Assessing the efficacy and safety profiles of 0.025% tretinoin in treating axillary hyperpigmentation with acanthosis nigricans: a randomized double-blinded study

IF 1.8 4区 医学 Q3 DERMATOLOGY
Puri Chunekamrai, Nattasit Chatpimolkul, Soravit Thummawatwimon, Arucha Treesirichod
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Abstract

Acanthosis nigricans (AN) is a dermatological condition, marked by hyperpigmentation and skin thickening, frequently affecting body folds like the axillae. Treatment options for axillary hyperpigmentation remain underexplored. This study evaluated the efficacy of 0.025% tretinoin cream in treating axillary hyperpigmentation associated with AN. In a randomized, intra-individual, split-side design study, participants applied 0.025% tretinoin cream on one axilla and a cream-based on the other. The study spanned 12 weeks, with topical application for the first 8 weeks, followed by a 4-week cessation period. Efficacy was measured using the melanin (M) index via narrowband reflectance spectrophotometry. Overall success was evaluated through investigator- and participant-global evaluation (IGE and PGE) scales, with adverse effects monitored. Twenty participants completed the study. The 0.025% tretinoin cream significantly reduced hyperpigmentation compared to the control (p < 0.001). By week 8, the mean M index reduction with tretinoin was 28.05%±12.20%, versus 6.55%±12.66% with the control. Hyperpigmentation reappeared partially after treatment cessation. By week 8, 75% of participants in the tretinoin group achieved more than 75% improvement in IGE, compared to 35% in the cream-based group. Similarly, 75% of the tretinoin group reported more than 75% improvement in PGE, whereas only 15% of the cream-based group achieved more than 50% improvement. Adverse effects were mild and included slight erythema, peeling, and itching. The 0.025% tretinoin cream significantly improved AN patients’ axillary hyperpigmentation, demonstrating a safe and effective treatment option with minimal side effects.

评估0.025%维甲酸治疗黑棘皮病腋窝色素沉着的有效性和安全性:一项随机双盲研究
黑棘皮病(AN)是一种皮肤病,以色素沉着和皮肤增厚为特征,常影响腋窝等身体褶皱。腋窝色素沉着的治疗方案仍未得到充分探讨。本研究评估0.025%维甲酸乳膏治疗AN相关腋窝色素沉着的疗效。在一项随机、个体内部、分裂侧设计研究中,参与者在一个腋窝上涂0.025%维甲酸乳膏,在另一个腋窝上涂基于0.025%维甲酸的乳膏。该研究持续了12周,前8周局部应用,随后是4周的停药期。采用窄带反射分光光度法测定黑色素(M)指数。通过研究者和参与者整体评估(IGE和PGE)量表评估总体成功,并监测不良反应。20名参与者完成了这项研究。与对照组相比,0.025%维甲酸乳膏显著减少了色素沉着(p < 0.001)。到第8周,维甲酸组M指数平均降低28.05%±12.20%,对照组为6.55%±12.66%。停止治疗后,色素沉着部分复发。到第8周,维甲酸组75%的参与者的IGE改善超过75%,而乳霜组只有35%。同样,75%的维甲酸组报告PGE改善超过75%,而只有15%的乳霜组改善超过50%。不良反应轻微,包括轻微的红斑、脱皮和瘙痒。0.025%维甲酸乳膏可显著改善AN患者腋窝色素沉着,是一种安全有效且副作用最小的治疗选择。
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来源期刊
CiteScore
4.10
自引率
3.30%
发文量
30
审稿时长
4-8 weeks
期刊介绍: Archives of Dermatological Research is a highly rated international journal that publishes original contributions in the field of experimental dermatology, including papers on biochemistry, morphology and immunology of the skin. The journal is among the few not related to dermatological associations or belonging to respective societies which guarantees complete independence. This English-language journal also offers a platform for review articles in areas of interest for dermatologists and for publication of innovative clinical trials.
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