Nong Yvonne, Sugarman Jeffrey, York Jean Philippe, Levy-Hacham Ofra, Nadora Dawnica, Mizrahi Rinat, Galati Aidan, Gallo Richard L, Sivamani Raja K
Dr. Nong is with Integrative Skin Science and Research in Sacramento, California; the Pacific Skin Institute in Sacramento, California; and the Department of Dermatology at the University of California, Davis in Sacramento, California.
Dr. Sugarman is with the University of California San Francisco in San Francisco, California.
J Clin Aesthet Dermatol. 2024 Aug;17(8):19-26.
We sought to evaluate changes in microbiome biodiversity and physical properties of the skin after eight weeks of once-daily topical microencapsulated benzoyl peroxide (E-BPO) compared to vehicle cream in participants with rosacea.
This was a randomized, double-blind, crossover, single-center, vehicle-controlled evaluation of E-BPO on the skin microbiome in rosacea. Participants had facial rosacea with global severity of 3 or 4 on the Investigator Global Assessment (IGA) scale. In the Treatment 1-2 group, participants received E-BPO for eight weeks then switched to vehicle cream for four weeks. In the Treatment 2-1 group, participants received vehicle cream for eight weeks, then E-BPO for four weeks.
Thirty-one participants were enrolled and randomly assigned to either group. Demographic characteristics were comparable between the treatment groups. After eight weeks of E-BPO treatment, there was a marked reduction in the relative abundance of accompanied by an increase in . At the species level, there was an increase in the relative abundance of and a decrease in abundance of . No noticeable difference was detected at the genus or species level at Week 8 in the 2-1 group. Sebum level, IGA, lesion counts, facial erythema, and inflammatory scores were improved with E-BPO versus vehicle cream. Adverse events were mild or moderate in severity.
The study included a small number of subjects and only surface-swabs were used for microbiome sampling.
E-BPO shifted the skin microbiome in rosacea and demonstrated improvements in clinical symptoms and skin physical properties and a well-tolerated safety profile. US National Library of Medicine; Trial ID: NCT05675501]; URL: clinicaltrials.gov.
我们试图评估与赋形剂乳膏相比,酒渣鼻患者每日一次局部使用微囊化过氧化苯甲酰(E-BPO)八周后皮肤微生物群生物多样性和物理性质的变化。
这是一项关于E-BPO对酒渣鼻皮肤微生物群的随机、双盲、交叉、单中心、赋形剂对照评估。参与者面部患有酒渣鼻,根据研究者整体评估(IGA)量表,整体严重程度为3或4级。在治疗1-2组中,参与者接受E-BPO治疗八周,然后改用赋形剂乳膏治疗四周。在治疗2-1组中,参与者接受赋形剂乳膏治疗八周,然后接受E-BPO治疗四周。
31名参与者被纳入并随机分配到两组。治疗组之间的人口统计学特征具有可比性。E-BPO治疗八周后, 的相对丰度显著降低,同时 增加。在物种水平上, 的相对丰度增加, 的丰度降低。在第8周时,2-1组在属或物种水平上未检测到明显差异。与赋形剂乳膏相比,E-BPO可改善皮脂水平、IGA、皮损计数、面部红斑和炎症评分。不良事件的严重程度为轻度或中度。
该研究纳入的受试者数量较少,且仅使用表面拭子进行微生物群采样。
E-BPO改变了酒渣鼻患者的皮肤微生物群,改善了临床症状和皮肤物理性质,且安全性良好,耐受性佳。美国国立医学图书馆;试验编号:NCT05675501];网址:clinicaltrials.gov 。