。