Sasmaz Sezai, Arican Ozer
Department of Dermatology, School of Medicine, Kahramanmaras Sutcuimam University, Kahramanmaras, Turkey.
Am J Clin Dermatol. 2005;6(6):403-6. doi: 10.2165/00128071-200506060-00007.
Although topical azelaic acid has been previously used for the treatment of alopecia, no controlled trials of azelaic acid for this condition have been conducted to date.
The goal of this study was to determine the efficacy, tolerability, and safety of azelaic acid treatment in patients with patchy alopecia areata (AA) in comparison with anthralin (dithranol) treatment.
This study included 31 subjects with patchy AA who did not receive any treatment for at least 1 month prior to the study. Demographic and clinical characteristics of these subjects were recorded at baseline. Subjects were randomized to apply either 20% azelaic acid (15 subjects) or 0.5% anthralin (16 subjects) for 12 consecutive weeks. In a subsequent 8-week follow-up period no cream was applied. Two independent investigators performed an efficacy evaluation with clinical examination using a terminal hair regrowth score (RGS) with a scale ranging from 0 (inadequate response) to 2 (complete response) at week 20. Partial response was accepted as score 1.
Both groups were well matched for the relevant demographic and clinical indicators affecting treatment response at baseline. All subjects completed the trial. At week 20 the RGS was 1.27 +/- 0.9 in the azelaic acid group versus 1.37 +/- 0.8 in the anthralin group (p > 0.05). A complete response was observed in 53.3% of cases in the azelaic acid group (8 of 15) compared with 56.2% (9 of 16) in the anthralin group (p > 0.05). No serious adverse events were observed in either group during the study.
The present pilot study showed that the use of azelaic acid gave similar results to anthralin with regard to hair regrowth, and that it can be an effective topical therapy for patchy AA. More extensive trials are necessary, however, to reach a definitive conclusion.
尽管外用壬二酸此前已用于治疗脱发,但迄今为止尚未进行过针对该病症的壬二酸对照试验。
本研究的目的是比较壬二酸与蒽林(地蒽酚)治疗斑秃(AA)患者的疗效、耐受性和安全性。
本研究纳入了31例斑秃患者,这些患者在研究前至少1个月未接受任何治疗。在基线时记录这些受试者的人口统计学和临床特征。受试者被随机分为连续12周使用20%壬二酸(15例受试者)或0.5%蒽林(16例受试者)。在随后的8周随访期内不使用任何乳膏。两名独立研究者在第20周通过临床检查进行疗效评估,使用终毛再生评分(RGS),评分范围为0(反应不足)至2(完全反应)。部分反应被接受为评分为1。
两组在基线时影响治疗反应的相关人口统计学和临床指标方面匹配良好。所有受试者均完成了试验。在第20周时,壬二酸组的RGS为1.27±0.9,而蒽林组为1.37±0.8(p>0.05)。壬二酸组53.3%的病例(15例中的8例)观察到完全反应,而蒽林组为56.2%(16例中的9例)(p>0.05)。在研究期间,两组均未观察到严重不良事件。
本初步研究表明,在毛发再生方面,使用壬二酸与蒽林的结果相似,并且它可以成为斑秃的一种有效局部治疗方法。然而,需要进行更广泛的试验才能得出明确结论。