Draelos Zoe Diana, Peterson R Scott
J Drugs Dermatol. 2020 Jun 1;19(6):625-631. doi: 10.36849/JDD.2020.10.36849/JDD.2020.5085.
The goal of this 12 week, double-blinded, controlled, clinical study was to compare the efficacy, tolerability, and consumer acceptance of three novel retinol serums to tretinoin.
Forty-five photoaged females ages 35-65, Fitzpatrick skin types I-IV, with moderate wrinkling were enrolled in the 12-week study. A step-up protocol for increasing the dose of retinol serum (0.25%, 0.5%, 1.0%) or tretinoin cream (0.025%, 0.05%, and 0.1%) in combination with a test moisturizer or currently marketed dermatologist-recommended moisturizing cream was used. Overall severity of investigator graded photodamage, subject assessed photodamage, and tolerability criteria were evaluated using a 5-point ordinal scale at weeks 4, 8, and 12. Facial photography occurred at each visit and TEWL was measured at baseline and week 12. Histologic evaluation of punch biopsies was completed on baseline and week 12 samples.
After 12 weeks of use, both retinol serum and tretinoin demonstrated parity across investigator and subject assessment measurements as well as diagnostic measures including TEWL. Retinol serum subjects showed significant week 4 improvement in visual skin smoothness compared to tretinoin subjects (P=0.031). There was highly significant improvement in skin dryness with the retinol serum (P<0.001) not seen in the tretinoin group. Histologic analysis of baseline and 12-week punch biopsies demonstrated newly formed collagen and greater epidermal thickening in retinol serum subjects compared to tretinoin treated subjects.
Retinol serum (0.25%, 0.5%, 1.0%) was safe and effective with equivalent/or better performance and tolerability than tretinoin creams. J Drugs Dermatol. 2020;19(6): doi:10.36849/JDD.2020.5085.
这项为期12周的双盲、对照临床研究的目的是比较三种新型视黄醇血清与维甲酸的疗效、耐受性和消费者接受度。
45名年龄在35 - 65岁、Fitzpatrick皮肤类型为I - IV型、有中度皱纹的光老化女性参加了这项为期12周的研究。采用逐步递增方案,增加视黄醇血清(0.25%、0.5%、1.0%)或维甲酸乳膏(0.025%、0.05%和0.1%)的剂量,并联合使用测试保湿霜或目前市场上皮肤科医生推荐的保湿霜。在第4、8和12周,使用5分序数量表评估研究者分级的光损伤总体严重程度、受试者评估的光损伤以及耐受性标准。每次就诊时进行面部摄影,并在基线和第12周测量经皮水分流失(TEWL)。对基线和第12周的打孔活检样本进行组织学评估。
使用12周后,视黄醇血清和维甲酸在研究者和受试者评估测量以及包括TEWL在内的诊断测量方面表现相当。与维甲酸组相比,视黄醇血清组受试者在第4周时视觉皮肤光滑度有显著改善(P = 0.031)。视黄醇血清组皮肤干燥情况有极显著改善(P < 0.001),而维甲酸组未观察到这种情况。与维甲酸治疗组相比,视黄醇血清组基线和第12周打孔活检的组织学分析显示有新形成的胶原蛋白,且表皮增厚更明显。
视黄醇血清(0.25%、0.5%、1.0%)安全有效,其性能和耐受性等同于/优于维甲酸乳膏。《药物皮肤病学杂志》。2020年;19(6):doi:10.36849/JDD.2020.5085 。