Wolff H, Kunte C
Klinik und Poliklinik für Dermatologie und Allergologie, Ludwig-Maximilians-Universität, München.
MMW Fortschr Med. 1999 Sep 16;141(37):38-40.
Androgenetic alopecia in men is genetically determined, but occurs only when the testosterone metabolite dihydrotestosterone (DHT) is present in normal levels. The drug, finasteride, inhibits the enzyme 5-alpha-reductase II, which is responsible for converting testosterone to DHT. One 1 mg tablet (Propecia) of finasteride daily lowers serum DHT levels by about 70%, and increases serum testosterone by 10%. The efficacy of finasteride 1 mg has been demonstrated in a randomized, double-blind, placebo-controlled clinical trial involving more than 1,500 men in whom a significant increase in hair density over a specified area of the scalp, and a significant improvement in appearance was noted. Following one year to treatment 48%, and following 2 years 66%, of the finasteride patients (placebo group 7% after both treatment periods) presented with visibly thicker hair growth. Side effects such as decreased libido, ejaculation disorders and erectile dysfunction were seen in fewer than 2% of the men in both the finasteride and placebo groups.
男性雄激素性脱发由基因决定,但仅在睾酮代谢产物双氢睾酮(DHT)处于正常水平时才会发生。非那雄胺这种药物可抑制5α-还原酶II,该酶负责将睾酮转化为DHT。每日服用一片1毫克的非那雄胺片(保法止)可使血清DHT水平降低约70%,并使血清睾酮水平升高10%。在一项涉及1500多名男性的随机、双盲、安慰剂对照临床试验中,已证实1毫克非那雄胺的疗效,该试验发现,在头皮特定区域的头发密度显著增加,外观有显著改善。治疗一年后,48%的非那雄胺患者出现明显更浓密的头发生长,治疗两年后,这一比例为66%(两个治疗期后安慰剂组均为7%)。在非那雄胺组和安慰剂组中,出现性欲减退、射精障碍和勃起功能障碍等副作用的男性均不到2%。