Lueangarun Suparuj, Panchaprateep Ratchathorn
Dr. Lueangarun is with the Division of Dermatology at Chulabhorn International College of Medicine at Thammasat University in Pathumthani, Thailand.
Dr. Panchaprateep is with the Division of Dermatology, Faculty of Medicine at Chulalongkorn University, in Bangkok, Thailand.
J Clin Aesthet Dermatol. 2020 Oct;13(10):32-37. Epub 2020 Oct 1.
: We sought to evaluate the efficacy and safety profile of an herbal extract combination comprising biochanin A, acetyl tetrapeptide-3, and ginseng extracts, and compare this to 3% minoxidil solution for the treatment of andogenetic alopecia (AGA). : A 24-week, triple-blinded, randomized controlled study was conducted in male and female subjects (N=32) with mild to moderate AGA. All were randomized to receive twice-daily, 1mL applications of the herbal extract combination or 3% minoxidil solution. Clinical efficacy from photographic assessment and adverse reactions were evaluated. : There were thirty-two subjects (16 male, mean age 41.3±13.8 years), with AGA onset and duration of 35.5±13.6 and 6.5±5.1 years, respectively. The herbal extract combination demonstrated a comparable efficacy to 3% minoxidil solution. Expert panel photographic assessment observed a response to both treatments in most patients at 24 weeks, with no statistically significant difference in an increase of terminal hair counts (8.3% [=0.009] and 8.7% [=0.002] at 24 weeks in the herbal extract combinations and the 3% minoxidil solution groups, respectively). No local adverse reactions from the herbal extract combination were observed, but one subject developed scalp eczema after using the 3% minoxidil solution. : The non-significant difference in clinical efficacy and safety to 3% minoxidil solution suggests that the herbal extract combination evaluated here could potentially be an alternative treatment with for AGA. Further studies with larger groups and longer follow-up periods are recommended to verify our results.
我们旨在评估一种包含染料木黄酮、乙酰基四肽-3和人参提取物的草药提取物组合的疗效和安全性,并将其与3%米诺地尔溶液治疗雄激素性脱发(AGA)的效果进行比较。
对32名患有轻至中度AGA的男性和女性受试者进行了一项为期24周的三盲随机对照研究。所有受试者均被随机分配,每天两次,每次涂抹1mL草药提取物组合或3%米诺地尔溶液。通过照片评估临床疗效并评估不良反应。
共有32名受试者(16名男性,平均年龄41.3±13.8岁),AGA发病时间和病程分别为35.5±13.6年和6.5±5.1年。草药提取物组合显示出与3%米诺地尔溶液相当的疗效。专家小组通过照片评估发现,大多数患者在24周时对两种治疗均有反应,终毛数量增加方面无统计学显著差异(草药提取物组合组和3%米诺地尔溶液组在24周时分别为8.3%[=0.009]和8.7%[=0.002])。未观察到草药提取物组合引起的局部不良反应,但有一名受试者在使用3%米诺地尔溶液后出现头皮湿疹。
与使用3%米诺地尔溶液相比,在临床疗效和安全性方面无显著差异,这表明本文评估的草药提取物组合可能是AGA的一种替代治疗方法。建议进行更大规模人群和更长随访期的进一步研究以验证我们的结果。